Carefusion recalls bipolar forceps with missing instructions for power supply and cleaning. Owners should check model and lot numbers to determine if affected. No immediate action needed but review instructions carefully.
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 power supply and cleaning. This could lead to improper use if the user doesn't follow the correct procedures.
The missing instructions could lead to improper cleaning or power supply connections, which might cause damage to the device or affect its performance during medical procedures. However, the hazard is not described as causing serious injury in normal use.
Medical professionals using the bipolar forceps for surgical procedures are most likely affected. The recall applies to specific models sold with certain lot numbers.
Check for the model: CareFusion V. Mueller ROUND HANDLE BAYONET BIPOLAR FORCEPS 1.0MM TIP OVERALL LENGTH 9-1/2" (240MM), REF F-5061. The recall covers all lots with UDI/DI 10885403041136.
Review the device's instructions for proper power supply and cleaning to ensure safe use.
No, the recall does not require stopping use. However, you should check the instructions for proper use.
The recall covers specific models with UDI/DI 10885403041136. Check the model and lot numbers to confirm if your device is affected.
The recall does not mention any repair or replacement options. The remedy is null, so no action is required beyond checking the instructions.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0404-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0404-2023 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.
