Carefusion recalls specific lots of Snowden-Pencer MIS Diamond-Touch Dissector due to potential rotation knob cracking from manufacturing adhesive issues. Affected units have UDI 10885403159862 and Lot B23. Contact Carefusion for details.
Specific lots of the product have the potential to exhibit cracking or breaking of the rotation knob due to the incorrect use of an adhesive in the manufacturing process.
Carefusion is recalling specific lots of Snowden-Pencer surgical dissectors that may crack due to a manufacturing defect. This could cause injury during surgery if the device breaks unexpectedly.
The rotation knob on specific lots can crack or break during use because of an adhesive defect in manufacturing. This could lead to the device malfunctioning during surgery, potentially causing injury to the patient or surgeon.
Surgical professionals using the Snowden-Pencer MIS Diamond-Touch Dissector in endoscopic procedures are most at risk. Patients undergoing surgery with this specific model may be affected.
Check for the UDI number 10885403159862 and Lot Number B23 on the device. This specific model is used in endoscopic surgery and has a non-ratchet design.
Look for the UDI number 10885403159862 and Lot Number B23 on the device to confirm if it's affected.
Specific lots of the Snowden-Pencer MIS Diamond-Touch Dissector may have a rotation knob that cracks or breaks due to a manufacturing adhesive defect.
Check for the UDI number 10885403159862 and Lot Number B23 on the device. This specific model is used in endoscopic surgery.
The recall record does not specify a remedy, so contact Carefusion directly for instructions.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-2418-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-2418-2023 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.
