Carefusion recalls bipolar forceps with missing instructions for power supply and cleaning. Owners should check model and lot numbers to determine if affected.
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 bipolar forceps that lack critical instructions for power supply and cleaning. This could lead to improper use if owners don't follow the missing safety steps.
The forceps lack instructions for connecting to power supplies and cleaning, which could cause improper use. Without these steps, there's a risk of damage or injury during medical procedures.
Medical professionals using these forceps for surgery or procedures are most at risk. Owners must check their model and lot numbers to see if they are affected.
Check for the model number 'Carefusion V. Mueller SEMKIN BIPOLAR FORCEPS 1.5MM TIP, INSULATED OVERALL LENGTH 6" (150MM), REF F-1045' and lot numbers starting with 10885403040764.
Look for the model number 'Carefusion V. Mueller SEMKIN BIPOLAR FORCEPS 1.5MM TIP, INSULATED OVERALL LENGTH 6" (150MM), REF F-1045' and lot numbers starting with 10885403040764.
No, but you should check if your forceps are affected by the recall. The recall requires checking model and lot numbers, not immediate discontinuation.
Check the model and lot numbers to see if they match the recalled items. If affected, you may need to contact Carefusion for instructions.
The recall states missing instructions for power supply and cleaning, which could lead to improper use during medical procedures.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0379-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0379-2023 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.
