Official recall record

Pediatric care bed; Product Designation: KayserBett IDA;

US FDA — Medical Devices · 2026-05-04 · GermanyClass I

Issuing authority: US FDA — Medical Devices
Recall initiated by firm: 2026-05-04
Country of alert: Germany
Alert level: Class I
Alert type: recall
Brand on record: KAYSERBETTEN GMBH & CO. KG

What the authority reported

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).

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-09-16.

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