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 have incomplete instructions for connecting to power supplies and cleaning. This could lead to improper use or damage if users follow outdated or missing guidance.
The forceps lack critical instructions for connecting to power supplies and cleaning. Without these, users might damage equipment or cause injury through improper maintenance.
Medical professionals using these forceps for surgical procedures are most at risk. The recall affects specific model numbers sold with UDI/DI 10885403041068.
Check for the model number 10885403041068 on the product's UDI/DI label. The forceps have a titanium round handle and 1.0mm tip with an overall length of 10-1/2 inches (265mm).
Look for the UDI/DI number 10885403041068 on the forceps to confirm if it's affected.
The recall is due to missing instructions for connecting to power supplies and cleaning the forceps, which could lead to improper use.
Check for the UDI/DI number 10885403041068 on the product's label; the forceps have a titanium round handle and 1.0mm tip with an overall length of 10-1/2 inches (265mm).
The recall does not specify a remedy, so contact Carefusion directly for guidance on next steps.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0402-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0402-2023 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.
