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KALIX II

NEWDEAL · Model 141009ND · UDI-DI 10381780048152

HWC Prescription
10
510(k) clearances
58,942
Adverse events (75 deaths)
388
Recalls
657
Facilities

Description

The KALIX II Flat Foot implant is a combination of three sterile components. Two of them are made from Titanium alloy, and the outer sleeve is made from Ultra High Molecular Weight Polyethylene. The implant is indicated for use in the treatment of the hyperpronated foot and stabilization of the subtalar joint. It is designed to block forward, downward and medial displacement of the talus, thus allowing normal subtalar joint motion but blocking excessive pronation and the resulting sequela. Available in different sizes.

Recalls

DateFirmReason
2026-04-24Medartis AGThe cannulation of the CCS screw is not centered.
2026-01-23I.T.S. GmbHUpdated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
2026-01-23I.T.S. GmbHUpdated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
2026-01-09Medartis AGMix up between specified lots of 2.5mm and 2.8mm outer diameter screws.
2026-01-09Medartis AGMix up between specified lots of 2.5mm and 2.8mm outer diameter screws.
2025-11-24Smith & Nephew, Inc.Removal of affected lot of screws due to labeling error.
2024-04-12Medartis Inc.Screw is 16mm long instead of 22mm long.
2024-03-20Zimmer, 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
2024-03-20Zimmer, 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
2024-03-20Zimmer, 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.