Mckesson recalls Ampicillin injections due to temperature abuse risks. Products distributed by Auromedics Pharma with NDC 55150-113-10 may be affected. Consumers should check product details and contact for guidance.
cGMP deviations: Temperature abuse
Mckesson is recalling Ampicillin injections that may have been exposed to improper temperatures. This could affect the medication's safety and effectiveness if not stored correctly.
Temperature abuse means the medication may have been stored or handled at unsafe temperatures, potentially compromising its safety and effectiveness. This could lead to ineffective treatment or adverse reactions if the product is used without proper temperature control.
Prescription holders of Ampicillin injections with NDC 55150-113-10. Healthcare providers and patients using the medication are most at risk if the product was stored incorrectly.
Check for the NDC code 55150-113-10 on the product label. The product is a 1 g per vial, 10-count box of Ampicillin for Injection, USP, distributed by Auromedics Pharma.
Look for the NDC code 55150-113-10 on the Ampicillin injection packaging.
The recall is due to cGMP deviations related to temperature abuse, which could affect the medication's safety and effectiveness.
Check for the NDC code 55150-113-10 on the Ampicillin injection packaging. The product is a 1 g per vial, 10-count box distributed by Auromedics Pharma.
The recall does not specify a remedy, so contact the manufacturer or your healthcare provider 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-1009-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1009-2022 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.
