Class II — Crossroads Extremity Systems Llc
| Recalling firm | CrossRoads Extremity Systems LLC |
|---|---|
| Registered facility | CROSSROADS EXTREMITY SYSTEMS LLC (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Seven 18mm x 18mm x 18 mm implants had been placed in kits, packed and labeled as 18mm x 14mm x 14mm. |
| Product | MotoCLIP(TM) Super Elastic Fusion System, Size 18mm x 14mm x 14mm, REF 1442-1814, Rx Only, STERILE R. |
| Quantity | 20 units |
| Distribution | Al, FL, IN, Il, NE, TX, NM, CO, AZ |
| Initiated | 2017-02-16 |
| Classified | 2017-03-20 |
| Terminated | 2017-04-27 |
| Recall number | Z-1487-2017 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Crossroads Extremity Systems Llc (Z-1487-2017).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/76687/
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