Mckesson recalls certain bupivacaine injections due to temperature abuse risks. This may affect prescription-only products from Auromedics. No specific remedy is listed in the recall notice.
cGMP deviations: Temperature abuse
Mckesson is recalling bupivacaine injections that may have been exposed to improper temperatures. This could lead to unsafe drug conditions if the product was not stored correctly. Patients should not use these products without consulting their healthcare provider.
The recall is due to cGMP deviations related to temperature abuse. This means the product may have been stored or handled at unsafe temperatures, potentially causing the injection to become unstable or ineffective.
Prescription patients who received bupivacaine injections from this recall. Healthcare providers using these products are at risk if they have improper temperature control.
Check for the product name 'Bupivacaine HCl Injection, single dose vial, Preservative Free 0.5%, 10mL (25/ct)' from Auromedics. The recall covers prescription-only products distributed by Mckesson Medical-Surgical.
Verify the product name and manufacturer on the vial label to confirm if it matches the recalled items.
The recall is due to cGMP deviations related to temperature abuse, meaning the product may have been stored or handled at unsafe temperatures.
The recall notice does not specify any remedy or action steps for consumers.
Check for the product name 'Bupivacaine HCl Injection, single dose vial, Preservative Free 0.5%, 10mL (25/ct)' from Auromedics. The recall covers prescription-only products distributed by 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.
Subject: Recall D-0998-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-0998-2022 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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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.
