Mckesson Medical-Surgical recalls Cefaz: Cefazolin for injection and Dextrose injections due to temperature abuse during storage, posing risks of ineffective treatment. Affected products were distributed with specific dates.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical recalls Cefazolin injections and Dextrose solutions because they may have been exposed to improper temperatures, potentially leading to ineffective treatment. This recall affects prescription products distributed with specific dates.
The products may have been exposed to temperatures outside the recommended range during storage, which can cause the medication to become ineffective. This temperature abuse could lead to treatment failures if the medication is not properly stored.
Prescription patients who received Cefazolin or Dextrose injections from Mckesson Medical-Surgical. Healthcare providers using these products are most at risk due to potential temperature issues.
Check for Cefazolin for injection USP and Dextrose Injection USP, 2 g, 50 mL duplex container, Rx only, manufactured by B. Braun Medical. Products were distributed with specific dates that impacted the customer.
Identify the product by checking the NDC number 0264-3105-11 and the distribution dates mentioned in the recall notice.
The recall is due to temperature abuse during storage, which may cause the medication to become ineffective.
Check for Cefazolin for injection USP and Dextrose Injection USP, 2 g, 50 mL duplex container, Rx only, manufactured by B. Braun Medical with specific distribution dates.
The recall notice does not specify a remedy, so contact Mckesson Medical-Surgical 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-1118-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1118-2022 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.
