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ActiveAid 922, Shower/Commode Chair

FDA Recall #Z-0880-2023 — Class II — November 30, 2022

Recall #Z-0880-2023 Date: November 30, 2022 Classification: Class II Status: Terminated

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.

Recalling Firm

Altimate Medical, Inc. — Morton, MN

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Devices

Product Quantity

1 unit

Distribution

US Nationwide distribution in the state of Texas.

Code Information

Serial Number 90071504001

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated

What Should You Do?

Stop using this medical device immediately and consult your healthcare provider. Contact the recalling firm for instructions on return or replacement. If you experienced an adverse event, inform your doctor.

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