Mckesson Medical-Surgical recalls Propofol Injectable Emulsion vials due to temperature abuse risks. Affected products may have been shipped with improper temperature control.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical is recalling Propofol Injectable Emulsion vials because they may have been exposed to improper temperatures during shipping. This could lead to unsafe conditions for patients receiving the medication.
The recall is due to cGMP deviations related to temperature abuse. This means the vials may have been stored or transported at temperatures that could compromise their safety, potentially leading to unsafe medication conditions.
Healthcare providers who received the recalled vials from McKesson Medical-Surgical. Patients receiving Propofol injections are at risk if they use the recalled vials.
Check for Propofol Injectable Emulsion vials labeled 200 mg per 20 mL (10 mg per mL), twenty-five vials per package, manufactured by Teva Pharma USA. The product was distributed by McKesson Medical-Surgical with specific dates noted in the distribution records.
Identify if you have Propofol Injectable Emulsion vials with the specific labeling and manufacturing details mentioned in the recall notice.
The product was recalled due to cGMP deviations related to temperature abuse, which may have compromised its safety.
Check for Propofol Injectable Emulsion vials labeled 200 mg per 20 mL (10 mg per mL), twenty-five vials per package, manufactured by Teva Pharma USA.
The recall notice does not specify a remedy, so you should contact McKesson Medical-Surgical to determine next steps.
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-1078-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1078-2022 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.
