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.