PlainRecalls
FDA Drug Moderate Class II Ongoing

Safe tussin PM, NIGHT TIME Cough Relief, (Dextromethorphan HBr, USP 7.5mg, Doxylamine Succinate 3.125mg), 4.0 FL OZ (118mL) bottle, Kramer Laboratories , Inc. Bridgewater, NJ 08807.

Reported: June 7, 2023 Initiated: May 3, 2023 #D-0775-2023

Product Description

Safe tussin PM, NIGHT TIME Cough Relief, (Dextromethorphan HBr, USP 7.5mg, Doxylamine Succinate 3.125mg), 4.0 FL OZ (118mL) bottle, Kramer Laboratories , Inc. Bridgewater, NJ 08807.

Reason for Recall

CGMP Deviations: Use of non-food grade lubricant in mixing vessel.

Details

Units Affected
13,968 bottles
Distribution
Product was distributed Nationwide.
Location
Lincoln, RI

Frequently Asked Questions

What product was recalled?
Safe tussin PM, NIGHT TIME Cough Relief, (Dextromethorphan HBr, USP 7.5mg, Doxylamine Succinate 3.125mg), 4.0 FL OZ (118mL) bottle, Kramer Laboratories , Inc. Bridgewater, NJ 08807.. Recalled by Denison Pharmaceuticals, LLC. Units affected: 13,968 bottles.
Why was this product recalled?
CGMP Deviations: Use of non-food grade lubricant in mixing vessel.
Which agency issued this recall?
This recall was issued by the FDA Drug on June 7, 2023. Severity: Moderate. Recall number: D-0775-2023.