RecallDepth
Class II Terminated

Blephamide (sulfacetamide sodium and prednisolone acetate ophthalmic ointment, USP) 10%/0.2% sterile, 3.5 g tube, RX only, Manufactured by Allergan, Irvine, California, 92612, U.S.A., NDC: 0023-0313-04.

Company
Allergan Sales, Llc
Recall Initiated
May 1, 2017
Posted
July 5, 2017
Recall Number
D-0929-2017
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
648 units
Firm Location
Waco, TX, United States

Reason for Recall

Failed Impurities/Degradation Specifications: stability testing results did not meet the specification for impurities.

Distribution

Nationwide in the US

Lot / Code Info

Lot: 93802, EXP NOV 2019

More recalls by Allergan Sales, Llc

View all recalls by this company →

Other recent Class II Drug recalls