Carefusion recalls titanium bipolar forceps with missing instructions for power supply and cleaning. Owners should check product details and contact Carefusion for guidance.
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 incomplete instructions for connecting to power supplies and cleaning. This could lead to improper use or damage if users follow outdated instructions.
The missing instructions could cause improper power connections or cleaning, potentially leading to device damage or unsafe use. However, the hazard does not involve immediate risks like injury or fire.
Medical professionals using these forceps for procedures are most at risk. Patients and caregivers should check if they own the recalled model.
Check for the model: CareFusion V. Mueller TITANI: 1.0MM TIP, STR, MED, INSULATED OVERALL. The product has a UDI/DI number 10885403041280 across all lots.
Identify the model and UDI/DI number to confirm if your forceps are recalled.
The recall is due to missing content in the Instructions For Use related to power supply and cleaning.
Look for the model: CareFusion V. Mueller TITANIUM BAYONET INSULATED IRRIGATING BIPOLAR FORCEPS 1.0MM TIP, STR, MED, INSULATED OVERALL with UDI/DI 10885403041280 across all lots.
The recall does not specify a remedy, so contact Carefusion for guidance.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0415-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0415-2023 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.
