FDA recall record

Northwind Pharmaceuticals Prednisone 20 mg, Tablet, 10-count bottle recall — FDA D-0485-2016

Labeling: Not elsewhere classified. NDC number is incorrect on the container.

Class IIIclassification
D-0485-2016official record ID
Dec 9, 2015report date

Recall record at a glance

Official recordD-0485-2016
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmNorthwind Pharmaceuticals LLC
Report dateDec 9, 2015
Recall initiation dateNov 10, 2015
Quantity40 Bottles
LocationIndianapolis, IN, United States

Official product description

Prednisone 20 mg, Tablet, 10-count bottle, Rx only, Mfg by: HIKMA Pharmaceuticals PO BOX 182400 Amman 11118 Jordan. Dist By: West-Ward Pharmaceuticals Corp., Eatentown, NJ 07724 USA, Repackaged By: Northwind Pharmaceuticals, Indianapolis, IN 46256. NDC 51655-320-53

Why the product was recalled

Labeling: Not elsewhere classified. NDC number is incorrect on the container.

Distribution information

Nationwide

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: E-Mail.

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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