Baxter recalls Doxil 50mg vials due to potential temperature exposure during shipping. Affected units may have been stored improperly, risking product instability.
CGMP Deviations: Product was exposed to temperatures exceeding the labeled storage conditions during transportation were released by mistake.
Baxter is recalling Doxil 50mg vials that may have been exposed to high temperatures during shipping. This could affect product stability and safety for patients using the medication.
The vials were exposed to temperatures above the labeled storage conditions during transportation. This could lead to product instability, though the risk of serious harm is not specified in the recall.
Patients prescribed Doxil by healthcare providers. Those using the recalled vials for cancer treatment are most at risk.
Check for the NDC code 0338-0067-01 and lot number MKZSU02 on the vial. The vial was manufactured for Baxter Healthcare Corporation in Deerfield, IL.
Look for NDC code 0338-0067-01 and lot number MKZSU02 on the vial label.
The recall states the vials may have been exposed to high temperatures during shipping, but does not specify if the product is unsafe for use.
Check for NDC code 0338-0067-01 and lot number MKZSU02 on the vial label.
The recall does not provide specific action steps for affected users.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall D-0048-2024 — Baxter Baxter Hello, I own a Baxter that is covered by recall D-0048-2024 from Baxter. 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.
