Bad Fallingbostel, Germany
KAYSERBETTEN GMBH & CO. KG recalls
1 recall recorded since 2018, most recently on 4 May 2026. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)1
Terminated or completed0
Class I (FDA)1
Ongoing Class I Medical devices
- Recall started
- 4 May 2026
- Reason
- If the adjustment functions of the hand control, as instructed in the Manual, are not locked with the provided key when the patient (child) is unattended, there is an increased risk that the patient (child) or third parties (children) will operate the hand control and trap themselves or others under the bed frame or between the bed frame and the floor. This can lead to serious injuries or even death of the patient (child) or third parties (children).
- Distribution
- Distribution US Nationwide and Canada.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2212-2026
- Pediatric care bed; Product Designation: KayserBett IDA;
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.