Carefusion recalls specific lots of endoscopic surgical grasper devices due to potential cracking from manufacturing adhesive. Affected units have unique lot numbers and UDI codes. Consumers should contact Carefusion for details.
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 endoscopic surgical grasper devices because they may crack or break from improper adhesive use during manufacturing. This could lead to device failure during surgery, posing a risk to patients.
The grasper's rotation knob may crack or break due to a manufacturing defect involving adhesive use. This could cause the device to malfunction during surgery, potentially leading to injury or complications for patients.
Surgical teams and hospitals using the specific lot numbers mentioned in the recall. Patients undergoing procedures with this device are at risk if the grasper fails during surgery.
Check for the lot number B23 and UDI code 10885403160592 on the device. The product is a specific endoscopic surgical grasper model with the reference number SP90-7048.
Reach out to Carefusion directly to confirm if your device is affected and get instructions for next steps.
The recall specifies that specific lots may crack or break due to manufacturing defects, so affected units should not be used until contacted by Carefusion.
Check for the lot number B23 and UDI code 10885403160592 on the device. The product is a specific endoscopic surgical grasper model with reference number SP90-7048.
Contact Carefusion directly to confirm if your device is affected and get instructions for next steps.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-2423-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-2423-2023 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.
