Recall events
/
Event 79619
Event summary
Timeline bucket March 22, 2018
Product types Drug
Classifications Class II
Statuses Terminated
Recalling firm wording Partell Specialty Pharmacy
Dossier provenance
Source snapshots represented here
openFDA Drug Enforcement
Report-date coverage
June 20, 2012–July 08, 2026
Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.
How coverage and grouping work
Device root-cause evidence is not applicable to this event.
No grouped product has the official product type device; this is not an unavailable-enrichment finding.
Complete imported group
Every recalled product in this event
49 official enforcement rows
Product dates, classifications, firms, and source wording remain attached to their individual rows.
Opening this dossier never hides products that did not match a prior timeline filter.
drug · product 1 of 49
Ascorbic Acid (Tapioca) 500 mg/mL, 50 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
D-0634-2018
Recall number D-0634-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity 4 vials
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20180201@34, BUD 04/02/2018; 20180202@56, BUD 04/03/2018; 20180129@41, BUD 3/30/2018; 20180207@16, BUD 04/08/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[2112]
FDA event record
· Exact recall-number query on openFDA
drug · product 2 of 49
B-complex (B1-200mg, B2-4mg, B3-200mg,B5-4mg,B6-4mg) /mL, 5 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
D-0635-2018
Recall number D-0635-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity 5 vials
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20180205@18, BUD 04/06/2018; 20180126@28, BUD 03/27/2018; 20180126@22, BUD 03/27/2018; 20180205@9, BUD 04/06/2018; 20180214@17, BUD 04/14/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[1628]
FDA event record
· Exact recall-number query on openFDA
drug · product 3 of 49
Biotin Suspension 10mg/mL, 5 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
D-0636-2018
Recall number D-0636-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity 2 vials
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot #:20180216@10, BUD 5/17/2018; 20180129@25, BUD 04/29/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[2144]
FDA event record
· Exact recall-number query on openFDA
drug · product 4 of 49
CoEnzymeQ10 25mg/mL, 5mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800.
D-0637-2018
Recall number D-0637-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity 3 vials
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20171227@14, BUD 03/27/2018; 20180205@37, BUD 05/06/2018; 20180214@30, BUD 05/15/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[1625]
FDA event record
· Exact recall-number query on openFDA
drug · product 5 of 49
Glutathione 200mg/mL, 10mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
D-0638-2018
Recall number D-0638-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity four vials
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20180219@58, BUD 05/20/2018; 20180131@15, BUD 05/01/2018; 20180116@9, BUD 04/14/2018; 20180103@5, BUD 04/03/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[2581]
FDA event record
· Exact recall-number query on openFDA
drug · product 6 of 49
HCG 1000 units/mL, packaged in a) 2 mL and b) 6 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
D-0639-2018
Recall number D-0639-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity four vials
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information a) Lot#: 20180219@6, BUD 04/05/2018; b) 20180207@14, BUD 03/24/2018; 0180214@22, BUD 03/31/2018; 20180220@7, BUD 04/06/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[2174]
FDA event record
· Exact recall-number query on openFDA
drug · product 7 of 49
Lipoic Acid 25mg/mL, 5 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
D-0640-2018
Recall number D-0640-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20180124@10, BUD 04/05/2018; 20180220@9, BUD 05/21/2018; 20180102@33, BUD 04/02/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[2143]
FDA event record
· Exact recall-number query on openFDA
drug · product 8 of 49
Methionine15mg/Inositol 50mg/Choline 100mg, packaged in a) 5mL and b) 50 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
D-0641-2018
Recall number D-0641-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity 11 vials
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information a) Lot #: 20180129@18, BUD 4/14/2018 b) Lot #: 20171127@6, 20180207@12, 20180108@16, BUD 04/14/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[1779]
FDA event record
· Exact recall-number query on openFDA
drug · product 9 of 49
