Recall events
/
Event 82941
Event summary
Timeline bucket May 23, 2019
Product types Drug
Classifications Class II
Statuses Terminated
Recalling firm wording Pharm D Solutions, LLC
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
18 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 18
Bacteriostatic Water for Injection, 10 mL vials, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846
D-1322-2019
Recall number D-1322-2019
Initiated May 23, 2019
Classification Class II
Status Terminated
Quantity 716 vials
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of Sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Sterility Assurance.
Code information Lot #: 11292018:75 Exp. 05/28/2019; 01022019:70 Exp. 07/01/2019; 02042019:04 Exp. 08/03/2019; 03042019:94 Exp. 08/31/2019
Distribution pattern Nationwide within the United States
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[10559]
FDA event record
· Exact recall-number query on openFDA
drug · product 2 of 18
B-complex (Thiamine 100mg, Riboflavin 2mg, Niacinamide 100 mg, Pyridoxine 2mg, Depanthenol 5mg) injectable, 10 mL vials, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846, NDC 69699-1611-30
D-1323-2019
Recall number D-1323-2019
Initiated May 23, 2019
Classification Class II
Status Terminated
Quantity 4 vials
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of Sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Sterility Assurance.
Code information Lot #: 04032019:23 Exp. 06/11/2019
Distribution pattern Nationwide within the United States
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[11225]
FDA event record
· Exact recall-number query on openFDA
drug · product 3 of 18
Human Chorionic Gonadotropin 10,000 IU vials, Rx only Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846
D-1324-2019
Recall number D-1324-2019
Initiated May 23, 2019
Classification Class II
Status Terminated
Quantity 26 vails
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of Sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Sterility Assurance.
Code information Lot #: 02052019:42 Exp. 08/03/2019
Distribution pattern Nationwide within the United States
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[10925]
FDA event record
· Exact recall-number query on openFDA
drug · product 4 of 18
Human Chorionic Gonadotropin 5,000 IU vials, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846
D-1325-2019
Recall number D-1325-2019
Initiated May 23, 2019
Classification Class II
Status Terminated
Quantity 279 vials
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of Sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Sterility Assurance.
Code information Lot #: 01082019:88 Exp. 07/06/2019; 03182019:58 Exp. 09/14/2019
Distribution pattern Nationwide within the United States
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[11233]
FDA event record
· Exact recall-number query on openFDA
drug · product 5 of 18
Human Chorionic Gonadotropin 12,000 IU vials Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846
D-1326-2019
Recall number D-1326-2019
Initiated May 23, 2019
Classification Class II
Status Terminated
Quantity 104 vials
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of Sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Sterility Assurance.
Code information Lot #: 01232019:86 Exp. 07/22/2019; 04042019:86 Exp. 10/01/2019
Distribution pattern Nationwide within the United States
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[10962]
FDA event record
· Exact recall-number query on openFDA
drug · product 6 of 18
Ipamorelin Acetate 9 mg/9mL Injectable vials, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846
D-1327-2019
Recall number D-1327-2019
Initiated May 23, 2019
Classification Class II
Status Terminated
Quantity 11 vials
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of Sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Sterility Assurance.
Code information Lot #: 05022019:50 Exp. 10/29/2019; 05082019:91 Exp. 06/08/2019
Distribution pattern Nationwide within the United States
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[11250]
FDA event record
· Exact recall-number query on openFDA
drug · product 7 of 18
Lipo MIC-12 (Methylcobalamin, USP 1mg, Methionine USP 15mg, Inositol, FCC 50mg, Choline Chloride, FCC 100 mg) 10 mL Injectable vials, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846
D-1328-2019
Recall number D-1328-2019
Initiated May 23, 2019
Classification Class II
Status Terminated
Quantity 669 vials
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of Sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Sterility Assurance.
Code information Lot #: 02202019:53/A Exp. 08/18/2019; 04012019:67/A, 04022019:47/A Exp. 09/28/2019; 04042019:04/A Exp. 09/30/2019; 04082019:38/A Exp. 10/02/2019; 04302019:49/A Exp. 10/27/2019; 05062019:09 Exp. 11/02/2019
Distribution pattern Nationwide within the United States
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[11201]
FDA event record
· Exact recall-number query on openFDA
drug · product 8 of 18
Nandrolone Decanoate 200 mg/mL Injectable, 10 mL vials, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846
D-1329-2019
Recall number D-1329-2019
Initiated May 23, 2019
Classification Class II
Status Terminated
Quantity 50 vials
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of Sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Sterility Assurance.
Code information Lot #: 01312019:34 Exp. 07/30/2019
Distribution pattern Nationwide within the United States
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[11044]
FDA event record
· Exact recall-number query on openFDA
drug · product 9 of 18
Sermorelin/Ipamorelin 18 mg/15 mg, 10mL vials, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846
D-1330-2019
Recall number D-1330-2019
Initiated May 23, 2019
Classification Class II
Status Terminated
Quantity 24 vials
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of Sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Sterility Assurance.
