RecallRadar

FDA Drug recall D-1237-2020

Oxycodone and Acetaminophen Tablets, USP 10 mg*/325 mg 100-count bottles, Rx Only, Distributed by: Aurobindo Pharma USA, Inc

On 2020-04-22 the FDA classified a Class II recall of Oxycodone and Acetaminophen Tablets, USP 10 mg*/325 mg 100-count bottles, Rx Only, Distributed by: Aurobindo Pharma USA, Inc by Aurobindo Pharma Usa, citing CGMP Deviations: Products were manufactured in a processing area in which water leakage was observed.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1237-2020
ClassificationClass II
Statusterminated
Initiated2020-03-18
Published2020-04-22
Last updated2026-09-13 11:52 UTC
CompanyAurobindo Pharma Usa
DistributionUS

Product

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

Reason

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

Identifiers

ndc13107-043-30
ndc13107-043-01
ndc13107-043-05
ndc13107-043-99
ndc13107-044-30
ndc13107-044-01
ndc13107-044-05
ndc13107-044-99
ndc13107-045-30
ndc13107-045-01
ndc13107-045-05
ndc13107-045-99
ndc13107-046-30
ndc13107-046-01
ndc13107-046-05
ndc13107-046-99
code_infoLot #: 046180056A, Exp. Date 05/2020

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1237-2020%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.