ActiveAid 922 Chair (Altimate Medical) – Frame Foldability Issue (2022)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
ActiveAid 922, Shower/Commode Chair
Brand
Altimate Medical, Inc.
Lot Codes / Batch Numbers
Serial Number 90071504001
Products Sold
Serial Number 90071504001
Altimate Medical, Inc. is recalling ActiveAid 922, Shower/Commode Chair due to 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 positio. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
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."
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026