MotoBand CP — Class II medical device recall Z-0212-2020
Terminated recall by CrossRoads Extremity Systems, LLC, reported 2019-10-30, distributed nationwide. Potentially includes a 3.0mm x 30mm screw instead of 3.0mm x 28mm screw.
| Recall number | Z-0212-2020 |
|---|---|
| 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 | 2019-09-19 |
| Classified | 2019-10-24 |
| Reported by FDA | 2019-10-30 |
| Terminated | 2021-12-02 |
| Distributed | Nationwide (US) |
| Quantity | 36 screws |
| Lot numbers | 500750 |
| Model numbers | 15PL-3028 |
Product
MotoBand CP, Poly-axial Locking Screw, 3.0mm x 28mm
Reason for recall
Potentially includes a 3.0mm x 30mm screw instead of 3.0mm x 28mm screw.
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-0212-2020. 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.