FDARecall 99762Medicines
What to do
The FDA record of this recall has no instruction for consumers. Compare the lot codes below with your product. If they match, do not use it, and follow the notice of the firm or ask the store where you bought it. Talk to your pharmacist or doctor before stopping a medicine.Note from Recalls Watch, not agency text.
Read the official notice on accessdata.fda.gov (opens in a new tab)
Hazard
Why it was recalled
Defective Delivery System: Possibility of no medication in the prefilled pen.
FDA classification: Class II. Use may cause temporary or medically reversible health consequences, or the chance of serious consequences is remote. Status: Ongoing.
Is it yours? Products and codes
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
- Lot or code
- Lot #: AP250095A, Exp 2/28/2027
- FDA recall number
- D-0868-2026
- Quantity
- 5,694 pens
Distribution (FDA): USA Nationwide
About this record
- Issued by
- U.S. Food and Drug Administration
- Firm
- Amneal Pharmaceuticals of New York, LLC
- Title
- Composed by Recalls Watch from fields of the record; FDA records have no title.