Recall archive / FDA device enforcement
Snowden-Pencer MIS DIAMOND-TOUCH CLAMP BOWEL 60 MM JAW 5MM, 32CM, RATCHETED, REF SP90-7046; endoscopic surgical device — FDA record Z-2422-2023
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Jul 13, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Snowden-Pencer MIS DIAMOND-TOUCH CLAMP BOWEL 60 MM JAW 5MM, 32CM, RATCHETED, REF SP90-7046; endoscopic surgical device
- Reason
- 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.
- Classification
- Class II
- Recalling firm
- Carefusion 2200 Inc
- Quantity
- 4 units
- Agency-reported status
- Ongoing
- Source record identifier
- Z-2422-2023
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | UDI/DI 10885403160578, Lot Numbers: C23, L22 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
US and Canada
No US distribution state could be established from this record. Check the official notice.
Dates in the source
- Report date
- Aug 23, 2023
- Recall initiation date
- Jul 13, 2023
- Center classification date
- Aug 17, 2023
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.