US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Jun 23, 2022 (4 years ago)

Refenesen Mucus Relief Tablet 30 Ct Sku 917531 Mucinex Dm Max…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

CGMP Deviations: product held outside appropriate storage temperature conditions.

What was recalled

REFENESEN MUCUS RELIEF TABLET 30 CT SKU 917531 MUCINEX DM MAX STRENGTH 7CT SKU 900854 RIC MUCUS RLF DM MAX STNGTH CHRY 6FL OZ SKU 999559 VICKS JARABE COUGH CONGESTION 8FLOZ SKU 998933 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.

Recalling firm
Family Dollar Stores, Llc.
Origin
VA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1456-2022

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.