ActiveAid 922, Shower/Commode Chair — FDA record Z-0880-2023

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Nov 30, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

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.
Classification
Class II
Recalling firm
Altimate Medical, Inc.
Quantity
1 unit
Agency-reported status
Terminated
Source record identifier
Z-0880-2023

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilitySerial Number 90071504001

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

US Nationwide distribution in the state of Texas.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Report date
Jan 11, 2023
Recall initiation date
Nov 30, 2022
Center classification date
Jan 4, 2023
Termination date
Aug 31, 2023

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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