Carefusion 2200 recalls specific lots of their Diamond-Touch Bowel Clamp for potential rotation knob cracking from manufacturing adhesive issues. Affected units have UDI/DI 10885403160561 and Lot B23. Contact for remedy.
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 Diamond-Touch Bowel Clamps that may crack due to a manufacturing adhesive issue. This could lead to the clamp failing during surgery, posing a risk to patients and surgical teams.
The rotation knob on specific lots may crack or break because of an incorrect adhesive used during manufacturing. This could cause the clamp to malfunction during surgery, potentially leading to tissue damage or procedural failure.
Surgical teams and hospitals using Carefusion 2200's Diamond-Touch Bowel Clamps with UDI/DI 10885403160561 and Lot B23 are most at risk. Patients undergoing endoscopic procedures with these clamps could face complications.
Check for the UDI/DI number 10885403160561 and Lot Number B23 on the clamp's packaging or label. This specific model is used in endoscopic surgical procedures.
Verify the UDI/DI number 10885403160561 and Lot Number B23 on the clamp's packaging or label.
This recall applies only to specific lots with UDI/DI 10885403160561 and Lot B23. Check your clamp's label to see if it's affected.
The recall record does not specify a remedy, so contact Carefusion 2200 directly for guidance.
The recall states the clamp may crack or break, which could lead to surgical complications. However, the exact risk level is not specified in the record.
We’ve drafted a message you can send Carefusion 2200 to request your refund or repair — edit it as you like.
Subject: Recall Z-2421-2023 — Carefusion 2200 Carefusion 2200 Hello, I own a Carefusion 2200 that is covered by recall Z-2421-2023 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.
