PlainRecalls
FDA Devices Moderate Class II Terminated

ActiveAid 922, Shower/Commode Chair

Reported: January 11, 2023 Initiated: November 30, 2022 #Z-0880-2023

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.

Details

Recalling Firm
Altimate Medical, Inc.
Units Affected
1 unit
Distribution
US Nationwide distribution in the state of Texas.
Location
Morton, MN

Frequently Asked Questions

What product was recalled?
ActiveAid 922, Shower/Commode Chair. Recalled by Altimate Medical, Inc.. Units affected: 1 unit.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on January 11, 2023. Severity: Moderate. Recall number: Z-0880-2023.