Mckesson Medical-Surgical recalls Propofol Injectable Emulsion due to temperature abuse risks. This product is for medical use only and may be unsafe if exposed to improper temperatures.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical has recalled specific Propofol Injectable Emulsion products due to temperature abuse risks. This could lead to unsafe conditions if the product is exposed to improper temperatures during storage or use.
The recall is due to cGMP deviations related to temperature abuse. This means the product may be unsafe if it is exposed to temperatures that could affect its stability or safety.
Healthcare professionals and patients who have received the recalled Propofol products. Those using the product in medical settings are most at risk.
Check for Propofol Injectable Emulsion, USP, 200 mg/20 mL (10 mg/mL) in 50 mL vials (packs of 20, NDC 00591-2136-51) or 100 mL vials (packs of 10, NDC 00591-2136-68). The product is prescription-only and distributed by Teva Pharma USA.
Identify the product by checking the NDC codes: 00591-2136-51 for 50 mL vials or 00591-2136-68 for 100 mL vials.
The product is recalled due to temperature abuse risks, so it is not safe to use as intended without proper temperature control.
The official recall notice does not specify a remedy, so contact your healthcare provider or the manufacturer for guidance.
Check for Propofol Injectable Emulsion, USP, 200 mg/20 mL (10 mg/mL) in 50 mL vials (packs of 20, NDC 00591-2136-51) or 100 mL vials (packs of 10, NDC 00591-2136-68).
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-1077-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1077-2022 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.
