Carefusion recalls specific lots of Snowden-Pencer MIS Diamond-TOUCH Grasper Diamond Jaw Babcock 5mm surgical device due to potential rotation knob cracking from manufacturing adhesive.
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 Snowden-Pencer Diamond-TOUCH Grasper surgical devices because improper adhesive use during manufacturing may cause the rotation knob to crack. This could lead to device failure during surgery.
The rotation knob on specific lots may crack due to incorrect adhesive use in manufacturing. This could cause the device to malfunction during surgical procedures, but the risk is low as it only affects specific production batches.
Surgical professionals using the specific lot numbers of the Snowden-Pencer Diamond-TOUCH Grasper device are affected. The risk is low as the issue is limited to specific manufacturing lots.
Check the lot number on the device, which should be B23 for the recalled items. The product is a Snowden-Pencer Diamond-TOUCH Grasper Diamond Jaw Babcock 5mm, 32cm, ratcheted surgical device with UDI/DI 10885403159701.
Look for the lot number B23 on the device's label to confirm if it is recalled.
The recall is due to potential cracking or breaking of the rotation knob from incorrect adhesive use in manufacturing.
Check the lot number on the device; if it is B23, contact Carefusion for further instructions.
The recall indicates a potential for device malfunction, but the risk is low as it only affects specific manufacturing lots.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-2416-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-2416-2023 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.