Methionine 25mg/Inositol 50mg/Choline 50mg/ B12 1mg, packaged in a) 5 mL amber vial and b) 50mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
D-0642-2018
Recall number D-0642-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information a) Lot #: 20180123@9, 20171222@11, BUD 4/14/2018, 20180214@7, BUD 08/14/2018. b) Lot #: 20180221@3,BUD 08/21/2018, 20180214@6; BUD 08/14/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[1660]
FDA event record
· Exact recall-number query on openFDA
drug · product 10 of 49
Nandrolone decanoate 200mg/mL, 5 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
D-0643-2018
Recall number D-0643-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity 2 vials
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20180221@15, BUD 05/22/2018, 20180123@10, BUD 04/23/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[1399]
FDA event record
· Exact recall-number query on openFDA
drug · product 11 of 49
Testosterone Cypionate 200mg/mL, 5 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
D-0644-2018
Recall number D-0644-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity 7 vials
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot #: 20180130@2, BUD 7/29/2018; 20180109@1, BUD 07/08/2018; 20180212@51, BUD 08/11/2018;, 20171212@4, BUD 06/10/2018; 20180123@6, BUD 07/22/2018; 20171204@4, BUD 06/02/2018; 20171228@15, BUD 03/28/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[1794]
FDA event record
· Exact recall-number query on openFDA
drug · product 12 of 49
TM #1 (ALP 5.9/PAPAV 17.65/PHEN 0.59) Injectable solution, packaged in 3 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
D-0645-2018
Recall number D-0645-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity 15 vials
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20180212@22, BUD 03/29/2018; 20180226@64, BUD 04/02/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[4136]
FDA event record
· Exact recall-number query on openFDA
drug · product 13 of 49
Vitamin D 50,000 unit/ml, 5 mL amber vial, Injectable Liquid, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. # 101, Las Vegas, NV 89119 (702) 791-3800
D-0646-2018
Recall number D-0646-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity 4 vials
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20180220@4, BUD 03/22/2018, 20180221@14, BUD 03/23/2018, 20180228@1, BUD 03/30/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[1452]
FDA event record
· Exact recall-number query on openFDA
drug · product 14 of 49
Methionine 25mg/Inositol 50mg/Choline 50mg/ B12 1mg, 50 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
D-0647-2018
Recall number D-0647-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity 1 vial
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot #: 20180123@4, BUD 4/14/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[1450]
FDA event record
· Exact recall-number query on openFDA
drug · product 15 of 49
Naltrexone 200 mg pellet, amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
D-0648-2018
Recall number D-0648-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20180219@90, BUD 08/18/2018
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[4124]
FDA event record
· Exact recall-number query on openFDA
drug · product 16 of 49
Pregnenolone 100 mg (SD) pellet, amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
D-0649-2018
Recall number D-0649-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity one vial
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20171017@85, BUD: 04/15/2018
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[2132]
FDA event record
· Exact recall-number query on openFDA
drug · product 17 of 49
Progesterone 50 mg (SD) pellets in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800 twist top surrounded by a wrapper,
D-0650-2018
Recall number D-0650-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity five vials
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20171220@10, BUD 06/18/201; 20171017@83, BUD 04/15/2018; 20171102@40, BUD 05/01/2018; 20180118@97, BUD 07/17/2018; 00180213@32, BUD 08/12/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[1654]
FDA event record
· Exact recall-number query on openFDA
drug · product 18 of 49
Testosterone/Anastrozole 120 mg/8 mg pellets packaged in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
D-0651-2018
Recall number D-0651-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20171220@11, BUD 06/18/2018; 20180201@33, BUD 07/31/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[2165]
FDA event record
· Exact recall-number query on openFDA
drug · product 19 of 49
