Carefusion recalls Cushing Bayonet Bipolar Forceps due to missing instructions for power supply and cleaning. Affected units have UDI/DI 10885403040702. 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 Cushing Bayonet Bipolar Forceps because the instructions for use are incomplete. This could lead to improper cleaning or power supply issues, which might cause damage or injury during medical procedures.
The missing instructions could lead to improper cleaning or power supply connections, potentially causing electrical issues or damage to the device. This might affect the safety of medical procedures if the forceps are not used correctly.
Medical professionals using these forceps for procedures are most at risk. Patients and caregivers may also be affected if the forceps are used incorrectly.
Check for the model number 0.7MM tip, 7-1/2" (190MM) length, and reference number F-1000. The unique device identifier (UDI/DI) 10885403040702 applies to all lots.
Review the attached V. Mueller Bipolar Forcep IFU for complete instructions on power supply and cleaning.
The Instructions For Use provided by Carefusion are missing content related to power supply and cleaning, which could lead to improper use.
Check the instructions for complete guidance on power supply and cleaning. Contact Carefusion for further assistance.
The recall does not specify a deadline for action.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0373-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0373-2023 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.
