Carefusion recalls specific lots of endoscopic surgical grasper models due to potential rotation knob cracking from manufacturing adhesive issues. Affected units have unique identifiers; 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 endoscopic surgical graspers because the rotation knob might crack due to a manufacturing adhesive issue. This could lead to device failure during surgery if not fixed.
The rotation knob in specific lots can crack due to a manufacturing adhesive issue. This might cause the grasper to malfunction during surgery, potentially leading to device failure or injury.
Surgical teams using the specific model of endoscopic grasper with lot number B23 are most at risk. Patients and medical staff using the recalled product may face device failure during procedures.
Check for the model name 'Snowden-Pencer MIS DIAMOND-TOUCH GRASPER MCKERNAN FUNDUS 5MM, 32CM, RATCHETED' and lot number B23 on the device. The unique identifier (UDI/DI) 10885403159671 also identifies affected units.
Look for the model name and lot number B23 on the device to confirm if it's affected.
The recall only affects specific lots with lot number B23; other units are safe.
Check the device for the model name and lot number B23. If affected, contact Carefusion for instructions.
Check the unique identifier (UDI/DI) 10885403159671 and lot number B23 on the device.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-2415-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-2415-2023 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.
