PlainRecalls
FDA Drug Moderate Class II Terminated

Acetaminophen 325 mg tablets, Regular Strength Pain Reliever, 100-count bottle, Distributed by: Walmart Inc., Bentoville, AR 72716, NDC 79903-052-10

Reported: August 25, 2021 Initiated: June 16, 2021 #D-0729-2021

Product Description

Acetaminophen 325 mg tablets, Regular Strength Pain Reliever, 100-count bottle, Distributed by: Walmart Inc., Bentoville, AR 72716, NDC 79903-052-10

Reason for Recall

cGMP deviations: Discolored acetaminophen

Details

Recalling Firm
Spirit Pharmaceuticals
Units Affected
N/A
Distribution
USA Nationwide
Location
Ronkonkoma, NY

Frequently Asked Questions

What product was recalled?
Acetaminophen 325 mg tablets, Regular Strength Pain Reliever, 100-count bottle, Distributed by: Walmart Inc., Bentoville, AR 72716, NDC 79903-052-10. Recalled by Spirit Pharmaceuticals. Units affected: N/A.
Why was this product recalled?
cGMP deviations: Discolored acetaminophen
Which agency issued this recall?
This recall was issued by the FDA Drug on August 25, 2021. Severity: Moderate. Recall number: D-0729-2021.