Mckesson Bupivacaine Injection Recall: Temperature Abuse Risk

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

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Mckesson Medical-Surgical recalls certain bupivacaine injections due to temperature abuse risks. This could lead to unsafe drug conditions if stored improperly. The recall does not include a specific remedy.

Why it’s dangerous

The recall mentions 'cGMP deviations: Temperature abuse', meaning the product may have been stored at unsafe temperatures. This could cause the drug to become unstable or ineffective, potentially leading to adverse effects.

Who’s affected

Prescribers and patients using the recalled bupivacaine injections. Those who received the product with NDC 55150-0170-30 are most at risk.

How to tell if you have this one

Check for the NDC code 55150-0170-30 on the vial label. The product is a single-dose bupivacaine injection (0.5%, 30 mL/5 mg/mL) for prescription use only.

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 55150-0170-30 on the vial label to confirm if it's affected.

✎ GovInfoNow

Questions people ask

Is there a remedy for this recall?

The recall record does not specify a remedy.

What is the specific product code for this recall?

The NDC code 55150-0170-30 is listed for the affected product.

How can I tell if I have the recalled product?

Check the vial label for the NDC code 55150-0170-30 and the product description: single-dose bupivacaine injection (0.5%, 30 mL/5 mg/mL).

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-0999-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical

Hello,

I own a Mckesson Medical-Surgical that is covered by recall D-0999-2022 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-0999-2022 (April 13, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0999-2022 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 Bupivacaine HCl Injection, single dose vial, 0.5%, 30 mL/5 mg/mL, Rx only, Manufacturer: Auromedics Pharma LLC, NDC

Recall notice