Medical Depot Inc.

3 FDA enforcement actions

3 Total Recalls

1 Class I

2 Class II

0 Class III

Firm Details

Product Types: device
States: NY

All Recalls

Class I: Dangerous 04/11/2025 device

Potential for DC Power Supply housing to become hot to the touch and deform the plastic housing.
Class II: Risk 06/14/2024 device

The tiller separates from the base/front caster assembly. If the knee walker fails, a user may fall and sustain an injury
Class II: Risk 06/14/2024 device

The tiller separates from the base/front caster assembly. If the knee walker fails, a user may fall and sustain an injury

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.