Carefusion recalls titanium bipolar forceps due to 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 titanium bipolar spinal forceps because their instructions for use are incomplete. This could lead to improper cleaning or power supply issues if users follow outdated or missing guidelines.
The missing instructions could result in improper cleaning or incorrect power supply connections. This might cause damage to the device or pose a risk during medical procedures if users rely on outdated guidance.
Medical professionals using these spinal surgical tools are most at risk. The recall affects specific models sold with UDI/DI numbers starting with 10885403041020.
Check for the model name 'CareFusion V. Mueller Neuro/Spine TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS' with a 1.0mm tip and 9-1/2" length. The UDI/DI number 10885403041020 is listed for all affected lots.
Verify the model name and UDI/DI number to confirm if your forceps are affected.
The instructions for use are missing content related to power supply and cleaning, which could lead to improper use.
Check for the model name and UDI/DI number 10885403041020 on the product label.
Contact Carefusion for guidance on next steps, as the recall does not include a specific remedy.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0399-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0399-2023 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.
