Recall Z-0880-2023— Altimate Medical, Inc.

Class II · Terminated

Class II FDA medical device recall by Altimate Medical, Inc., initiated 2022-11-30, terminated 2023-08-31. FDA's recall record names no specific 510(k) clearance for this event. Product: ActiveAid 922, Shower/Commode Chair. Reason: Device manufactured with a component with affects the foldability of the frame, not allowing it to be secured by the frame strap in the folded position..

Recalling firm
Altimate Medical, Inc.
Classification
Class II
Status
Terminated
Initiated
2022-11-30
Terminated
2023-08-31
Firm location
Morton, MN, United States

Product description

ActiveAid 922, Shower/Commode Chair

Reason for recall

Device manufactured with a component with affects the foldability of the frame, not allowing it to be secured by the frame strap in the folded position.

Data sourced from openFDA. This site is unofficial and independent of the FDA.