CareFusion 303, Inc. - 16344755
Due to affected devices that may have bent female IUI connector and may not be operable and potentially cause delays in the start of the infusion or monitoring.
CareFusion 303, Inc. - 16344755
This is a low risk product. CareFusion 303, Inc. is a company that produces medical devices and equipment. The product code 16344755 is a low risk product.
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Check for any signs of damage or malfunction in the device. Ensure that the device is used according to the manufacturer's instructions.
Check for any signs of damage or malfunction in the device.
Ensure that the device is used according to the manufacturer's instructions.
The product code for CareFusion 303, Inc. is 16344755.
Yes, this product is classified as low risk by CareFusion 303, Inc.
We’ve drafted a message you can send CareFusion 303, Inc. to request your refund or repair — edit it as you like.
Subject: Recall Z-3138-2024 — CareFusion 303, Inc. CareFusion 303, Inc. Hello, I own a CareFusion 303, Inc. that is covered by recall Z-3138-2024 from CareFusion 303, Inc.. 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.
