Carefusion recalls specific Cushing Bipolar Forceps due to 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 a specific model of Cushing Bipolar Force: the 1.5mm tip, insulated forceps with 7-inch length (ref F-2002). The recall is because the instructions for use are incomplete, which could lead to improper cleaning or power supply issues.
The missing instructions could lead to improper cleaning or incorrect power supply use, potentially causing damage to the device or safety issues during medical procedures. However, the hazard is not described as causing serious injury in normal use.
Healthcare professionals using these surgical tools are most at risk. The recall affects all units of this specific model sold with the UDI/DI 10885403040900.
Check for the model name 'Cushing Bipolar Forceps 1.5MM TIP, INSULATED OVERALL LENGTH 7" (180MM)' and the reference number F-2002. The recall includes all units with UDI/DI 10885403040900.
Identify the model and reference number to confirm if your device is affected.
Reach out to Carefusion for specific guidance on next steps.
The recall is due to missing instructions for use related to power supply and cleaning, which could lead to improper use.
Check for the model 'Cushing Bipolar Forceps 1.5MM TIP, INSULATED OVERALL LENGTH 7" (180MM)' and reference number F-2002 with UDI/DI 10885403040900.
Contact Carefusion for specific 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-0390-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0390-2023 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.
