Mckesson Medical-Surgical recalls Bupivacaine HCl injection vials due to temperature abuse risks. This may affect prescription products from Auromedics Pharma LLC. Consumers should check product details and contact the manufacturer for guidance.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical has recalled certain Bupivacaine HCl injection vials because they may have been exposed to improper temperatures during distribution. This could lead to unsafe drug conditions if the product is used without proper temperature control.
The recall is due to temperature abuse, meaning the product may have been stored or transported at temperatures that could compromise its safety. This could lead to improper drug conditions if not handled correctly.
Prescription drug users who received the recalled Bupivacaine HCl injection vials from Auromedics Pharma LLC. Healthcare professionals administering the drug are most at risk due to potential temperature-related safety issues.
Check for the product name 'Bupivacaine HCl Injection, Multi dose vial, 0.50%, 50 mL/5 mg/mL' with NDC 55150-0250-50. The recall affects prescription products distributed by Auromedics Pharma LLC.
Identify the product by checking the NDC number 55150-0250-50 and the specific product description.
The product was recalled due to temperature abuse during distribution, which could compromise its safety.
Check for the product name 'Bupivacaine HCl Injection, Multi dose vial, 0.50%, 50 mL/5 mg/mL' with NDC 55150-0250-50.
The recall does not specify a remedy, so contact Mckesson Medical-Surgical for guidance.
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-1001-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1001-2022 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
