Mckesson Medical-Surgical recalls Intralipid 20% IV fat emulsion bags (250mL) due to temperature abuse. This may cause product instability. Patients and healthcare providers should check product details and contact the manufacturer for guidance.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical is recalling Intralipid 20% IV fat emulsion bags (250mL) because of temperature abuse issues. This could lead to product instability, which might affect patient safety during medical treatments.
Temperature abuse can cause the product to become unstable. This instability may lead to potential issues during medical administration, such as incorrect dosing or adverse reactions.
Healthcare providers and patients who have received this specific Intralipid product for medical use. Those using the product without proper temperature control are at higher risk.
Check for Intralipid 20% IV fat emulsion bags (250mL) with NDC 0338-0519-09. The product is prescription-only and manufactured by Baxter Healthcare. McKesson Medical-Surgical cannot identify specific lot numbers for affected customers.
Verify the product name, size, and NDC number to confirm if it matches the recalled Intralipid 20% IV fat emulsion (250mL) with NDC 0338-0519-09.
The product was recalled due to temperature abuse, which can cause instability and potential safety issues during medical use.
Check for Intralipid 20% IV fat emulsion bags (250mL) with NDC 0338-0519-09. McKesson Medical-Surgical cannot identify specific lot numbers for affected customers.
Contact McKesson Medical-Surgical for guidance on next steps. The recall does not specify a specific action for consumers.
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-1119-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1119-2022 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
