Lupin Pharmaceuticals recalls Glucagon Emergency Kits due to a CGMP deviation in stability testing. Affected kits have specific lot numbers and expiration dates. Consumers should contact the manufacturer for details.
CGMP deviation: OOS result observed for the Gliding Force functionality test during 12-month long term stability testing.
Lupin Pharmaceuticals is recalling Glucagon Emergency Kits for low blood sugar treatment due to a manufacturing issue found during stability testing. This could affect the kit's reliability in emergencies, so affected users should check their lot numbers and contact Lupin for guidance.
The recall is for a CGMP deviation observed during long-term stability testing. This means the kit may not function properly under normal storage conditions, potentially affecting its emergency use.
People with diabetes who use Glucagon Emergency Kits are likely affected. Those with kits containing specific lot numbers and expiration dates listed in the recall are at risk.
Check the kit's lot number on the packaging. Affected lots include WB00010 (exp. Jan 2027), WB00017, WB00019 (exp. Feb 2027), WB00070 (exp. Jun 2027), WB00077, WB00078 (exp. Jul 2027), and WB00130 (exp. Nov 2027).
Look for the lot number on the packaging to determine if it is one of the affected lots listed in the recall.
The recall is due to a CGMP deviation observed during long-term stability testing, which may affect the kit's reliability in emergencies.
Check the lot number on your kit. If it matches the affected lots listed, contact Lupin Pharmaceuticals for further instructions.
The recall indicates a potential reliability issue, but no specific injury risk is mentioned in the official notice.
We’ve drafted a message you can send Lupin to request your refund or repair — edit it as you like.
Subject: Recall D-0723-2026 — Lupin Lupin Hello, I own a Lupin that is covered by recall D-0723-2026 from Lupin. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
