FDAClass IIAugust 18, 2021

Cimetidine Hydrochloride Oral Solution 300 mg/5 mL recall: CGMP Deviations

Cimetidine Hydrochloride Oral Solution 300 mg/5 mL, 8 fl oz (237 mL) Rx ONLY, Pharmaceutical Associates, Inc. Greenville, SC 29605, NDC 0121-0649-08

Why was Cimetidine Hydrochloride Oral Solution 300 mg/5 mL recalled?

Lack of CGMP: This recall is being carried out due to potential for carry over of Senna Syrup.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot: C62F Exp. 31OCT2022

Product
Cimetidine Hydrochloride Oral Solution 300 mg/5 mL, 8 fl oz (237 mL) Rx ONLY, Pharmaceutical Associates, Inc. Greenville, SC 29605, NDC 0121-0649-08
Recalling firm
PAI Holdings, LLC. dba Pharmaceutical Associates Inc
Quantity
400 cases (12 bottles/case)
Distribution
Distributed Nationwide in the USA
Recall date
August 18, 2021
Classification
Class II
Status
Terminated
Agency
FDA (drug)
Open FDA enforcement record Latest recalls