FDAClass IIAugust 30, 2023

All Over-The-Counter recall: CGMP Deviations

All Over-The-Counter (OTC) drug products warehoused, salvaged, and sold by Inmar.

Why was All Over-The-Counter recalled?

CGMP Deviations: Potential exposure to rodents and rodent activity in the distribution center. Also, due to unusually hot weather, FDA Recalled Products may have been subjected to temperatures in excess of storage condition instructions on product labeling.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA 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?

Miscellaneous

Product
All Over-The-Counter (OTC) drug products warehoused, salvaged, and sold by Inmar.
Recalling firm
Inmar Supply Chain Solutions, LLC
Quantity
Unknown
Distribution
Separate Distribution List (salvage buyers) provided by Inmar and will be uploaded. Final customer distribution unknown.
Recall date
August 30, 2023
Classification
Class II
Status
Ongoing
Agency
FDA (drug)
Open FDA enforcement record Latest recalls