Carefusion recalls specific lots of Diamond-Touch Clamp Debakey 25mm jaw surgical devices due to potential cracking from manufacturing adhesive. Affected units may break during use.
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 Diamond-Touch Clamp Debakey surgical devices because they might crack or break during use due to a manufacturing adhesive issue. This could cause injury during surgery if the device fails.
The device's rotation knob may crack or break during use because of a manufacturing defect involving adhesive. This could lead to the clamp malfunctioning during surgery, potentially causing injury to the patient or surgical team.
Surgical teams using the specific lot numbers of this endoscopic device are most at risk. Patients undergoing procedures with these devices could face complications if the clamp fails.
Check for the lot number B23 on the device's packaging or label. The specific model is the Diamond-Touch Clamp Debakey 2:5mm jaw, 45cm, ratcheted, with reference number SP90-7243.
Look for lot number B23 on the device's packaging or label to confirm if it's affected.
Reach out to Carefusion for assistance with the recall process if you have the affected device.
The device may crack or break during use due to a manufacturing adhesive issue that could cause failure during surgery.
Check the lot number on the device; if it's B23, contact Carefusion for assistance.
The device may not be safe to use as it could crack or break during surgery, so check the lot number first.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-2427-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-2427-2023 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.
