Carefusion recalls titanium bipolar forceps due to missing power supply and cleaning instructions in user manual. Affected models include F-5006 with UDI 10885403041006. Consumers should contact Carefusion for details.
BD has determined that the Instructions For Use (IFU) provided by BD is missing certain content that is contained in the manufacturer's IFU. This missing content is related to the interface with the device power supply, as well as cleaning and maintenance instructions. Refer to the attached V. Mueller" Bipolar Forcep IFU.
Carefusion is recalling titanium bipolar forceps that have missing power supply and cleaning instructions in their user manual. This could lead to improper use or damage if the user follows outdated instructions.
The user manual lacks critical instructions for connecting the device to power and cleaning the tools. Without these, medical staff might use the forceps incorrectly, potentially causing damage or injury.
Medical professionals using these forceps for surgery or procedures are most at risk. The recall affects specific models sold with UDI 108:885403041006.
Check for the model number F-5006 on the forceps. The unique device identifier (UDI) 10885403041006 is also listed on the packaging.
Look for the model number F-5006 and UDI 10885403041006 on the packaging or device.
The user manual is missing critical instructions for power supply and cleaning, which could lead to improper use.
No, but you should check the model number and UDI to confirm if your product is affected.
Carefusion has provided updated instructions in the attached V. Mueller Bipolar Forcep IFU.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0397-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0397-2023 from Carefusion. 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.
