Carefusion recalls specific Cushing Micro 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 Cushing Micro 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 This could lead to improper cleaning or power supply issues if users follow outdated or missing guidance.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 result in improper cleaning or incorrect power supply connections, potentially causing device malfunction. However, the hazard does not involve immediate risks like injury or fire.
Medical professionals using the specific model of Cushing Micro Bipolar Forceps for surgical procedures are most at risk. The recall affects all units with the model number F-52000.
Check for the model number F-52000 on the device. The product has a specific length of 6 inches (150mm) and a UDI/DI code of 10885403041297.
Identify the model number F-52000 and UDI/DI code 10885403041297 to confirm if your device is affected.
The recall is due to missing instructions for power supply and cleaning, which could lead to improper use.
Check the model number and UDI/DI code to confirm if it's affected; contact Carefusion for further instructions.
The hazard is low risk as it involves incomplete instructions, not immediate injury or fire risks.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0417-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0417-2023 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.
