RecallRadar

FDA Drug recall D-1405-2015

ALLOPURINOL TABLETS, USP, 300 mg, 500 count bottle, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811 --- NDC 0603…

On 2015-09-09 the FDA classified a Class III recall of ALLOPURINOL TABLETS, USP, 300 mg, 500 count bottle, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811 --- NDC 0603… by Qualitest Pharmaceuticals, citing failed Tablet/Capsule Specifications; report of oversized and discolored tablets.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1405-2015
ClassificationClass III
Statusterminated
Initiated2015-07-20
Published2015-09-09
Last updated2026-09-13 11:51 UTC
CompanyQualitest Pharmaceuticals
DistributionUS

Product

ALLOPURINOL TABLETS, USP, 300 mg, 500 count bottle, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811 --- NDC 0603-2116-28

Reason

Failed Tablet/Capsule Specifications; report of oversized and discolored tablets

Identifiers

ndc0603-2115-93
ndc0603-2115-21
ndc0603-2115-28
ndc0603-2115-32
ndc0603-2115-02
ndc0603-2115-04
ndc0603-2116-02
ndc0603-2116-21
ndc0603-2116-28
ndc0603-2116-32
code_infoCP0761501, Exp. 12/16

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-1405-2015%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.