Carefusion recalls specific lots of endoscopic surgical clamps due to potential cracking from manufacturing adhesive. Affected units may break during use, causing injury. 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 clamps that could crack during use due to a manufacturing defect. This poses a risk of injury if the clamp breaks while in operation.
The clamps may crack or break during use because of an incorrect adhesive used in manufacturing. This defect could lead to the clamp failing while in operation, potentially causing injury to the patient or surgical staff.
Surgical professionals using the specific lot numbers of the Snowden-Pencer MIS DIAMOND-TOUCH CLAMP BOWEL 60 MM JAW 5MM, 32CM, RATCHETED model. Patients undergoing procedures with this device are at risk if the clamp breaks during surgery.
Check for the model name 'Snowden-Pencer MIS DIAMOND-TOUCH CLAMP BOWEL 60 MM JAW 5MM, 32CM, RATCHETED' and lot numbers C23 or L22. The device has a unique identifier (UDI/DI) 10885403160578.
Look for lot numbers C23 or L22 on the device's packaging or label.
Reach out to Carefusion directly for further instructions on the recall.
The clamps may crack or break during use due to an incorrect adhesive used in manufacturing.
Check the lot number on the device; if it's C23 or L22, contact Carefusion for instructions.
Yes, the defect could cause the clamp to break during surgery, potentially leading to injury.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-2422-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-2422-2023 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.
