PlainRecalls
FDA Drug Moderate Class II Terminated

Maximum Strength Acid Reducer, Ranitidine tablets, USP 150 mg, 8 tablets. [NDC: Brand] NDC Good Sense:0113-0852-51; NDC Walgreens 0363-0852-51

Reported: March 25, 2020 Initiated: October 23, 2019 #D-1017-2020

Product Description

Maximum Strength Acid Reducer, Ranitidine tablets, USP 150 mg, 8 tablets. [NDC: Brand] NDC Good Sense:0113-0852-51; NDC Walgreens 0363-0852-51

Reason for Recall

CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

Details

Recalling Firm
Perrigo Company PLC
Distribution
Nationwide USA
Location
Allegan, MI

Frequently Asked Questions

What product was recalled?
Maximum Strength Acid Reducer, Ranitidine tablets, USP 150 mg, 8 tablets. [NDC: Brand] NDC Good Sense:0113-0852-51; NDC Walgreens 0363-0852-51. Recalled by Perrigo Company PLC.
Why was this product recalled?
CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Which agency issued this recall?
This recall was issued by the FDA Drug on March 25, 2020. Severity: Moderate. Recall number: D-1017-2020.