D-1056-2017 Class II Terminated

Recalled by Teva Pharmaceuticals USA — North Wales, PA

Recall Details

Product Type
Drugs
Report Date
August 9, 2017
Initiation Date
July 24, 2017
Termination Date
January 31, 2018
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
28,188 bottles

Product Description

Famotidine Tablets USP, 20 mg, 100 count bottles, Rx only, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA --- NDC 0172-5728-60

Reason for Recall

Failed Tablet/Capsule Specification; out of specification for tablet weight

Distribution Pattern

Nationwide

Code Information

Lot # 3429066, exp 06/2018