Carefusion recalls bipolar forceps with missing cleaning and power supply instructions. 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 bipolar forceps that lack critical cleaning and power supply instructions. This could lead to improper use if owners follow outdated or incomplete instructions.
The missing instructions could result in improper cleaning or power supply connections, potentially causing damage to the device or affecting surgical safety.
Medical professionals using these forceps for surgery or procedures. Those with the specific model and lot numbers are most at risk.
Check for the model: Carefusion V. Mueller GERALD BAYON: Bipolar Forceps 1.0MM Tip, 7-1/2" (190MM) with reference number F-1111. All lots are affected.
Identify the model and lot number to confirm if your forceps are affected.
The recall is due to missing cleaning and power supply instructions in the device's user manual.
Check for the model: Carefusion V. Mueller GERALD BAYONET BIPOLAR FORCEPS 1.0MM TIP, OVERALL LENGTH 7-1/2" (190MM), REF F-1111. All lots are affected.
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-0381-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0381-2023 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.