Recall archive / FDA device enforcement
LITe Decompression Snake Arm, REF 48080230 — FDA record Z-0610-2024
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 Nov 1, 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
- LITe Decompression Snake Arm, REF 48080230
- Reason
- Product arm was manufactured with the incorrect clamp component. As a result, the affected product arm cannot attach to the arm post shaft.
- Classification
- Class II
- Recalling firm
- Stryker Spine
- Quantity
- 9
- Agency-reported status
- Ongoing
- Source record identifier
- Z-0610-2024
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 (GTIN): 07613327263909, lot # 227764. |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
US: MD, MI, NM, TX & OUS: Canada & France.
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Report date
- Dec 27, 2023
- Recall initiation date
- Nov 1, 2023
- Center classification date
- Dec 21, 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.