Reported Mar 18, 2020 · Terminated
Acetaminophen 500 mg tablet packaged in a) 30-count bottles ( NDC 52959-0002-30), b) 42-count bottles (NDC…
H J Harkins Company Inc. dba Pharma Pac
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: H J Harkins Company Inc dba Pharma Pac · 1400 W Grand Ave Ste F · Grover Beach, CA · 93433-4221
Is this the product you have?
4 of 4 products
| # | Product as published |
|---|---|
| 1 | 30-count bottles ( NDC 52959-0002-30) |
| 2 | 42-count bottles (NDC 52959-0002-42) |
| 3 | 45-count bottles (NDC 52959-0002-45) and |
| 4 | 50-count bottles (NDC 52959-0002-50) Repack: H.J. Harkins Co., Inc. Grover Beach, CA 93433 |
- Lot codes and dates
Lot #: AE00Mexp. date 08/2021
- Amount recalled
- 11,973 tablets
Where it was sold
- Nationwide
Why it was recalled
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
This product could cause temporary or reversible health problems — stop using it.
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