Code information Lot #: 04162019:48 Exp. 10/13/2019; 04302019:70 Exp. 10/27/2019; 05022019:34 Exp. 10/29/2019
Distribution pattern Nationwide within the United States
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[11215]
FDA event record
· Exact recall-number query on openFDA
drug · product 10 of 18
Sermorelin/GHRP-2 9 mg/9 mg vials Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846
D-1331-2019
Recall number D-1331-2019
Initiated May 23, 2019
Classification Class II
Status Terminated
Quantity 6 vials
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of Sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Sterility Assurance.
Code information Lot #: 05082019:92 Exp. 06/04/2019
Distribution pattern Nationwide within the United States
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[11261]
FDA event record
· Exact recall-number query on openFDA
drug · product 11 of 18
Sermorelin/GHRP-2 9 mg/6 mg vials, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846
D-1332-2019
Recall number D-1332-2019
Initiated May 23, 2019
Classification Class II
Status Terminated
Quantity 66 vials
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of Sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Sterility Assurance.
Code information Lot #: 03052019:43 Exp. 08/31/2019; 04042019:15 Exp. 10/01/2019; 04172019:08 Exp. 08/31/2019; 05022019:47 Exp. 10/30/2019; 05082019:78 Exp. 06/04/2019
Distribution pattern Nationwide within the United States
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[11253]
FDA event record
· Exact recall-number query on openFDA
drug · product 12 of 18
Sermorelin/GHRP-2 & 6 (3-3-3 MG) vials, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846
D-1333-2019
Recall number D-1333-2019
Initiated May 23, 2019
Classification Class II
Status Terminated
Quantity 100 vials
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of Sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Sterility Assurance.
Code information Lot #: 12062018:17 Exp. 06/04/2019
Distribution pattern Nationwide within the United States
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[11228]
FDA event record
· Exact recall-number query on openFDA
drug · product 13 of 18
Sermorelin/GHRP-2 &6 (9-9-9-mg) vials, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846
D-1334-2019
Recall number D-1334-2019
Initiated May 23, 2019
Classification Class II
Status Terminated
Quantity 1 vial
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of Sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Sterility Assurance.
Code information Lot #: 05032019:29 Exp. 11/02/2019
Distribution pattern Nationwide within the United States
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[11258]
FDA event record
· Exact recall-number query on openFDA
drug · product 14 of 18
Sermorelin/GHRP-2 &6 (9-9-9 mg) vials, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846
D-1335-2019
Recall number D-1335-2019
Initiated May 23, 2019
Classification Class II
Status Terminated
Quantity 25 vials
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of Sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Sterility Assurance.
Code information Lot #: 02182019:79 Exp. 08/17/2019; 04162019:86 Exp. 10/13/2019
Distribution pattern Nationwide within the United States
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[11220]
FDA event record
· Exact recall-number query on openFDA
drug · product 15 of 18
Testosterone 200 mg/mL, 30 mL vials, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846, NDC 69699-1702-30
D-1336-2019
Recall number D-1336-2019
Initiated May 23, 2019
Classification Class II
Status Terminated
Quantity 704 vials
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of Sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Sterility Assurance.
Code information Lot #: 10242018:70/B Exp. 08/31/2019; 10302018:63/A Exp. 08/31/2019
Distribution pattern Nationwide within the United States
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[11240]
FDA event record
· Exact recall-number query on openFDA
drug · product 16 of 18
Testosterone Cyp/Pro 95/5%, 10 mL vials, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846
D-1337-2019
Recall number D-1337-2019
Initiated May 23, 2019
Classification Class II
Status Terminated
Quantity 371 vials
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of Sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Sterility Assurance.
Code information Lot #: 01312019:02 Exp. 08/16/2019; 02072019:45/A Exp. 11/30/2019
Distribution pattern Nationwide within the United States
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[11199]
FDA event record
· Exact recall-number query on openFDA
drug · product 17 of 18
Testosterone Cypionate 200 mg/mL, in a) 5mL vials and b)10 mL vials, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846, NDC 69699-1702-10
D-1338-2019
Recall number D-1338-2019
Initiated May 23, 2019
Classification Class II
Status Terminated
Quantity a) 114 vials and b) 566 vials
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of Sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Sterility Assurance.
Code information Lot #: a) 10242018:70/P, Exp. 08/31/2019; b) 10242018:70/A Exp. 08/31/2019; 02262019:49/A Exp. 11/30/2019
Distribution pattern Nationwide within the United States
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[11229]
FDA event record
· Exact recall-number query on openFDA
drug · product 18 of 18
Trimix 30mg/1 mg/10mcg/mL ( 30 mg Papaverine, 1mg phentolamine mesylate, 30 mcg alprostadil) Injectable, 5mL vials, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846
D-1339-2019
Recall number D-1339-2019
Initiated May 23, 2019
Classification Class II
Status Terminated
Quantity 4 vials
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of Sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Sterility Assurance.
Code information Lot #: 05022019:90 Exp. 07/13/2019
Distribution pattern Nationwide within the United States
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[11239]
FDA event record
· Exact recall-number query on openFDA