Testosterone/Estradiol 60 mg/6 mg pellet Amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800 Testosterone/Finasteride 60 mg/5 mg pellet Amber vial, twist top surrounded by a wrapper Testosterone/Finasteride 80mg/8mg pellet Amber vial, twist top surrounded by a wrapper Testosterone/Finasteride/Anastrozole 120 mg/10 mg/4 mg pellet Amber vial, twist top surrounded by a wrapper
D-0652-2018
Recall number D-0652-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity 1 vial
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20171010@76, BUD: 04/08/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[1477]
FDA event record
· Exact recall-number query on openFDA
drug · product 20 of 49
Testosterone/Finasteride 60 mg/5 mg pellet Amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
D-0653-2018
Recall number D-0653-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity 7 vials
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20171012@63, BUD 04/10/2018, 20171127@103, BUD 05/26/2018, 20180115@69, BUD 07/14/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[2587]
FDA event record
· Exact recall-number query on openFDA
drug · product 21 of 49
Testosterone/Finasteride/Anastrozole 120 mg/10 mg/4 mg pellet Amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
D-0654-2018
Recall number D-0654-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity one vial
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20180111@104, BUD 07/10/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[1473]
FDA event record
· Exact recall-number query on openFDA
drug · product 22 of 49
Methylcobalamin 12.5 mg/mL, Injectable Liquid, packaged in a) 5 mL amber vial, and b) 50 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
D-0655-2018
Recall number D-0655-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: a) 20180119@4, 20171016@10, 20171106@5, 20171214@55, 20180207@5 BUD 04/14/2018; 20180212@15, BUD 03/29/2018; 20180117@26, BUD 07/16/2018. b) 20180219@17, BUD 08/18/2018; 20180205@1, 20180102@39, 20180124@3, BUD 04/14/2018; 20180221@23, BUD 08/20/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[1411]
FDA event record
· Exact recall-number query on openFDA
drug · product 23 of 49
MVI-7 (B1-100mg/B3-100mg, B5-252 mg, B6-102mg, Vit C-2500 mg, B12-10mg, Mag-1000 mg)/ vial liquid injectable, 50 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
D-0656-2018
Recall number D-0656-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot #: 20180223@1, BUD 04/24/2018; 20180129@5, BUD 03/30/2018; 20180126@4, BUD 03/27/2018; 20180215@22, BUD 04/16/2018; 20180122@10, 20180126@4, BUD 03/23/2018; 20180202@27, BUD 04/03/2018; 20180208@5, 20180201@2, BUD 04/02/2018; # 20180207@2, BUD 04/08/2018, 20180214@11, BUD 04/15/2018; 20180215@22, BUD 04/16/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[2545]
FDA event record
· Exact recall-number query on openFDA
drug · product 24 of 49
Testosterone Propionate 100mg/mL, 5 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
D-0657-2018
Recall number D-0657-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot #: 20171228@15, BUD 03/28/2018
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[1316]
FDA event record
· Exact recall-number query on openFDA
drug · product 25 of 49
TM #4 (ALP 20/PAPAV/PHENT 2), 3 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
D-0658-2018
Recall number D-0658-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20180219@27, 20180212@18, BUD 04/02/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[1662]
FDA event record
· Exact recall-number query on openFDA
drug · product 26 of 49
TM #6 (ALP 25/PAPAV/PHENT1), 3 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
D-0659-2018
Recall number D-0659-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20180206@7, BUD 03/23/2018, 20180212@41, BUD 03/29/2018, 20180219@40, BUD 04/02/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[2130]
FDA event record
· Exact recall-number query on openFDA
drug · product 27 of 49
TM (ALP 50/PAPAV 30/PHENT1.5 mg), 3 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
D-0660-2018
Recall number D-0660-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20180219@31, BUD 04/02/2018; 20180212@42, 20180206@12, BUD 03/29/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[2561]
FDA event record
· Exact recall-number query on openFDA
drug · product 28 of 49
TM #3 (ALP10/PAPAV12/PHENT1), 3 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
D-0661-2018
Recall number D-0661-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20180206@3, BUD 03/23/2018; 20180212@15, BUD 03/29/2018, 20180219@16, BUD 04/02/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[2235]
FDA event record
· Exact recall-number query on openFDA
drug · product 29 of 49
Testosterone 200 mg pellet packaged in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3
