Acetaminophen and Codeine Phosphate Tablets recall: CGMP Deviations
Acetaminophen and Codeine Phosphate Tablets, USP, 300 mg/30 mg, 100-count bottles, Rx Only, Distributed by: Aurobindo Pharma USA, Inc., Dayton, NJ 08810, NDC 13107-059-99
Why was Acetaminophen and Codeine Phosphate Tablets recalled?
CGMP Deviations: Products were manufactured in a processing area in which water leakage was observed
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: 059180023A, 059180024A and 059180025A, Exp. Date 05/2021
- Product
- Acetaminophen and Codeine Phosphate Tablets, USP, 300 mg/30 mg, 100-count bottles, Rx Only, Distributed by: Aurobindo Pharma USA, Inc., Dayton, NJ 08810, NDC 13107-059-99
- Recalling firm
- Aurobindo Pharma USA Inc.
- Quantity
- 4332 units
- Distribution
- Nationwide within the United States
- Recall date
- April 22, 2020
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)