Recall archive / FDA device enforcement
EasyFuse Dynamic Compression System Instrument Pack — FDA record Z-0853-2022
Reported terminated
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 Mar 10, 2022. 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
- EasyFuse Dynamic Compression System Instrument Pack
- Reason
- The drill and adjustable drill guide can jam/bind intraoperatively resulting in the drill guide breaking.
- Classification
- Class II
- Recalling firm
- Wright Medical Technology, Inc.
- Quantity
- 176 packs
- Agency-reported status
- Terminated
- Source record identifier
- Z-0853-2022
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 | Model Number FFSP1530, UDI: 00889797103565 Lot Codes (Expiration Date): 781853-110321 (11/03/2029) and 780395-112221 (12/03/2029) |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
US distribution to Florida, North Carolina, Ohio, and Texas
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
- Apr 6, 2022
- Recall initiation date
- Mar 10, 2022
- Center classification date
- Mar 31, 2022
- Termination date
- Apr 1, 2026
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.