Mckesson Albuterol Inhaler 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 is recalling albuterol inhalers that may have been affected by temperature abuse during shipping. This could lead to unsafe product conditions, but the recall does not specify a direct risk of injury.

Why it’s dangerous

The recall mentions 'cGMP deviations: Temperature abuse,' meaning the product may have been exposed to temperatures that could affect its safety during shipping. However, the specific hazard mechanism is not detailed in the record.

Who’s affected

Prescription holders of albuterol inhalers with NDC 0781-7296-85 are affected. Those who received the product through McKesson Medical-Surgical are most at risk.

How to tell if you have this one

Check your albuterol inhaler label for NDC 0781-7296-85. Products distributed by Sandoz Inc. are part of this recall. The recall covers prescription-only inhalers with a dose indicator.

Brand
Mckesson Medical-Surgical
Category
Drug

Based on the official FDA remedy

What to do — step by step

Check Product Label
Look for the NDC code 0781-7296-85 on your albuterol inhaler.

✎ GovInfoNow

Questions people ask

Is this inhaler dangerous?

The recall states there may be temperature abuse issues, but it does not specify a direct risk of injury.

How do I know if I have the recalled product?

Check your inhaler label for NDC 0781-7296-85. Products distributed by Sandoz Inc. are part of this recall.

What should I do if I have this product?

The recall does not specify a remedy, so contact your healthcare provider for guidance.

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-1024-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical

Hello,

I own a Mckesson Medical-Surgical that is covered by recall D-1024-2022 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-1024-2022 (April 13, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1024-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 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 Albuterol Sulfate Inhalation Aerosol HFA 90 mcg, with Dose Indicator, 200 metered inhalations, Rx only, Distributed by:

Recall notice