D-0662-2018
Recall number D-0662-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20171128@9, BUD 05/27/2018; 20171201@74, BUD 05/30/2018; 20171211@68, BUD 06/09/2018; 20171218@51, BUD 06/16/2018; 20171222@6, BUD 06/20/2018; 20180209@62, BUD 08/08/2018; 20180223@46, BUD 08/22/2018; 20180223@33, BUD 08/22/2018; 20180219@5, BUD 08/18/2018; 20171010@11, BUD 04/08/2018; 20171019@19, BUD 04/17/2018; 20171031@69, BUD 04/29/2018; 20171102@27, BUD 05/01/2018; 20171110@87, BUD 05/09/2018; 20171114@12, BUD 05/13/2018; 20171122@57, BUD 05/21/2018; 20180112@56, BUD 07/11/2018; 20180116@77, BUD 07/15/2018; 20180122@92, BUD 07/21/2018; 20180202@69, BUD 08/01/2018; 20180205@111, BUD 08/04/2018; 20180212@102, BUD 08/11/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[2187]
FDA event record
· Exact recall-number query on openFDA
drug · product 30 of 49
Testosterone 100 mg pellet packaged in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
D-0663-2018
Recall number D-0663-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20171212@17, BUD 06/10/2018; 20180205@40, BUD 08/04/2018; 20180208@42, BUD 08/07/2018; 20170929@42, BUD 03/28/2018; 20171013@33, BUD 04/11/2018; 20171020@25, BUD 04/18/2018; 20171025@52, BUD 04/23/2018; 20171101@70, BUD 04/30/2018; 20171106@31, BUD 05/05/2018; 20171116@17, BUD: 05/15/2018, 20171116@42, BUD 05/15/2018; 20180117@87, BUD: 07/16/2018; 20180201@76, BUD 07/31/2018; 20180220@67, BUD 08/19/2018; 20180202@67, BUD 08/01/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[1774]
FDA event record
· Exact recall-number query on openFDA
drug · product 31 of 49
Testosterone 25 mg pellet packaged in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
D-0664-2018
Recall number D-0664-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20180130@61, BUD 07/29/2018; 20180208@17, BUD 08/07/2018, 20170928@27, BUD 03/27/2018; 20171025@49, BUD 04/23/2018; 20171109@42, BUD 05/08/2018; 20171117@1, BUD 05/16/2018; 20180130@96, BUD 07/29/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[1768]
FDA event record
· Exact recall-number query on openFDA
drug · product 32 of 49
Testosterone 37.5 mg pellet packaged in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
D-0665-2018
Recall number D-0665-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20180220@87, BUD 08/19/2018; 20171113@80, BUD 05/12/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[2154]
FDA event record
· Exact recall-number query on openFDA
drug · product 33 of 49
Testosterone 40 mg pellet packaged in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
D-0666-2018
Recall number D-0666-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20171214@90, BUD 06/12/2018; 20171113@81, BUD 05/12/2018; 20180220@58, BUD 08/19/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[2590]
FDA event record
· Exact recall-number query on openFDA
drug · product 34 of 49
Testosterone 50 mg pellet packaged in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
D-0667-2018
Recall number D-0667-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#:0180126@48, BUD 07/25/2018; 20171109@48, BUD 05/08/2018
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[1469]
FDA event record
· Exact recall-number query on openFDA
drug · product 35 of 49
Testosterone 55 mg pellet packaged in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
D-0668-2018
Recall number D-0668-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20171024@53, BUD 04/22/2018; 20180219@91, BUD 08/18/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[1458]
FDA event record
· Exact recall-number query on openFDA
drug · product 36 of 49
Testosterone 80 mg pellet packaged in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
D-0669-2018
Recall number D-0669-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20171213@93, BUD 06/11/2018; 20171220@78, BUD 06/18/2018; 20171017@41, BUD 04/15/2018; 20171117@2, BUD 05/16/2018; 20171213@93, BUD 06/11/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[2577]
FDA event record
· Exact recall-number query on openFDA
drug · product 37 of 49
Testosterone/Anastrozole 200 mg/20 mg pellets packaged in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800.
D-0670-2018
Recall number D-0670-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20171116@3, BUD 05/15/2018; 20180221@72, BUD, 08/20/2018; 20171130@79, BUD 05/29/2018; 20180221@72, BUD 08/20/2018; 20180206@115, BUD 08/05/2018; 20171023@98, BUD 04/21/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[2129]
FDA event record
· Exact recall-number query on openFDA
drug · product 38 of 49
Testosterone/Anastrozole 60 mg/1 mg pellets packaged in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800.
