Proair Inhaler Recall: Temperature Abuse Risk

Take action

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 Proair inhalers that may have been exposed to improper temperatures during shipping. This could affect the medication's safety and effectiveness.

Why it’s dangerous

Temperature abuse during shipping can cause the inhaler to become unstable. This may lead to inconsistent medication delivery or safety issues if the product is used improperly.

Who’s affected

Prescription inhaler users who received Proair from Mckesson Medical-Surgical. Those with specific lot numbers or shipping dates may be affected.

How to tell if you have this one

Check for the product name 'Proair HFA (albuterol sulfate) Inhalation Aerosol' with NDC 59310-579-22. Products were distributed by Mckesson Medical-Surgical between the dates listed in the recall notice.

Brand
Mckesson Medical-Surgical
Category
Drug

Based on the official FDA remedy

What to do — step by step

Check Product Details
Review the product label for the NDC number 59310-579-22 and the distribution dates provided in the recall notice.

✎ GovInfoNow

Questions people ask

Why is this inhaler being recalled?

The recall is due to potential temperature abuse during shipping, which could affect the medication's safety and effectiveness.

How can I tell if I have the recalled product?

Check for the NDC number 59310-579-22 on the product label and verify the distribution dates listed in the recall notice.

What should I do if I have the recalled product?

The recall notice does not specify a specific action for affected products. Check the product details and contact your pharmacy for further 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-1076-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical

Hello,

I own a Mckesson Medical-Surgical that is covered by recall D-1076-2022 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.

Similar recalls

From people who’ve dealt with this

Experiences, tips, and questions from readers. Every comment is reviewed before it appears.

No comments yet — be the first to share your experience.

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-1076-2022 (April 13, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1076-2022 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 Proair, HFA (albuterol sulfate) Inhalation Aerosol 90 mcg per actuation, 200 metered inhalations, Rx only, MFG: Teva

Lower-risk recall