Carefusion recalls specific lots of Diamond-Touch Clamp Debakey 35mm Jaw 5mm surgical devices due to potential rotation knob cracking from manufacturing adhesive issues. Affected units have UDI 10885403160554 and lots B23/C23.
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 Diamond-Touch Clamp Debakey surgical devices because the rotation knob may crack due to a manufacturing defect. This could pose a risk during surgery if the clamp fails unexpectedly.
The rotation knob may crack during use because of a manufacturing defect involving incorrect adhesive application. This could lead to the clamp failing unexpectedly during surgery, potentially causing injury to the patient or surgeon.
Surgical professionals using the specific recalled Diamond-Touch Clamp Debakey devices with UDI 10885403160554 and lots B23/C23 are most at risk. Patients and other healthcare workers are not directly affected by this recall.
Check for the UDI number 10885403160554 and lot numbers B23 or C23 on the device packaging or label. The product is a Diamond-Touch Clamp Debakey 35mm Jaw 5mm endoscopic surgical device.
Look for the UDI number 10885403160554 and lot numbers B23 or C23 on the device packaging or label.
The rotation knob may crack due to a manufacturing defect involving incorrect adhesive application, which could cause the clamp to fail unexpectedly during surgery.
Check for the UDI number 10885403160554 and lot numbers B23 or C23. If you have these details, contact Carefusion for further instructions.
While the defect could cause the clamp to fail during surgery, the risk is low as this affects specific manufacturing lots and not all units.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-2420-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-2420-2023 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.
