The Recall Desk
HighFDA (Devices)·Z-0880-2023·Announced 2023-01-11

Shower/Commode Chair Recalled Due to Frame Folding Defect

Altimate Medical is recalling the ActiveAid 922 Shower/Commode Chair because a manufacturing defect prevents the frame from folding properly and being secured by the frame strap in the folded position.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: This is a Class II FDA medical device recall involving a structural defect in a mobility device. The frame defect prevents proper folding and securing, creating a potential safety hazard during transport or storage. Per the severity rubric, risk-of-harm products where injury has not yet been reported are classified as High (Score 3).

Plain-English summary

Altimate Medical, Inc. is recalling the ActiveAid 922 Shower/Commode Chair (serial number 90071504001) due to a manufacturing component defect. The device was manufactured with a component that affects the foldability of the frame, preventing it from being secured by the frame strap in the folded position.

This recall affects units distributed nationwide in the state of Texas. The FDA classified this as a Class II recall.

The recalled product

Product
ActiveAid 922, Shower/Commode Chair
Manufacturer
Altimate Medical, Inc.
Category
Medical Device — Mobility Equipment
Hazard
Affected units
1

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • Serial Number 90071504001

Distribution

Distributed nationwide across the United States.

The notice also names 1 state specifically:

Related recalls

Same manufacturer · Altimate Medical, Inc.

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Same hazard · structural defect

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