Class I — KAYSERBETTEN GMBH & CO. KG
| Recalling firm | Kayserbetten GmbH & Co. KG |
|---|---|
| Registered facility | Kayserbetten GmbH & Co. KG (the firm's only registered facility) |
| Classification | Class I |
| Status | Ongoing |
| 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). |
| Product | Pediatric care bed; Product Designation: KayserBett IDA; |
| Quantity | 372 units |
| Distribution | Distribution US Nationwide and Canada. |
| Initiated | 2026-05-04 |
| Classified | 2026-06-04 |
| Recall number | Z-2212-2026 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class I recall — KAYSERBETTEN GMBH & CO. KG (Z-2212-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/98820/
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