Carefusion 2200 Inc recalls specific lots of Snowden-Pencer MIS Diamond-Touch Dissector Diamond Jaw 5mm surgical devices due to 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 Inc is recalling specific lots of their Snowden-Pencer MIS Diamond-Touch Dissector Diamond Jaw 5mm endoscopic surgical devices. The devices could crack or break due to a manufacturing defect involving adhesive use, which might cause injury during surgery.
The rotation knob on specific lots of these surgical devices may crack or break because of an incorrect adhesive used during manufacturing. This defect could potentially cause injury during surgical procedures if the device breaks unexpectedly.
Surgical professionals using the specific lot numbers (B23, C23) of the Snowden-Pencer MIS Diamond-Touch Dissector Diamond Jaw 5mm endoscopic surgical device are most at risk. This recall affects only the listed lots.
Check for the lot numbers 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 SP90-7271.
Look for lot numbers 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 B23 or C23, contact Carefusion 2200 Inc for instructions.
The recall states the device could crack or break, but no specific injury risk is mentioned in the official notice.
We’ve drafted a message you can send Carefusion 220:00 to request your refund or repair — edit it as you like.
Subject: Recall Z-2429-2023 — Carefusion 220:00 Carefusion 220:00 Hello, I own a Carefusion 220:00 that is covered by recall Z-2429-2023 from Carefusion 220:00. 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.
