RecallRadar

FDA Drug recall D-1408-2014

Dextroamphetamine Sulfate Tablets, USP, 10 mg, 100-count bottles, Rx only, Barr Laboratories, Inc., Pomona, NY 10970, NDC 0555-0953-02

On 2014-07-02 the FDA classified a Class II recall of Dextroamphetamine Sulfate Tablets, USP, 10 mg, 100-count bottles, Rx only, Barr Laboratories, Inc., Pomona, NY 10970, NDC 0555-0953-02 by Teva Pharmaceuticals Usa, citing failed Impurities/Degradation Specifications: this product is being recalled due to an out of specification test result for impurities during stability testing.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1408-2014
ClassificationClass II
Statusterminated
Initiated2014-05-01
Published2014-07-02
Last updated2026-09-13 11:51 UTC
CompanyTeva Pharmaceuticals Usa
DistributionUS

Product

Dextroamphetamine Sulfate Tablets, USP, 10 mg, 100-count bottles, Rx only, Barr Laboratories, Inc., Pomona, NY 10970, NDC 0555-0953-02.

Reason

Failed Impurities/Degradation Specifications: this product is being recalled due to an out of specification test result for impurities during stability testing.

Identifiers

ndc0555-0952-02
ndc0555-0953-02
code_infoLot # 34013122A, Exp 11/15

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1408-2014%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.