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MotoBAND

CROSSROADS EXTREMITY SYSTEMS · Model Implant, MotoBAND CP, MTP Plate, Right - Sterile · UDI-DI 00815432022786

HWC HRS Prescription

510(k) clearances

59,207

Adverse events (76 deaths)

389

Recalls

656

Facilities

Description

The MotoBAND™ CP Implant System is a bone plating system indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion and reconstruction of small bones of the hand, feet, wrist, ankles, fingers and toes. It consist of plates and screws. Some plates in this system are compatible with the MotoCLIP Implant System.

Recalls

Date	Firm	Reason
2026-09-09	In2bones USA, LLC	Due to labeling error, bone screws specified as fully threaded, are actually partially threaded screws.
2026-04-24	Medartis AG	The cannulation of the CCS screw is not centered.
2026-01-23	I.T.S. GmbH	Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
2026-01-23	I.T.S. GmbH	Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
2026-01-09	Medartis AG	Mix up between specified lots of 2.5mm and 2.8mm outer diameter screws.
2026-01-09	Medartis AG	Mix up between specified lots of 2.5mm and 2.8mm outer diameter screws.
2025-11-24	Smith & Nephew, Inc.	Removal of affected lot of screws due to labeling error.
2024-04-12	Medartis Inc.	Screw is 16mm long instead of 22mm long.
2024-03-20	Zimmer, Inc.	Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user sinc
2024-03-20	Zimmer, Inc.	Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user sinc

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.