Midmark

MIDMARK CORPORATION · Model 9A411004 · UDI-DI 00841709113239

510(k) clearances

Adverse events (1 deaths)

Recalls

Facilities

Description

The Articulating Knee Crutch Kit (with accessory receiver) is designed to be a more ergonomic and comfortable option compared to standard stirrups. The unique ball-socket design allows for a maximum range of adjustment, designed to ensure optimum knee and leg support.

Recalls

Date	Firm	Reason
2014-11-14	TransMotion Medical Inc	The firm is finding that the stretcher chair controllers are moving the chairs involuntarily.

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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.