Carefusion recalls titanium bipolar forceps due to missing power supply and cleaning instructions in user manuals. Affected models include F-5125 with UDI 10885403041211. Consumers should check their 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 bipolar forceps that lack critical instructions for power supply and cleaning. This could lead to improper use or damage if users follow outdated or incomplete manuals.
The missing instructions could cause improper power connections or inadequate cleaning, potentially leading to device malfunction or infection risks. However, the hazard is not described as causing immediate injury or death.
Medical professionals using these forceps for surgery or procedures are most at risk. The recall affects specific models sold with UDI 10885403041211.
Check for the model number F-5125 and UDI 10885403041211 on the product. These forceps are sold under Carefusion's brand with the specified dimensions.
Look for the model number F-5125 and UDI 10885403041211 on the forceps to confirm if they are affected.
The recall is due to missing power supply and cleaning instructions in the user manual, which could lead to improper use or device damage.
Check for the model number F-5125 and UDI 10885403041211 on the product. These specific forceps are affected by the recall.
The recall does not specify a remedy, so contact Carefusion directly for guidance on next steps.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0409-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0409-2023 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.
