Carefusion recalls titanium bipolar forceps with missing instructions for power supply and cleaning. Owners should check model numbers and 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 lack critical instructions for power supply and cleaning. This could lead to improper use if owners follow outdated or incomplete guidelines.
The forceps lack instructions for connecting to power supplies and cleaning, which could cause improper use. Without clear guidance, users might damage equipment or risk infection.
Medical professionals using these forceps for surgery or procedures are most at risk. Owners of the specific model with UDI/DI 10885403040986 should check if they have the recalled item.
Check for the model name: CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS, 1.0MM TIP OVERALL LENGTH 8-1/2" (215MM), REF F-5002. The unique identifier UDI/DI 10885403040986 applies to all lots.
Look for the model number on the product label to confirm if it matches the recalled CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS.
Reach out to Carefusion directly for further instructions on the recall and any necessary actions.
The recall is due to missing instructions for power supply connection and cleaning, which could lead to improper use.
Check for the model name and unique identifier UDI/DI 10885403040986 on the product label.
No, the recall does not require immediate discontinuation; contact Carefusion for specific instructions.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0396-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0396-2023 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.
