Medical Device Recall: Pediatric care bed; Product Designation: KayserBett IDA;
KAYSERBETTEN GMBH & CO. KG · May 4, 2026
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.
States Affected
NATIONWIDE
Quantity Affected
372 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2212-2026
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.