Pediatric care bed; Product Designation: KayserBett IDA;
KAYSERBETTEN GMBH & CO. KG
The hazard
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). FDA Class I recall.
The remedy
Follow FDA guidance
About this recall
Pediatric care bed; Product Designation: KayserBett IDA;
Affected identifiers
Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.
Model Product Designation: KayserBett IDAModel UDI-DI: 426038961IDAGUModel Serial Number: 386Model 387Model 388Model 389Model 390Model 391Model 392Model 635Model 636Model 637Model 638Model 639Model 641Model 642Model 643Model 644Model 645Model 646Model 647Model 1072Model 1073Model 1074Model 1075Would you have heard about this one?
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Start monitoring freeSourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.