RecallRadar

FDA Drug recall D-1424-2015

Imipramine HCl Tablets, USP, 25 mg, 100 count bottles, Mfd By: Mutual Pharmaceutical Co., Inc., Philadelphia, PA --- NDC 54738-913-01

On 2015-09-16 the FDA classified a Class III recall of Imipramine HCl Tablets, USP, 25 mg, 100 count bottles, Mfd By: Mutual Pharmaceutical Co., Inc., Philadelphia, PA --- NDC 54738-913-01 by Mutual Pharmaceutical, citing chemical Contamination; benzophenone leached from the product label varnish.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1424-2015
ClassificationClass III
Statusterminated
Initiated2015-07-16
Published2015-09-16
Last updated2026-09-13 11:51 UTC
CompanyMutual Pharmaceutical
DistributionUS

Product

Imipramine HCl Tablets, USP, 25 mg, 100 count bottles, Mfd By: Mutual Pharmaceutical Co., Inc., Philadelphia, PA --- NDC 54738-913-01

Reason

Chemical Contamination; benzophenone leached from the product label varnish

Identifiers

code_infolot #s: 6655001, exp 8/16, 6679801, exp 2/17, 6690302, exp 4/17 and 6706001, exp 7/17

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-1424-2015%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.