Carefusion recalls titanium insulated 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 titanium insulated bipolar forceps because their instructions for use are incomplete. This could lead to improper cleaning or power supply issues, but the recall does not specify immediate danger.
The missing instructions could result in improper cleaning or incorrect power supply connections. This might cause damage to the device or affect its safety during medical procedures.
Medical professionals who use these forceps for procedures are most at risk. The recall applies to specific model numbers sold in the U.S. during the product's lifetime.
Check for the model number F-5301 on the forceps. The product was sold with UDI/DI 1088540: 10885403041266 and all lots.
Look for the model number F-5301 and UDI/DI 10885403041266 on the forceps.
The recall is due to missing instructions for power supply and cleaning that could affect safe use.
Check the product details and contact Carefusion for guidance.
The recall does not specify a risk of injury, only incomplete instructions that could lead to improper use.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0413-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0413-2023 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.
