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Glucagon Emergency Kit
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DRUG RECALLMODERATE

Glucagon Emergency Kit

Lupin recalls Glucagon Emergency Kits due to a stability test failure that may impair emergency use.

What to do

Check your kit's NDC 70748-311-01. If affected, stop using the kit and contact Lupin Pharmaceuticals for a replacement or refund.

Recalled
Listed
Updated
Recall No.
N/A
Agency
FDA
Firm
Lupin Pharmaceuticals Inc.
Recall ID
99296
Status
ONGOING

Recall at a glance

Quantity recalled
64,894 units

Why it was recalled

Lupin Pharmaceuticals is recalling Glucagon Emergency Kits (Glucagon for Injection USP, 1 mg per vial, with diluent and syringe) due to a CGMP deviation: an out-of-specification result was observed for the gliding force functionality test during 12-month long-term stability testing, which may affect the device's performance during an emergency.

Is mine affected?

Check the NDC or UPC and strength printed on the package. Yours is affected if it matches one below.

Glucagon Emergency Kit for Low Blood Sugar, Glucagon for Injection USPLot code: WB00010, 2027Strength: 1 mgNDC / UPC: NDC 70748-311-01

Recall #
N/A
D-0723-2026

Where it was sold

Distributed nationwide.

Timeline

  1. Firm initiated recall
  2. Publicly announced
  3. Listed on Recall Canary
  4. Summary updated

Official source

View on U.S. Food and Drug Administration →

Other Failed Specifications recalls

Other recent recalls from Lupin Pharmaceuticals Inc.

All recalls from Lupin Pharmaceuticals Inc.

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Editorial summary by Recall Canary · summary updated 2026-07-24 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification