Carefusion recalls bipolar forceps with missing instructions for power supply and cleaning. Owners should check 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 a specific model of bipolar forceps due to missing 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 This could lead to improper use if users follow outdated or incomplete guidelines.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 handling, potentially causing damage to the device or affecting surgical safety. However, the hazard does not involve immediate risks like injury or fire.
Medical professionals using these forceps for surgical procedures are most at risk. The recall affects all units of this specific model sold with the UDI/DI 10885403041167.
Check for the model name 'CareFusion V. Mueller ROUND HANDLE BAYONET BIPOLAR FORCEPS 0.7MM TIP OVERALL LENGTH 10-1/2" (265MM), REF F-5067' and the UDI/DI 10885403041167 on the product.
Identify the model and UDI/DI number to confirm if your forceps are affected.
The recall is due to missing instructions for power supply and cleaning that are present in the manufacturer's original instructions.
No, the recall does not require immediate discontinuation. However, you should check the product details to confirm if it is affected.
The manufacturer has provided a reference to the V. Mueller Bipolar Forcep IFU for additional instructions.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0405-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0405-2023 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.
