PlainRecalls
FDA Drug Low Class III Terminated

Oxycodone and Acetaminophen Tablets, USP, 5 mg*/325 mg, 100-count bottle, Rx Only, Manufactured by: Mayne Pharma, Greenville, NC 27834, NDC 68308-841-01.

Reported: September 5, 2018 Initiated: August 21, 2018 #D-1129-2018

Product Description

Oxycodone and Acetaminophen Tablets, USP, 5 mg*/325 mg, 100-count bottle, Rx Only, Manufactured by: Mayne Pharma, Greenville, NC 27834, NDC 68308-841-01.

Reason for Recall

Labeling: Incorrect or Missing Lot and/or Exp Date: Lot FG10517 is mislabeled on the primary container with Lot FG01517, shipper labels and invoices contain the correct lot number of FG10517.

Details

Recalling Firm
Mayne Pharma Inc
Units Affected
6456 bottles
Distribution
Nationwide in the USA.
Location
Greenville, NC

Frequently Asked Questions

What product was recalled?
Oxycodone and Acetaminophen Tablets, USP, 5 mg*/325 mg, 100-count bottle, Rx Only, Manufactured by: Mayne Pharma, Greenville, NC 27834, NDC 68308-841-01.. Recalled by Mayne Pharma Inc. Units affected: 6456 bottles.
Why was this product recalled?
Labeling: Incorrect or Missing Lot and/or Exp Date: Lot FG10517 is mislabeled on the primary container with Lot FG01517, shipper labels and invoices contain the correct lot number of FG10517.
Which agency issued this recall?
This recall was issued by the FDA Drug on September 5, 2018. Severity: Low. Recall number: D-1129-2018.