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 type of bipolar forceps due to missing instructions for power supply and cleaning. This could lead to improper use if the user doesn't follow the correct safety steps.
The missing instructions could lead to improper cleaning or power supply use, which might cause damage to the device or affect its safety during medical procedures.
Medical professionals using these forceps for procedures are most at risk. Owners of the specific model should check if they have the recalled product.
Check for the model name 'HARDY-STYLE BAYONET BIPOLAR FORCEPS, 0.5MM TIP, INSULATED OVERALL LENGTH 8-1/2" (215MM)'. The product has a UDI/DI number 10885403040740 and is in all lots.
Look for the model name and UDI/DI number 10885403040740 on the product.
The recall is due to missing instructions for power supply and cleaning that could affect safe use.
Check for the model name and UDI/DI number 10885403040740 on the product.
Contact Carefusion for 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-0377-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0377-2023 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.