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Class II: temporary or reversible health riskTerminated

GlaxoSmithKline Mupirocin Calcium Cream Recall

Mupirocin Calcium Cream, 2%, a) 15g tube (NDC 66993-942-15),b) 30g tube (NDC 66993-942-…

GlaxoSmithKline, LLC. · Zebulon, NC

Risk level
Class II
Reported by FDA
Sep 2, 2015
Recall ID
D-1362-2015
Check your lot numberHow we source this data

Summary

GlaxoSmithKline recalled Mupirocin Calcium Cream starting Aug 13, 2015. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1362-2015 on Sep 2, 2015. Reason: Penicillin Cross Contamination and Presence of Foreign Substance. Product was contaminated with penicillin and foreign substances during manufacturing process. Status: Terminated.

Why it was recalled

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

Product description

Mupirocin Calcium Cream, 2%, a) 15g tube (NDC 66993-942-15),b) 30g tube (NDC 66993-942-31), Rx only, Manufactured by Glaxo Operations UK Ltd, Harmire Road, Barnard Castle, UK for GlaxoSmithKline PO Box 1217 Zebulon, NC 27597-1217.

Lot numbers, UPCs & expiration codes

Lot #: C690076, C693373, Exp 2/2016; Lot #: C701378, C701376, Exp 4/2016; Lot #: C704164, Exp 5/2016; Lot #: C713687, Exp 8/2016; Lot #: C719467,C718203, Exp 9/2016; Lot #: C723641, Exp 10/2016; Lot #: C683884, Exp 12/2016; Lot #: C697653, Exp 3/2016; Lot #: C710477, Exp 7/2016; Expanded to include: C697654, Exp. 03/2016 (15 grams), C723642, Exp. 10/2016 (30 grams).

Where it was sold

Nationwide and Puerto Rico

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-1362-2015
Classification
Class II
Status
Terminated
Recall initiated
Aug 13, 2015
FDA report date
Sep 2, 2015
Quantity
166,070 of 15g tube, 112,720 of 30 g tube
Recall type
Voluntary: Firm initiated
Recalling firm
GlaxoSmithKline, LLC.

Original FDA data

Every field from FDA enforcement report D-1362-2015, exactly as published.

Show all FDA fields
City
Zebulon
State
NC
Status
Terminated
Country
United States
Event ID
71920
Address
1011 North Arendell Ave
Code information
Lot #: C690076, C693373, Exp 2/2016; Lot #: C701378, C701376, Exp 4/2016; Lot #: C704164, Exp 5/2016; Lot #: C713687, Exp 8/2016; Lot #: C719467,C718203, Exp 9/2016; Lot #: C723641, Exp 10/2016; Lot #: C683884, Exp 12/2016; Lot #: C697653, Exp 3/2016; Lot #: C710477, Exp 7/2016; Expanded to include: C697654, Exp. 03/2016 (15 grams), C723642, Exp. 10/2016 (30 grams).
Postal code
27597-1217
Report date
Sep 2, 2015
Product type
Drugs
Recall number
D-1362-2015
Classification
Class II
Recalling firm
GlaxoSmithKline, LLC.
Product quantity
166,070 of 15g tube, 112,720 of 30 g tube
Termination date
Mar 21, 2017
Reason for recall
Penicillin Cross Contamination and Presence of Foreign Substance. Product was contaminated with penicillin and foreign substances during manufacturing process.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Mupirocin Calcium Cream, 2%, a) 15g tube (NDC 66993-942-15),b) 30g tube (NDC 66993-942-31), Rx only, Manufactured by Glaxo Operations UK Ltd, Harmire Road, Barnard Castle, UK for GlaxoSmithKline PO Box 1217 Zebulon, NC 27597-1217.
Distribution pattern
Nationwide and Puerto Rico
Recall initiation date
Aug 13, 2015
Initial firm notification
Letter
Center classification date
Aug 25, 2015

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1362-2015, published Sep 2, 2015. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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