FDAClass IIJune 4, 2014

Cefpodoxime Proxetil Tablets recall

Cefpodoxime Proxetil Tablets, USP, 200 mg, 20 Tablet Bottles, Rx Only. Manufactured in Austria by Sandoz GmbH for Sandoz Inc. Princeton, NJ 08540. NDC…

Why was Cefpodoxime Proxetil Tablets recalled?

Presence of Foreign Substance: Presence of stainless steel particles.

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 #: DZ4056, Expiry: 11/2015; Lot # DZ4057, Expiry: 01/2016

Product
Cefpodoxime Proxetil Tablets, USP, 200 mg, 20 Tablet Bottles, Rx Only. Manufactured in Austria by Sandoz GmbH for Sandoz Inc. Princeton, NJ 08540. NDC…
Recalling firm
Sandoz, Inc
Quantity
22,818 Bottles
Distribution
Nationwide including Puerto Rico.
Recall date
June 4, 2014
Classification
Class II
Status
Terminated
Agency
FDA (drug)
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