FDA recall record

GlaxoSmithKline, LLC Bactroban Ointment (mupirocin calcium), 2% 22g tube ,Rx only recall — FDA D-1360-2015

Penicillin Cross Contamination and Presence of Foreign Substance. Product was contaminated with penicillin and foreign substances during manufacturing…

Class IIclassification
D-1360-2015official record ID
Sep 2, 2015report date

Recall record at a glance

Official recordD-1360-2015
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmGlaxoSmithKline, LLC.
Report dateSep 2, 2015
Recall initiation dateAug 13, 2015
Quantity19,520 tubes
LocationZebulon, NC, United States

Official product description

Bactroban Ointment (mupirocin calcium), 2% 22g tube ,Rx only, Manufactured by Glaxo Operations UK Ltd, Harmire Road, Barnard Castle, UK for GlaxoSmithKline PO Box 1217 Zebulon, NC 27597-1217. NDC 0029-1525-44

Why the product was recalled

Penicillin Cross Contamination and Presence of Foreign Substance. Product was contaminated with penicillin and foreign substances during manufacturing process.

Distribution information

Nationwide and Puerto Rico

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA 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

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