Carefusion recalls specific neuro/spine bipolar forceps due to missing instructions for power supply and cleaning. Owners should check model 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 certain neuro/spine bipolar forceps because the instructions for use are incomplete. This could lead to improper cleaning or power supply issues if users follow outdated or missing instructions.
The missing instructions could result in improper cleaning or incorrect power supply connections. This might cause damage to the device or affect surgical safety if users rely on outdated guidance.
Medical professionals using these bipolar forceps for neurosurgery or spine procedures are most at risk. The recall affects specific models sold with the UDI/DI number 10885403040955.
Check for the model: Carefusion V. Mueller Neuro/Spine Jewelers BIPOLAR FORCEPS 0.4MM TIP, CURVED, #7, length 4-3/4" (120MM). The UDI/DI number 10885403040955 identifies the affected units.
Identify the UDI/DI number 10885403040955 on the device to confirm it is affected.
The recall is due to missing instructions for power supply and cleaning that could affect safe use.
Check for the UDI/DI number 10885403040955 on the device. Affected models include Carefusion V. Mueller Neuro/Spine Jewelers BIPOLAR FORCEPS 0.4MM TIP, CURVED, #7, length 4-3/4" (120MM).
The recall does not specify a remedy, so contact Carefusion directly for guidance.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0393-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0393-2023 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.
