Carefusion recalls bipolar forceps with missing cleaning and power supply instructions. Owners should check model numbers and contact Carefusion for details.
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 cleaning and power supply use. This could lead to improper use if owners follow outdated or incomplete guidelines.
The missing instructions could lead to improper cleaning or power supply connections, potentially causing damage to the device or affecting surgical safety. However, the hazard is not described as causing immediate injury.
Medical professionals using the Carefusion bipolar forceps for surgical procedures are most at risk. Owners of the specific model number are affected.
Check for the model number 10885403040825 on the product. The forceps have a 1.0mm tip and 7-1/2" (190mm) length. All lots of this model are affected.
Look for the model number 1088:5403040825 on the product label.
The recall is due to missing cleaning and power supply instructions in the device's user manual, which could affect proper use.
The official notice does not specify a remedy, so contact Carefusion directly for guidance.
The hazard is described as missing instructions, not an immediate risk of injury, so the danger level is low.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0385-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0385-2023 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.
