Carefusion recalls bipolar forceps with missing instructions for power supply and cleaning. Owners should check model and lot numbers for affected units.
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 a specific type of bipolar forceps due to missing instructions for power supply and cleaning. This could lead to improper use if the user doesn't follow the correct procedures.
The missing instructions could lead to improper cleaning or power supply handling, which might cause damage to the device or affect its safety. However, the hazard is not described as causing serious injury in normal use.
Medical professionals using these forceps for procedures are most at risk. The recall affects specific models sold with certain lot numbers.
Check for the model: CareFusion V. Mueller ROUND HANDLE BAYONET BIPOLAR FORCEPS, 1.0MM TIP OVERALL LENGTH 10-1/2" (265MM), REF F-5069. Affected units have UDI/DI 10885403041174 and all lots.
Look for the model number and UDI/DI 10885403041174 on the product to confirm if it is affected.
The recall is due to missing instructions for power supply and cleaning that are in the manufacturer's instructions but not in the provided user manual.
Check for the model: CareFusion V. Mueller ROUND HANDLE BAYONET BIPOLAR FORCEPS, 1.0MM TIP OVERALL LENGTH 10-1/2" (265MM), REF F-5069 with UDI/DI 10885403041174 and all lots.
The recall does not specify a remedy, so contact Carefusion for further instructions.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0406-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0406-2023 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.
