Class II · Moderate risk
Glucagon Emergency Kit for Low Blood Sugar
CGMP deviation: OOS result observed for the Gliding Force functionality test during 12-month long term stability testing.
Is Glucagon recalled?
Yes — there is an active recall. 1 ongoing FDA recall mention Glucagon (6 total). Check the affected lots below.
Most common reason: Temperature excursion (3 of these recalls)
Recalls are matched by product description. A recall usually affects specific lots, not every package of Glucagon. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Glucagon recalls in 2026
1 initiated in 2026, 6 in total — newest first
Class II · Moderate risk
Glucagon Emergency Kit for Low Blood Sugar
cGMP deviations: Temperature abuse
Class II · Moderate risk
Glucagen (glucagon)
cGMP deviations: Temperature abuse
Class II · Moderate risk
GlucaGen (glucagon)
cGMP deviations: Temperature abuse
Class I · High risk
Glucagon Emergency Kit for Low Blood Sugar
SUBPOTENT DRUG: Vial contained a liquid substance, instead of the expected powder substance. There was also a lack of full drug effect upon administration.
Class I · High risk
GlucaGen HypoKit
Defective delivery system: detached needles on the syringe in the kit.
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