FDA Device recall Z-0522-2014

KayserBetten model IDA beds Product Usage: BED, AC-POWERED ADJUSTABLE HOSPITAL

• FDA Device
• Class II
• terminated
• Published 2013-12-25

On 2013-12-25 the FDA classified a Class II recall of KayserBetten model IDA beds Product Usage: BED, AC-POWERED ADJUSTABLE HOSPITAL by Mobility Unlimited, citing some joints on the doors of a limited number of IDA beds may loosen or separate over time which can cause the doors to drop outward and cause injury.

Read the official FDA Device notice

Product

KayserBetten model IDA beds Product Usage: BED, AC-POWERED ADJUSTABLE HOSPITAL

Reason

Some joints on the doors of a limited number of IDA beds may loosen or separate over time which can cause the doors to drop outward and cause injury.

Identifiers

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0522-2014%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.