Carefusion 2200 recalls specific lots of their Snowden-Pencer MIS Diamond-Touch Dissector Diamond Jaw 5mm surgical device for potential rotation knob cracking from manufacturing adhesive issues.
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 2200 is recalling specific lots of their Snowden-Pencer MIS Diamond-Touch Dissector Diamond Jaw 5mm surgical device because improper adhesive use during manufacturing could cause the rotation knob to crack. This poses a risk of the device failing during surgery, which could lead to complications for patients.
The rotation knob on specific lots may crack due to incorrect adhesive use in manufacturing. If the knob cracks during surgery, it could fail to function properly, potentially causing injury to patients or complications during the procedure.
Surgical teams using the specific lots of Snowden-Pencer MIS Diamond-Touch Dissector Diamond Jaw 5mm endoscopic devices. Surgeons and medical staff are most at risk if the device cracks during use.
Check for lot numbers L22, B23, or C23 on the device's packaging or label. The product is a Snowden-Pencer MIS Diamond-Touch Dissector Diamond Jaw 5mm endoscopic surgical device with reference number SP90-7071.
Look for lot numbers L22, B23, or C23 on the device's packaging or label.
Specific lots of the product have the potential to crack or break due to incorrect adhesive use in manufacturing.
Check the lot number on the device. If it's L22, B23, or C23, contact Carefusion 2200 for further instructions.
The device could crack during use, potentially causing failure during surgery, which may lead to complications for patients.
We’ve drafted a message you can send Carefusion 2200 to request your refund or repair — edit it as you like.
Subject: Recall Z-2425-2023 — Carefusion 2200 Carefusion 2200 Hello, I own a Carefusion 2200 that is covered by recall Z-2425-2023 from Carefusion 2200. 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.
