Carefusion recalls titanium bipolar forceps with missing instructions for power supply and cleaning. Owners should contact Carefusion for details on safety and remedies.
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 instructions for connecting to power supplies and cleaning. This could lead to improper use or damage if users follow incomplete guidelines.
The missing instructions could lead to improper connection with power supplies or inadequate cleaning, potentially causing device malfunction or injury. However, the hazard does not involve immediate risks like fire or serious injury in normal use.
Medical professionals using these forceps for surgical procedures are most at risk. The recall affects specific models sold with UDI/DI numbers starting with 10885403041075.
Check for the model name 'CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS 1.5MM TIP OVERALL LENGTH 10-1/2" (265MM), REF F-5022'. The UDI/DI number starts with 10885403041075.
Reach out to Carefusion for specific instructions on handling the recalled product and any necessary remedies.
The recall is due to missing instructions for connecting to power supplies and cleaning, which could lead to improper use or device damage.
Contact Carefusion directly for guidance on the next steps, as the recall does not specify immediate action like stopping use.
The recall indicates a risk of improper use or damage, but it does not mention serious injury or immediate hazards in normal use.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0403-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0403-2023 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.
