Carefusion recalls bipolar forceps with 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 bipolar forceps due to missing instructions for power supply and cleaning. This could lead to improper use if owners rely on incomplete guidance.
The missing instructions could lead to improper power supply connections or inadequate cleaning, potentially causing device malfunction or safety issues during medical procedures.
Medical professionals using the Carefusion bipolar forceps for procedures are most at risk. Owners of the specific model with the UDI/DI 10885403040856 are affected.
Check for the model name 'Carefusion V. Mueller SCOVILLE-GREENWOOD BAYONET IRRIGATING BIPOLAR FORCEPS INSULATED, 1.5MM TIP OVERALL LENGTH 7-3/4" (195MM)'. The UDI/DI code 10885403040856 identifies the affected units.
Identify the model and UDI/DI code to confirm if your forceps are affected.
The recall occurs because the Instructions For Use provided by Carefusion are missing content related to power supply and cleaning instructions.
Check for the model name and UDI/DI code 10885403040856 on the product label.
Contact Carefusion for guidance on next steps, as the recall does not include a specific remedy.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0388-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0388-2023 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.
