RecallRadar

FDA Drug recall D-0414-2015

Ergoloid Mesylates ,1 mg tablets, 100 count bottle, Rx only, Manufactured by MUTUAL PHARMACEUTICAL CO., INC., PHILADELPHIA, PA 19124 USA fo…

On 2015-03-25 the FDA classified a Class II recall of Ergoloid Mesylates ,1 mg tablets, 100 count bottle, Rx only, Manufactured by MUTUAL PHARMACEUTICAL CO., INC., PHILADELPHIA, PA 19124 USA fo… by Mutual Pharmaceutical, citing failed Impurities/Degradation Specifications: during long-term stability testing.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0414-2015
ClassificationClass II
Statusterminated
Initiated2015-03-10
Published2015-03-25
Last updated2026-09-13 11:51 UTC
CompanyMutual Pharmaceutical
DistributionUS

Product

Ergoloid Mesylates ,1 mg tablets, 100 count bottle, Rx only, Manufactured by MUTUAL PHARMACEUTICAL CO., INC., PHILADELPHIA, PA 19124 USA for Sun Pharmaceutical Industries, Inc. 270 Prospect Plains Road, Cranbury, NJ 08512. NDC 53489-281-01

Reason

Failed Impurities/Degradation Specifications: during long-term stability testing.

Identifiers

code_infoLot #: 6557301, Exp 3/15; 6557401, Exp 3/15; 6557501, Exp 3/15; 6656301, Exp 10/16; 6687701, Exp 4/17.

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-0414-2015%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.