Carefusion recalls specific neuro/spine forceps due to missing instructions for power supply and cleaning. Owners should check model and lot numbers to determine if affected.
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 their instructions for use are incomplete. This means users might not know how to safely clean or connect the device to power, which could lead to improper use.
The missing instructions could lead to improper cleaning or power connections. This might cause damage to the device or affect its performance during medical procedures, but it does not pose an immediate risk of injury.
Medical professionals using these forceps for spinal procedures are most likely affected. Patients and caregivers are not at risk since the issue is with the instructions, not the device itself.
Check for the model: CareFusion V. Mueller Neuro/Spine TITANUIM BIPOLAR FORCEPS STRAIGHT, 0.25MM TIP OVERALL LENGTH 6" (150MM), REF F-5128. The lot numbers are all listed as UDI/DI 10885403041242.
Look for the model number and lot number on the device or packaging to confirm if it is affected.
The recall is happening because the instructions for use are missing content related to power supply and cleaning, which could affect safe use.
No, the recall does not require stopping use. The issue is with the instructions, not the device itself.
Check for the model number and lot number on the device or packaging. Affected units have the model: CareFusion V. Mueller Neuro/Spine TITANUIM BIPOLAR FORCEPS STRAIGHT, 0.25MM TIP OVERALL LENGTH 6" (150MM), REF F-5128, and lot number UDI/DI 10885403041242.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0412-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0412-2023 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.
