FDA Medical Device Recalls (openFDA)
Altimate Medical, Inc.: ActiveAid 922, Shower/Commode Chair
- Recall number
- Z-0880-2023
- Recalling firm
- Altimate Medical, Inc.
- Product
- ActiveAid 922, Shower/Commode Chair
- Status
- Terminated
- Initiated
- 2022-11-30
- Posted
- 2023-01-04
- Terminated
- 2023-08-31
- 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.
- Root cause
- Component change control
- Action
- Altimate Medical notified its sole consignee by telephone on 11/30/2022 and followed with an Urgent Medical Device Recall letter on 12/06/2022. The notice stated the problem and requested the following action: "- Acknowledge receipt of this notification. Complete and return the attached Acknowledgement form. - Inform the customer not to use the chair if this has not already done. - Provide replacement chair 90071504001 under RMA000737 to AMI - Inform Altimate when the replacement chair is provided to the customer. Complete and return the attached Verification form."
- Quantity
- 1 unit
- Distribution
- US Nationwide distribution in the state of Texas.
- Lot, serial or model codes
- Serial Number 90071504001
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- INN
- Firm FEI
- 2183634
- Firm city
- Morton
- Firm state
- MN
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28