Quick Facts at a Glance
- Recall Date
- May 4, 2026
- Hazard Level
- HIGH
- Brand
- KAYSERBETTEN GMBH & CO. KG
- Geographic Scope
- 1 states
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- KAYSERBETTEN GMBH & CO. KG
- Model numbers
- Product Designation: KayserBett IDA, UDI-DI: 426038961IDAGU, Serial Number: 386, 387, 388, 389, 390, 391 +12 more
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
May 4, 2026
Reported by FDA DEVICE
June 10, 2026
RecallRadar source check
June 16, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
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 You Should Do
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact KAYSERBETTEN GMBH & CO. KG or your healthcare provider for instructions. Notification method: Letter
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Full Description
Pediatric care bed; Product Designation: KayserBett IDA;. 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).. Classification: Class I. Quantity: 372 units. Distribution: Distribution US Nationwide and Canada.
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Safety Guide
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