US Drug Recall Register
Class I · High risk Terminated Initiated Dec 7, 2020 (6 years ago)

TraZODONE Hydrochloride Tablets USP 100 mg, Rx Only, 1000-count Bottle, Manufactured for…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Product mix-up: Bottles of sildenafil and trazodone were inadvertently packaged together during bottling at a 3rd party facility.

What was recalled

TraZODONE Hydrochloride Tablets USP 100 mg, Rx Only, 1000-count Bottle, Manufactured for: AvKARE Pulaski, TN 38478, NDC 42291-834-10

Recalling firm
AVKARE Inc.
NDC code
42291-834-10
Origin
TN, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0168-2021

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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