Mckesson Medical-Surgical recalls Diprivan (Propofol) vials due to temperature abuse risks. This may cause product instability. Check your prescription vials for NDC 63323-269-29.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical is recalling Diprivan (Propofol) vials that may have been exposed to improper temperatures. This could cause the product to become unstable, potentially leading to unsafe use during medical procedures.
Temperature abuse means the vials were exposed to temperatures outside the safe range. This can cause the propofol to become unstable, which may lead to unsafe medical outcomes if used improperly.
Prescription patients receiving Diprivan (Propofol) vials with NDC 63323-269-29 are affected. Healthcare providers using these vials are at risk if they have improper temperature control.
Check your prescription vials for the NDC number 63323-269-29. The vials are labeled as Diprivan (Propofol) Emulsion, 200 mg per 20 mL (10mg/mL), 20 mL vials, and are for prescription use only.
Look for the NDC number 63323-269-29 on the vial label to confirm if it is recalled.
The recall is due to cGMP deviations related to temperature abuse, which could cause the product to become unstable.
Check the vial label for the NDC number 63323-269-29. The vials are labeled as Diprivan (Propofol) Emulsion, 200 mg per 20 mL (10mg/mL), 20 mL vials, and are for prescription use only.
The official recall notice does not specify a remedy or action for the recalled vials.
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-1116-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1116-2022 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.
