Snowden-pencer MIS Diamond-touch Atraumatic Grasper recall
Snowden-Pencer MIS DIAMOND-TOUCH ATRAUMATIC GRASPER DIAMOND JAW 5MM, 32CM, RATCHETED, REF SP90-7020; endoscopic surgical device
Why was Snowden-pencer MIS Diamond-touch Atraumatic Grasper recalled?
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.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI/DI 10885403159725, Lot Number B23
- Product
- Snowden-Pencer MIS DIAMOND-TOUCH ATRAUMATIC GRASPER DIAMOND JAW 5MM, 32CM, RATCHETED, REF SP90-7020; endoscopic surgical device
- Recalling firm
- Carefusion 2200 Inc
- Quantity
- 1 unit
- Distribution
- US and Canada
- Recall date
- August 23, 2023
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)