FDA recall Z-0880-2023

Altimate Medical, Inc. · Class II · device

Product

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.

Distribution

US Nationwide distribution in the state of Texas.

Key facts

Status: Terminated
Initiation date: 2022-11-30
Report date: 2023-01-11
Termination date: 2023-08-31
Voluntary/Mandated: Voluntary: Firm initiated
Location: Morton, MN, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0880-2023