FDA recall record

Mayne Pharma Oxycodone and Acetaminophen Tablets, USP, 5 mg*/325 mg, 100-count bottle recall — FDA D-1129-2018

Labeling: Incorrect or Missing Lot and/or Exp Date: Lot FG10517 is mislabeled on the primary container with Lot FG01517, shipper labels and invoices…

Class IIIclassification
D-1129-2018official record ID
Sep 5, 2018report date

Recall record at a glance

Official recordD-1129-2018
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmMayne Pharma Inc.
Report dateSep 5, 2018
Recall initiation dateAug 21, 2018
Quantity6456 bottles
LocationGreenville, NC, United States

Official 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.

Why the product was 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.

Distribution information

Nationwide in the USA.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement 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

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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