# FDA recall Z-2212-2026

> **KAYSERBETTEN GMBH & CO. KG** · Class I · device recall initiated 2026-05-04.

## Product

Pediatric care bed;  Product Designation: KayserBett IDA;

## Reason for recall

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.

## Key facts

- **Recall number:** Z-2212-2026
- **Recalling firm:** KAYSERBETTEN GMBH & CO. KG
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-05-04
- **Report date:** 2026-06-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Bad Fallingbostel, Germany

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2212-2026

## Citation

> MORVS. FDA recall Z-2212-2026. Retrieved 2026-10-19 from https://api.morvs.ai/recall/Z-2212-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*