FDAFDA · Food and drugs·Recall number D-1005-2020
Acetaminophen 500 mg tablet packaged in a) 30-count bottles ( NDC 52959-0002-30), b) 42-count bottles (NDC 52959-0002-42), c) 45-count bottles (NDC 52959-0002-45) and e) 50-count bottles (NDC 52959-0002-50) Repack: H.J. Harkins Co., Inc. Grover Beach, CA 93433
Published March 18, 2020 · Recall initiated: March 6, 2020
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
Presence of Foreign Tablets/Capsules: Complaint involving one Women's Prenatal dietary supplement tablet commingled in a bottle of Extra Strength Acetaminophen 500 mg contents 1000 count bottle
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- H J Harkins Company Inc dba Pharma Pac
- Distributor
- Nationwide within the United States
- Lot
- Lot #: AE00M, exp. date 08/2021
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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