Carefusion recalls specific lots of Snowden-Pencer MIS Diamond-Touch Graspers due to potential cracking from manufacturing adhesive. Affected units have UDI 10885403160769 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 MIS Diamond-Touch Graspers that could crack due to a manufacturing adhesive issue. This risk could lead to device failure during use, especially in surgical settings.
The rotation knob in specific lots may crack or break because of an incorrect adhesive used during manufacturing. This could cause the device to malfunction during surgery, potentially leading to unintended movement or failure.
Surgical professionals using the Snowden-Pencer MIS Diamond-Touch Graspers with UDI 10885403160769 and Lot B23 are most at risk. The recall affects specific surgical tools used in endoscopic procedures.
Check for the UDI number 10885403160769 and Lot Number B23 on the device. This specific model is used in endoscopic surgery and has a ratcheted handle.
Look for the UDI number 10885403160769 and Lot Number B23 on the device.
The specific lots of Snowden-Pencer MIS Diamond-Touch Graspers have a potential risk of cracking or breaking due to an incorrect adhesive used in manufacturing.
Check for the UDI number 10885403160769 and Lot Number B23 on the device.
The recall record does not specify a remedy, so contact Carefusion directly for further instructions.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-2424-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-2424-2023 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.
