Recall events
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Event 83397
Event summary
Timeline bucket July 22, 2019
Product types Drug
Classifications Class II
Statuses Terminated
Recalling firm wording Wise 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
11 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 11
Acetylcysteine 2% Otic Drop, 15 mL bottle, Rx only, Refrigerate, Compounded by Wise Pharmacy, Littleton, CO 80123.
D-1567-2019
Recall number D-1567-2019
Initiated July 22, 2019
Classification Class II
Status Terminated
Quantity 1 bottle
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
Lack of Processing Controls
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Processing Controls
Code information Lot #: 7131N, Exp 7/11/19
Distribution pattern CO, TX, WY
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[11539]
FDA event record
· Exact recall-number query on openFDA
drug · product 2 of 11
Alprostadil 100 mcg/mL Injectable, 2.5 mL vial, Rx only, Compounded by Wise Pharmacy, Littleton, CO 80123.
D-1568-2019
Recall number D-1568-2019
Initiated July 22, 2019
Classification Class II
Status Terminated
Quantity 4 vials
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
Lack of Processing Controls
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Processing Controls
Code information Lot #: 6981N, Exp 10/17/2019
Distribution pattern CO, TX, WY
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[11464]
FDA event record
· Exact recall-number query on openFDA
drug · product 3 of 11
Dexamethasone Sodium Phosphate PF 24 mg/mL Injection, Refrigerate, Single Use Vial, 1 mL vial, Rx only, Compounded by Wise Pharmacy, Littleton, CO 80123.
D-1569-2019
Recall number D-1569-2019
Initiated July 22, 2019
Classification Class II
Status Terminated
Quantity 27 vials
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
Lack of Processing Controls
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Processing Controls
Code information Lots #: 5506N, Exp 9/21/2019; 7180N, Exp 12/29/2019
Distribution pattern CO, TX, WY
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[11608]
FDA event record
· Exact recall-number query on openFDA
drug · product 4 of 11
Gentamicin (GU) Irrigation 240 mg/500 mL Solution, 250 mL Container, Shake well and Refrigerate, Rx only, Compounded by Wise Pharmacy, Littleton, CO 80123.
D-1570-2019
Recall number D-1570-2019
Initiated July 22, 2019
Classification Class II
Status Terminated
Quantity 1 container
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
Lack of Processing Controls
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Processing Controls
Code information Lot #: 7179N, Exp 7/16/2019
Distribution pattern CO, TX, WY
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[11619]
FDA event record
· Exact recall-number query on openFDA
drug · product 5 of 11
Tobramycin Irrigation 80 mg/1000 mL Solution, 1000 mL Container, Refrigerate, Nasal,, Rx only, Compounded by Wise Pharmacy, Littleton, CO 80123.
D-1571-2019
Recall number D-1571-2019
Initiated July 22, 2019
Classification Class II
Status Terminated
Quantity 1 container
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
Lack of Processing Controls
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Processing Controls
Code information Lot #: 7270N, Exp 7/22/2019
Distribution pattern CO, TX, WY
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[11550]
FDA event record
· Exact recall-number query on openFDA
drug · product 6 of 11
Papaverine/Phentolamine 30 mg/1 mg/mL Injectable, 2.5 mL Vial, Rx only, Compounded by Wise Pharmacy, Littleton, CO 80123.
D-1572-2019
Recall number D-1572-2019
Initiated July 22, 2019
Classification Class II
Status Terminated
Quantity 8 vials
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
Lack of Processing Controls
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Processing Controls
Code information Lot #: 5978N, Exp 8/20/2019; 7266N, Exp 11/5/2019
Distribution pattern CO, TX, WY
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[11548]
FDA event record
· Exact recall-number query on openFDA
drug · product 7 of 11
Papaverine/Phentolamine/Alprostadil 30 mg/0.2 mg/10 mcg/mL Injectable, 2.5 mL Vial, Rx only, Compounded by Wise Pharmacy, Littleton, CO 80123.
D-1573-2019
Recall number D-1573-2019
Initiated July 22, 2019
Classification Class II
Status Terminated
Quantity 84 vials
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
Lack of Processing Controls
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Processing Controls
Code information Lot #: 6054N; 4796N, Exp 7/16/2019; 7049N, Exp 11/24/2019
Distribution pattern CO, TX, WY
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[11162]
FDA event record
· Exact recall-number query on openFDA
drug · product 8 of 11
Papaverine/Phentolamine/Alprostadil - 30 mg/1 mg/10 mcg/mL Injectable, 2.5 mL Vial, Rx only, Compounded by Wise Pharmacy, Littleton, CO 80123.
D-1574-2019
Recall number D-1574-2019
Initiated July 22, 2019
Classification Class II
Status Terminated
Quantity 44 vials
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
Lack of Processing Controls
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Processing Controls
Code information Lot #: 5333N, Exp 7/12/2019; 7000N, Exp 10/18/2019
Distribution pattern CO, TX, WY
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[11452]
FDA event record
· Exact recall-number query on openFDA
drug · product 9 of 11
Papaverine/Phentolamine/Alprostadil 30 mg/2 mg/30 mcg/mL Injectable, 2.5 mL Vial, Rx only, Compounded by Wise Pharmacy, Littleton, CO 80123.
D-1575-2019
Recall number D-1575-2019
Initiated July 22, 2019
Classification Class II
Status Terminated
Quantity 97 vials
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
Lack of Processing Controls
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Processing Controls
Code information Lot #: 5620N, Exp 7/16/2019; 6221N, Exp 8/31/2019; 6952N, Exp 10/16/2019
Distribution pattern CO, TX, WY
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[11597]
FDA event record
· Exact recall-number query on openFDA
drug · product 10 of 11
Papaverine/Phentolamine/Alprostadil 30 mg/2 mg/50 mcg/mL Injectable, 2.5 mL Vial, Rx only, Compounded by Wise Pharmacy, Littleton, CO 80123.
D-1576-2019
Recall number D-1576-2019
Initiated July 22, 2019
Classification Class II
Status Terminated
Quantity 32 vials
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
Lack of Processing Controls
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Processing Controls
Code information Lot #: 6176N, Exp 8/30/2019; 7162N, Exp 10/20/2019
Distribution pattern CO, TX, WY
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[11165]
FDA event record
· Exact recall-number query on openFDA
drug · product 11 of 11
Papaverine/Phentolamine/Alprostadil/Atropine 30 mg/2 mg/50 mcg/0.15 mg/mL Injectable, 2.5 mL Vial, Rx only, Compounded by Wise Pharmacy, Littleton, CO 80123.
D-1577-2019
Recall number D-1577-2019
Initiated July 22, 2019
Classification Class II
Status Terminated
Quantity 14 vials
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
Lack of Processing Controls
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of Processing Controls
Code information Lot #: 6153N, Exp8/29/2019
Distribution pattern CO, TX, WY
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[11609]
FDA event record
· Exact recall-number query on openFDA
