Amneal Pharmaceuticals of New York, LLC — Exenatide Injection, USP, 250 mcg/mL, 1.2 mL per prefilled pen, Rx Only, Subcutaneous Use Only, For Single Patient Use Only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Ahme
Official product recall notices and clearly labeled enforcement reference records.
Reference record — not a live warning · enforcement-reference · official-source
Defective Delivery System: Possibility of no medication in the prefilled pen.
- Provider
- FDA — drug enforcement reference
- Source observed
- 9/30/2026, 12:00:00 AM UTC
- Source updated
- 9/30/2026, 12:00:00 AM UTC
- Location
- Brookhaven, NY, US
- hazard
- Defective Delivery System: Possibility of no medication in the prefilled pen.
- notice
- Periodic enforcement reference; not a real-time safety alert or a reliable recall-lifecycle tracker.
- product
- Exenatide Injection, USP, 250 mcg/mL, 1.2 mL per prefilled pen, Rx Only, Subcutaneous Use Only, For Single Patient Use Only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Ahmedabad 382213, India; Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807, NDC 70121-1685-1
- distribution
- USA Nationwide
- manufacturer
- Amneal Pharmaceuticals of New York, LLC
- recall number
- D-0868-2026
- source status
- Ongoing
- classification
- Class II
- freshness minutes
- 180
Source use policy · openFDA reference data; not a real-time public alert service
Update history (1 recent revisions)
- 10/8/2026, 1:40:26 AM UTC
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