Home/Recalls/FDA-Z-2212-2026
FDA DevicesClass I

Pediatric care bed; Product Designation: KayserBett IDA;

Published: June 10, 2026Recall ID: Z-2212-2026Category: devicesCountry: US
US
Medical DeviceFDA DevicesUSUS

Pediatric care bed; Product Designation: KayserBett IDA;

Recalling Firm: KAYSERBETTEN GMBH & CO. KG

Reason for Recall / 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).

Product Description & Identification

Pediatric care bed; Product Designation: KayserBett IDA;

Affected Products

Pediatric care bed; Product Designation: KayserBett IDA;

Additional Source Details

FieldValue
CityBad Fallingbostel
Event id98820
Address 1Rieper Str. 12
Code infoProduct Designation: KayserBett IDA; UDI-DI: 426038961IDAGU; Serial Number: 386, 387, 388, 389, 390, 391, 392, 635, 636, 637, 638, 639, 641, 642, 643, 644, 645, 646, 647, 1072, 1073, 1074, 1075, 1076, 1077, 1078, 1079, 1080, 1081, 1082, 1083, 1085, 1086, 1087, 1088, 1089, 1090, 1110, 1111, 1446, 1447, 1448, 1449, 1648, 1649, 1950, 1975, 1976, 1982, 1983, 1998, 2001, 2003, 2004, 2337, 2338, 2339, 2340, 2341, 2342, 2343, 2344, 2345, 2396, 2763, 2764, 2765, 2766, 2767, 2770, 2771, 2772, 2773, 2774, 3087, 3088, 3089, 3090, 3091, 3092, 3167, 3299, 3300, 3301, 3302, 3303, 3304, 3305, 3306, 3309, 3310, 3311, 3312, 3313, 3314, 3740, 3741, 3760, 4223, 4232, 4233, 4234, 4235, 4236, 4237, 4239, 4240, 4242, 4243, 4244, 4245, 4246, 4247, 4248, 4249, 4250, 4567, 4568, 4569, 4570, 4571, 4572, 4573, 4574, 4575, 4576, 4577, 4578, 4579, 4580, 4581, 4582, 4583, 4584, 4986, 5238, 5254, 5255, 5256, 5257, 5258, 5259, 5637, 5919, 5920, 5921, 5922, 5923, 5924, 5925, 5926, 5937, 5938, 5939, 5940, 5948, 6332, 6... [TRUNCATED]
Postal codeN/A
Report date20260610
Product typeDevices
Product quantity372 units
Reason for recallIf 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).
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260504
Initial firm notificationLetter
Center classification date20260604

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Overview

  • Recalling FirmKAYSERBETTEN GMBH & CO. KG
  • StatusOngoing
  • Risk LevelClass I
  • DistributionDistribution US Nationwide and Canada.
Recall Hazard Severity
High Alert (Class I)
Official Agency Alert

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🚨 SAFETY ALERT: KAYSERBETTEN GMBH & CO. KG - Pediatric care bed; Product Designation: KayserBett IDA;

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https://therecallfile.com/recalls/pediatric-care-bed-product-designation-kayserbett-ida/FDA-Z-2212-2026
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