RecallRadar

FDA Drug recall D-0723-2026

Glucagon Emergency Kit for Low Blood Sugar, Glucagon for Injection USP, 1mg per vial, Diluent for Glucagon, 1 mL syringe, Rx only, Manufact…

On 2026-07-08 the FDA classified a Class II recall of Glucagon Emergency Kit for Low Blood Sugar, Glucagon for Injection USP, 1mg per vial, Diluent for Glucagon, 1 mL syringe, Rx only, Manufact… by Lupin Pharmaceuticals, citing CGMP deviation: OOS result observed for the Gliding Force functionality test during 12-month long term stability testing.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0723-2026
ClassificationClass II
Statusongoing
Initiated2026-06-23
Published2026-07-08
Last updated2026-09-13 11:52 UTC
CompanyLupin Pharmaceuticals
DistributionUS

Product

Glucagon Emergency Kit for Low Blood Sugar, Glucagon for Injection USP, 1mg per vial, Diluent for Glucagon, 1 mL syringe, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Naples, FL 34108, Manufactured by: Lupin Limited, Nagpur - 441108, INDIA, NDC 70748-311-01

Reason

CGMP deviation: OOS result observed for the Gliding Force functionality test during 12-month long term stability testing.

Identifiers

ndc70748-311-01
ndc70748-309-01
ndc70748-310-01
code_info
Kit Lots: WB00010, Exp. Date Jan 2027; WB00017, WB00019, Exp. Date Feb 2027; WB00070, Exp. Date Jun 2027; WB00077, WB00…Kit Lots: WB00010, Exp. Date Jan 2027; WB00017, WB00019, Exp. Date Feb 2027; WB00070, Exp. Date Jun 2027; WB00077, WB00078, Exp. Date Jul 2027; WB00130, Exp. Date Nov 2027.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0723-2026%22

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