Carefusion recalls bipolar forceps tips due to missing instructions for power supply and cleaning. Affected units have specific model and lot numbers. Consumers should 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 tips that lack critical instructions for power supply and cleaning. This could lead to improper use if users follow outdated or incomplete guidelines.
The missing instructions could result in 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 or death.
Healthcare professionals using these surgical tools are most at risk. The recall affects specific model numbers and lot ranges sold by Carefusion.
Check for the model number F-1304 and lot numbers starting with 10885403040849. These tips were sold with specific dimensions and are used in medical procedures.
Reach out to Carefusion for specific instructions on how to handle the recalled product.
The recall is due to missing instructions for power supply and cleaning that are critical for safe use.
No, but you should contact Carefusion for guidance on handling the recalled product.
The affected model is F-1304 with lot numbers starting with 10885403040849.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0387-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0387-2023 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.
