Mckesson Medical-Surgical recalls Cefazolin and Dextrose injections due to temperature abuse risks. Products may have been shipped without proper temperature control, potentially causing safety issues.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical is recalling Cefazolin for injection and Dextrose injection products because they may have been exposed to improper temperatures during shipping. This could lead to unsafe conditions for patients using these medications.
The products may have been shipped without proper temperature control, which can cause the medication to become unsafe for use. Temperature abuse risks could lead to ineffective treatment or adverse reactions if the medication is not stored or handled correctly.
Healthcare providers and patients who received these injections from pharmacies or hospitals that used the recalled products. Those who have the specific product with the NDC number 0264-3103-11 are most at risk.
Check for the product name and NDC number 0264-3103-11 on the packaging. The products are for prescription use only and were distributed by Mckesson Medical-Surgical.
Look for the NDC number 0264-3103-11 on the packaging to identify if the product is recalled.
The products may have been shipped without proper temperature control, which can cause the medication to become unsafe for use.
Check for the NDC number 0264-3103-11 on the packaging. The products are for prescription use only and were distributed by Mckesson Medical-Surgical.
Check the product details to see if it matches the NDC number 0264-3103-11. If it does, contact your pharmacy or healthcare provider for further instructions.
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-1117-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1117-2022 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.
