Carefusion recalls bipolar forceps with missing instructions for power supply and cleaning. 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 bipolar forceps that lack critical instructions for power supply and cleaning. This could lead to improper use if owners follow outdated or incomplete guidelines.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, which might cause damage or safety issues during medical procedures. However, the hazard is not described as causing serious injury in normal use.
Medical professionals using these forceps for procedures are most at risk. Owners of the specific model number must check if they have the recalled item.
Check for the model number 10885403040771 on the product. The forceps have a 1.0mm wide tip and 7-inch length. They were sold with the reference number F-1110.
Look for the model number 10885403040771 on the forceps or packaging.
The recall is due to missing instructions for power supply and cleaning, which could lead to improper use.
Check the model number and contact Carefusion for further instructions.
The recall states the missing instructions could lead to improper use, but it does not specify a risk of serious injury in normal use.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0380-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0380-2023 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.
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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.
