HIGH
fentaNYL Citrate Injectable Solution in 0.9% Sodium Chloride, 50 mcg/5mL)(10 mcg per mL), wells pharma, NDC 73702-202-15.
Wells Pharma of Houston
cGMP deviations.
HIGH
fentaNYL Citrate Injectable Solution, NARCOTIC, Cii, 1000 mcg/100 mL (10 mcg per mL), 100 mL bag, Wells Pharma in Houston, NDC 73702-202-02.
Quick Facts at a Glance
- Recall Date
- April 1, 2026
- Hazard Level
- HIGH
- Brand
- Wells Pharma of Houston
- Geographic Scope
- 1 states
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- Wells Pharma of Houston
- Model numbers
- 120925202022769, Expiration Date 04/09/2026, 123125202022883, Expiration Date 05/05/2026, 123125202022884, Expiration Date 05/05/2026 011226202020057, Expiration Date 05/14/2026, 011226202020058 +8 more
- Where affected
- ALL
Hazard Information
cGMP deviations.
What You Should Do
Consumers and healthcare providers should stop using this product immediately. Contact Wells Pharma of Houston LLC or your healthcare provider for guidance. Notification method: Letter
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Full Description
fentaNYL Citrate Injectable Solution, NARCOTIC, Cii, 1000 mcg/100 mL (10 mcg per mL), 100 mL bag, Wells Pharma in Houston, NDC 73702-202-02.. Reason: cGMP deviations.. Classification: Class II. Quantity: 4,030 IV Bags. Distribution: U.S. Nationwide.
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Safety Guide
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Product Classification
Product Details
Model Numbers
120925202022769
Expiration Date 04/09/2026
123125202022883
Expiration Date 05/05/2026
123125202022884
+11 more
Affected States
ALL
Report Date
May 6, 2026
Source Agency
FDA - Drug SafetyRecall Status
ACTIVE
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