FDA Device recall Z-1490-2015
CROSSCHECK(R) Plating system, MTP NX Plate, Left, Recon, REF CCP-MPN2L. Orthopedic use
- FDA Device
- Class II
- terminated
- Published 2015-04-29
On 2015-04-29 the FDA classified a Class II recall of CROSSCHECK(R) Plating system, MTP NX Plate, Left, Recon, REF CCP-MPN2L. Orthopedic use by Wright Medical Technology, citing the minor diameter, major diameter, thread pitch, and pitch on the Crosscheck are out of specification, which may result in intraoperative malfunction.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1490-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-03-06 |
| Published | 2015-04-29 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Wright Medical Technology |
| Distribution | US |
Product
CROSSCHECK(R) Plating system, MTP NX Plate, Left, Recon, REF CCP-MPN2L. Orthopedic use.
Reason
The minor diameter, major diameter, thread pitch, and pitch on the Crosscheck are out of specification, which may result in intraoperative malfunction
Identifiers
| code_info | Lot Numbers: 3504917, 35049-17A, 35049-17A-1, 35049-18, 362791, 36279-1-1 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Other recalls by Wright Medical Technology
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FDA Device · Class II · 2026-10-07 · Wright Medical Technology - stryker Infinity Resection Adjustment Block, REF 33600030, ankle arthroplasty
FDA Device · Class II · 2024-04-10 · Wright Medical Technology - Stryker Infinity Alignment Frame Distal Sub-Assembly, Catalog #33600020, non-sterile
FDA Device · Class II · 2023-07-12 · Wright Medical Technology - stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A220RT, bone stabilization and fixation
FDA Device · Class II · 2023-05-03 · Wright Medical Technology - stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A221RT, bone stabilization and fixation
FDA Device · Class II · 2023-05-03 · Wright Medical Technology
All Wright Medical Technology recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1490-2015%22
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