D-0671-2018
Recall number D-0671-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20171130@64, BUD 05/29/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[1641]
FDA event record
· Exact recall-number query on openFDA
drug · product 39 of 49
Testosterone/Anastrozole 60 mg/4 mg pellets packaged in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800.
D-0672-2018
Recall number D-0672-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20171122@65, BUD 05/21/2018; 20171115@56, BUD 05/14/2018; 20171002@77, BUD 03/31/2018; 20171006@63, BUD 04/04/2018; 20171009@55, BUD 04/07/2018; 20171117@72, BUD 05/16/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[1327]
FDA event record
· Exact recall-number query on openFDA
drug · product 40 of 49
Estradiol 10 mg (SD) pellets in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800.
D-0673-2018
Recall number D-0673-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20171201@84, BUD: 05/30/2018; 20180125@31, BUD 07/24/2018; 20180209@106, BUD 08/08/2018; 20171011@69, BUD 04/09/2018; 20171019@10, BUD 04/17/2018; 20171106@103, BUD 05/05/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[2179]
FDA event record
· Exact recall-number query on openFDA
drug · product 41 of 49
Estradiol 12.5 mg (SD) pellets in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800.
D-0674-2018
Recall number D-0674-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information a) Lot#: 20180219@88, 20180208@19, 20180219@45, BUD 08/18/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[2125]
FDA event record
· Exact recall-number query on openFDA
drug · product 42 of 49
Estradiol 15 mg (SD) pellets in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800.
D-0675-2018
Recall number D-0675-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20171204@117, BUD 06/02/2018; 20180129@14, BUD 07/28/2018; 20171011@111, BUD 04/09/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[2555]
FDA event record
· Exact recall-number query on openFDA
drug · product 43 of 49
Estradiol 20 mg (SD) pellets in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800.
D-0676-2018
Recall number D-0676-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20180129@15, BUD 07/28/2018; 20171207@83, BUD 06/05/2018; 20171016@27, BUD 04/14/2018; 20171204@15, BUD 06/02/2018; 20171006@57, BUD 04/04/2018; 20171018@62, BUD 04/16/2018; 20180116@24, BUD 07/15/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[1455]
FDA event record
· Exact recall-number query on openFDA
drug · product 44 of 49
Estradiol 25 mg (SD) pellets in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800.
D-0677-2018
Recall number D-0677-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20171204@15, BUD 06/02/2018; 20171006@57, BUD 04/04/2018; 20171018@62, BUD 04/16/2018; 20180116@24, BUD 07/15/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[1382]
FDA event record
· Exact recall-number query on openFDA
drug · product 45 of 49
Estradiol 35 mg (SD) pellets in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800.
D-0678-2018
Recall number D-0678-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot: #20171102@42, BUD 05/01/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[2208]
FDA event record
· Exact recall-number query on openFDA
drug · product 46 of 49
Estradiol 40 mg (SD) pellets in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800.
D-0679-2018
Recall number D-0679-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20171017@87, BUD 04/15/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[2114]
FDA event record
· Exact recall-number query on openFDA
drug · product 47 of 49
Estradiol 50 mg (SD) pellets in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800.
D-0680-2018
Recall number D-0680-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20171009@49, BUD 04/07/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[1463]
FDA event record
· Exact recall-number query on openFDA
drug · product 48 of 49
Estradiol 55 mg (SD) pellets in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800.
D-0681-2018
Recall number D-0681-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information Lot#: 20180104@73, BUD 07/03/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[1319]
FDA event record
· Exact recall-number query on openFDA
drug · product 49 of 49
Testosterone/Finasteride 80 mg/8 mg pellet, amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800.
D-0682-2018
Recall number D-0682-2018
Initiated March 22, 2018
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Code information 20180110@57, 20180110@23 BUD 07/09/2018, 20171003@91, BUD 04/01/2018, 20171016@24, BUD 04/14/2018.
Distribution pattern NV only
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[2559]
FDA event record
· Exact recall-number query on openFDA
