Acetaminophen & Codeine Phosphate Tablets recall: Labeling Error
Acetaminophen & Codeine Phosphate Tablets, 300 mg/30 mg, 15-count plastic bottle, Rx only, Mfr: Aurolife Pharma LLC, Dayton NJ, Packaged Exclusively…
Why was Acetaminophen & Codeine Phosphate Tablets recalled?
Labeling: Not elsewhere classified - count on the label was incorrect.
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 # 6050129, Exp 05/31/17
- Product
- Acetaminophen & Codeine Phosphate Tablets, 300 mg/30 mg, 15-count plastic bottle, Rx only, Mfr: Aurolife Pharma LLC, Dayton NJ, Packaged Exclusively…
- Recalling firm
- A-S Medication Solutions LLC.
- Quantity
- 2730 bottles
- Distribution
- Virginia
- Recall date
- May 11, 2016
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)