Carefusion recalls specific lots of endoscopic surgical grasper models due to potential rotation knob cracking from manufacturing adhesive issues. Affected units have unique lot numbers and UDI codes.
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 their endoscopic surgical grasper devices because improper adhesive use during manufacturing could cause the rotation knob to crack. This poses a risk of the device failing during surgery, potentially causing injury to patients.
The rotation knob may crack due to a manufacturing defect involving adhesive application. If the knob cracks during use, it could cause the grasper to malfunction, potentially leading to injury to surgical patients.
Surgical teams using the specific model of endoscopic grasper with lot number B23 are most at risk. Patients undergoing procedures with this device could face complications if the grasper fails.
Check for the lot number B23 on the device's packaging or label. The unique UDI code 10885403159725 identifies the affected units. This device is sold under the model name 'Snowden-Pencer MIS DIAMOND-TOUCH ATRAUMATIC GRASPER DIAMOND JAW 5MM, 32CM, RATCHETED.'
Look for the lot number B23 or UDI code 10885403159725 on the device packaging or label.
The recall is due to potential cracking of the rotation knob caused by an adhesive issue during manufacturing.
Check for lot number B23 or UDI code 10885403159725 on the device packaging or label.
The recall record 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-2417-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-2417-2023 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.
