Carefusion recalls specific bipolar forceps due to missing instructions for power supply and cleaning. Owners should check model 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 a specific type of bipolar forceps because the instructions for use are incomplete. This could lead to improper cleaning or power supply issues if users follow outdated or missing guidance.
The missing instructions could cause improper cleaning or incorrect power supply handling. This might lead to device damage or reduced effectiveness during medical procedures.
Medical professionals who use these forceps for procedures are most at risk. The recall affects specific models sold with certain serial numbers.
Check for the model name 'Cushing Bayonet Bipolar Forceps, 0.7MM tip, insulated irrigating overall length 7-1/2" (190MM)'. The recall includes specific serial numbers starting with 10885403040818.
Identify the product model and serial number to confirm if it is recalled.
The instructions for use are missing content related to power supply and cleaning, which could lead to improper handling.
Check the model and serial number to see if it is recalled; contact Carefusion for further guidance.
The recall does not provide a fix; users must check if they have the recalled model and contact Carefusion for instructions.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0384-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0384-2023 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.
