FDAFDA · Food and drugs·Recall number D-0729-2021
Acetaminophen 325 mg tablets, Regular Strength Pain Reliever, 100-count bottle, Distributed by: Walmart Inc., Bentoville, AR 72716, NDC 79903-052-10
Published August 25, 2021 · Recall initiated: June 16, 2021
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
cGMP deviations: Discolored acetaminophen
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Spirit Pharmaceuticals
- Distributor
- USA Nationwide
- Lot
- Lot #: S210240, Exp. 03/2023
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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