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Class II: temporary or reversible health riskTerminated

Allergan Sales Blephamide Recall

BLEPHAMIDE (sulfacetamide sodium and prednisolone acetate ophthalmic ointment, USP) 10 %/0

Allergan Sales, LLC · Waco, TX

Risk level
Class II
Reported by FDA
Sep 30, 2015
Recall ID
D-1820-2015
Check your lot numberHow we source this data

Summary

Allergan Sales recalled Blephamide starting Aug 24, 2015. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1820-2015 on Sep 30, 2015. Reason: Presence of Particulate Matter: Due to customer complaints of small black particles, identified as part of the ointment tube cap, generated by the action of unscrewing the cap from the aluminum tube and potentially introducing the particle into the product. Status: Terminated.

Why it was recalled

Presence of Particulate Matter: Due to customer complaints of small black particles, identified as part of the ointment tube cap, generated by the action of unscrewing the cap from the aluminum tube and potentially introducing the particle into the product.

Product description

BLEPHAMIDE (sulfacetamide sodium and prednisolone acetate ophthalmic ointment, USP) 10 %/0.2 %, 3.5 g tube, Rx only, ALLERGAN, Irvine, California 92612, NDC 0023-0313-04, UPC 3 00230 31304 9.

Lot numbers, UPCs & expiration codes

Lot #: 86430, Exp 09/17; 87806, Exp 02/18; 88147, Exp 03/18

Where it was sold

Nationwide, Puerto Rico, and Barbados

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-1820-2015
Classification
Class II
Status
Terminated
Recall initiated
Aug 24, 2015
FDA report date
Sep 30, 2015
Quantity
337 tubes
Recall type
Voluntary: Firm initiated
Recalling firm
Allergan Sales, LLC

Original FDA data

Every field from FDA enforcement report D-1820-2015, exactly as published.

Show all FDA fields
City
Waco
State
TX
Status
Terminated
Country
United States
Event ID
72016
Address
8301 Mars Dr
Code information
Lot #: 86430, Exp 09/17; 87806, Exp 02/18; 88147, Exp 03/18
Postal code
76712-6578
Report date
Sep 30, 2015
Product type
Drugs
Recall number
D-1820-2015
Classification
Class II
Recalling firm
Allergan Sales, LLC
Product quantity
337 tubes
Termination date
Apr 19, 2017
Reason for recall
Presence of Particulate Matter: Due to customer complaints of small black particles, identified as part of the ointment tube cap, generated by the action of unscrewing the cap from the aluminum tube and potentially introducing the particle into the product.
Voluntary / mandated
Voluntary: Firm initiated
Product description
BLEPHAMIDE (sulfacetamide sodium and prednisolone acetate ophthalmic ointment, USP) 10 %/0.2 %, 3.5 g tube, Rx only, ALLERGAN, Irvine, California 92612, NDC 0023-0313-04, UPC 3 00230 31304 9.
Distribution pattern
Nationwide, Puerto Rico, and Barbados
Recall initiation date
Aug 24, 2015
Center classification date
Sep 22, 2015

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1820-2015, published Sep 30, 2015. View the source record (openFDA) · FDA enforcement reports

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

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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