Carefusion recalls specific bipolar forceps due to 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 a specific model of bipolar forceps because the instructions for use are incomplete. This means users might not know how to safely clean or connect the device to power, which could lead to improper use.
The missing instructions could lead to improper cleaning or power connections, potentially causing device malfunction. However, the hazard does not involve immediate risks like injury or fire.
Medical professionals who use these bipolar forceps for surgical procedures are most at risk. The recall affects specific model numbers sold with a particular UDI/DI code.
Check for the model number 'CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS 1.5MM TIP OVERALL LENGTH 9-1/2" (240MM), REF F-5014' and UDI/DI code 10885403041044. This product was sold in all lots.
Identify the model number and UDI/DI code to confirm if your forceps are affected.
The recall is because the Instructions For Use provided by Carefusion are missing content related to power supply and cleaning instructions.
Check the model number and UDI/DI code to see if it's affected. Contact Carefusion for further instructions.
The hazard does not involve immediate risks like injury or fire; it's a low-risk issue due to incomplete instructions.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0400-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0400-2023 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.
