GlucaGen 1mg Injection Recall: Temperature Abuse Risk

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Contact the company & request your remedy

Recalling firmMckesson Medical-Surgical Inc. Corporate Office9954 Maryland Drive, Deep Run Iii Ste. 4000 · Richmond, VA 23233

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Mckesson Medical-Surgical is recalling GlucaGen 1mg glucagon injections because of temperature abuse risks. This could lead to unsafe product conditions if not stored properly.

Why it’s dangerous

The product was manufactured with cGMP deviations related to temperature abuse. This means the injections could be unsafe if stored or handled improperly.

Who’s affected

Prescription patients who received GlucaGen 1mg injections from Mckesson Medical-Surgical. Those with prescriptions distributed after the affected dates are most at risk.

How to tell if you have this one

Check your prescription label for the NDC 0597-0260-10. The recall affects products distributed after the specific dates mentioned in the distribution records.

Brand
Mckesson Medical-Surgical
Category
Drug

Based on the official FDA remedy

What to do — step by step

Check Prescription Dates
Review your prescription label for the distribution date to determine if it falls within the affected period.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The recall indicates potential temperature abuse risks, but the product is safe if stored and handled correctly.

How do I know if my product is affected?

Check your prescription label for NDC 0597-0260-10 and the distribution date mentioned in the recall notice.

What should I do if I have this product?

The recall does not specify a need to discard or return the product; check your prescription dates to see if it's affected.

Take action

Contact Mckesson Medical-Surgical

We’ve drafted a message you can send Mckesson Medical-Surgical to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall D-1017-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical

Hello,

I own a Mckesson Medical-Surgical that is covered by recall D-1017-2022 from Mckesson Medical-Surgical.

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.

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Where this comes from

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.

Official source: FDA Recall #D-1017-2022 (April 13, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1017-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Mckesson Medical-Surgical Inc. Corporate Office recalls GlucaGen (glucagon) for injection, 1 mg per vial, single dose kit, Rx only, Manufactured for: Boehringer Mannheim, NDC

Lower-risk recall