MotoCLIP — Class II medical device recall Z-1487-2017
Terminated recall by Crossroads Extremity Systems Llc, reported 2017-03-29, distributed in AZ, CO, FL, IN, NE, NM, TX. Seven 18mm x 18mm x 18 mm implants had been placed in kits, packed and labeled as 18mm x 14mm x 14mm.
| Recall number | Z-1487-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Crossroads Extremity Systems Llc, Memphis, TN, United States |
| Recall initiated | 2017-02-16 |
| Classified | 2017-03-20 |
| Reported by FDA | 2017-03-29 |
| Terminated | 2017-04-27 |
| Distributed | AZ, CO, FL, IN, NE, NM, TX |
| Quantity | 20 units |
| Reason classes | labeling |
| Lot numbers | 101868 |
| Model numbers | 1442-1814 |
Product
MotoCLIP(TM) Super Elastic Fusion System, Size 18mm x 14mm x 14mm, REF 1442-1814, Rx Only, STERILE R.
Reason for recall
Seven 18mm x 18mm x 18 mm implants had been placed in kits, packed and labeled as 18mm x 14mm x 14mm.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1487-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.