Carefusion 2200 recalls specific lots of their Snowden-Pencer MIS Diamond-Touch Clamp due to potential rotation knob cracking from manufacturing adhesive issues. Affected units have lot numbers L22, B23, C23.
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 surgical clamps because the rotation knob might crack due to a manufacturing defect. This could lead to equipment failure during surgery if not addressed.
The rotation knob in specific lots may crack because of an incorrect adhesive used during manufacturing. This could cause the clamp to malfunction during surgery, potentially leading to equipment failure or injury.
Surgical teams using the specific lot numbers L22, B23, or C23 of the Snowden-Pencer MIS Diamond-Touch Clamp. Surgeons and medical staff are most at risk during procedures.
Check for lot numbers L22, B23, or C23 on the product's packaging or documentation. The product is a Snowden-Pencer MIS Diamond-Touch Clamp with model reference SP90-7043.
Look for lot numbers L22, B23, or C23 on the product's packaging or documentation.
Lot numbers L22, B23, and C23.
Specific lots have a potential risk of the rotation knob cracking due to an incorrect adhesive used in manufacturing.
Check for lot numbers L22, B23, or C23 on the product's packaging or documentation. The product is a Snowden-Pencer MIS Diamond-Touch Clamp with model reference SP90-7043.
We’ve drafted a message you can send Carefusion 2200 to request your refund or repair — edit it as you like.
Subject: Recall Z-2419-2023 — Carefusion 2200 Carefusion 2200 Hello, I own a Carefusion 2200 that is covered by recall Z-2419-2023 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.
