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Recall Observatory FDA recall evidence

Device product

ActiveAid 922, Shower/Commode Chair

Z-0880-2023

November 30, 2022

Class II

Product summary

Firm
Altimate Medical, Inc.
Event
Event 91335
Status
Terminated
Classification
Class II
Quantity
1 unit
Official record key
device-enforcement:Z-0880-2023

Official wording

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.

Code information: Serial Number 90071504001

Distribution pattern: US Nationwide distribution in the state of Texas.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.