FDA recall record

Oxycodone and Acetaminophen Tablets, USP 10 mg*/325 mg 100-count bottles recall — FDA D-1237-2020

CGMP Deviations: Products were manufactured in a processing area in which water leakage was observed

Class IIclassification
D-1237-2020official record ID
Apr 22, 2020report date

Recall record at a glance

Official recordD-1237-2020
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmAurobindo Pharma USA Inc.
Report dateApr 22, 2020
Recall initiation dateMar 18, 2020
Quantity14707 units
LocationEast Windsor, NJ, United States

Official product description

Oxycodone and Acetaminophen Tablets, USP 10 mg*/325 mg 100-count bottles, Rx Only, Distributed by: Aurobindo Pharma USA, Inc. Dayton, NJ 08810, NDC 13107-046-01

Why the product was recalled

CGMP Deviations: Products were manufactured in a processing area in which water leakage was observed

Distribution information

Nationwide within the United States

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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