US Drug Recall Register
Class III · Low risk Terminated Initiated Apr 27, 2023 (3 years ago)

Fentanyl Buccal Tablets CII, 200mcg, packaged in cartons of 28 Buccal Tablets (4 tablets…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Labeling: Incorrect or Missing Package Insert

What was recalled

Fentanyl Buccal Tablets CII, 200mcg, packaged in cartons of 28 Buccal Tablets (4 tablets x 7 cards), Rx only, Distributed by: Mayne Pharma, Greenville, NC 27834, NDC 51862-635-28

Recalling firm
Teva Pharmaceuticals USA Inc
NDC code
51862-635-28
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0767-2023

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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