RecallDepth
Class II Terminated

Methylphenidate Hydrochloride Extended-Release Capsules (LA), 20 mg, 100 count bottle, Rx only, TEVA PHARMACEUTICALS USA, NDC 0093-5346-01

Company
Teva Pharmaceuticals Usa, Inc.
Recall Initiated
June 18, 2013
Posted
August 14, 2013
Recall Number
D-847-2013
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
16,293 bottles
Firm Location
Sellersville, PA, United States

Reason for Recall

Failed Dissolution Specifications: Product is being recalled due to out of specification dissolution results obtained during routine stability testing.

Distribution

Nationwide

Lot / Code Info

34010282A, 34010283A, 34010284A, 34010285A, 34010286A and 34010565A, exp 04/14; 34013199A, 34013200A, 34013201A, 34013202A and 34013203A, exp 10/14.

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