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 connecting to power supplies and cleaning. This could lead to improper use if the user doesn't follow the correct procedures.
The missing instructions could lead to improper connection to power supplies or inadequate cleaning, which might cause equipment malfunction or infection risks. However, the hazard is not described as causing immediate injury or death.
Medical professionals using the Carefusion bipolar forceps for surgical procedures are most at risk. The recall affects all units of this specific model sold with the UDI/DI 10885403041198.
Check for the model name 'CareFusion V. Mueller ROUND HANDLE BAYONET BIPOLAR FORCEPS 1.5MM TIP OVERALL LENGTH 10-1/2" (265MM), REF F-5073' and the UDI/DI number 10885403041198 on the product packaging.
Look for the model number and UDI/DI code on the product packaging to confirm if it is recalled.
The recall is due to missing instructions for connecting to power supplies and cleaning the device, which could lead to improper use.
Check the product details to see if it matches the recalled model. Contact Carefusion for further guidance.
The recall states the missing instructions could lead to improper use, but it does not specify a risk of injury or death.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0407-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0407-2023 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
