Z-2212-2026Class I

Pediatric care bed; Product Designation: KayserBett IDA

Name: Z-2212-2026 Pediatric care bed; Product Designation: KayserBett IDA
Creator: Kayserbetten Gmbh & Co. Kg
Published: 2026-05-04
License: https://open.fda.gov/license/

Kayserbetten GmbH & Co. KG / initiated 2026-05-04 / Open, Classified / root cause: design

FDA source

KAYSERBETTEN GMBH & CO. KG began a recall of Pediatric care bed; Product Designation: KayserBett IDA on 2026-05-04. FDA classified it as Class I and gives the reason as "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...". As of 2026-09-10, the recall status on record is Open, Classified, and MDM tags the root cause as design.

Recall record

Recall number: Z-2212-2026
Classification: Class I
Status: Open, Classified
Initiated: 2026-05-04
Posted: 2026-06-04
Recalling firm: Kayserbetten GmbH & Co. KG
Product: Pediatric care bed; Product Designation: KayserBett IDA;
Product code: FNL Bed, Ac-Powered Adjustable Hospital
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).
Root cause tag: design
FDA root cause: Device Design
Action: On May 4, 2026 Urgent Field Safety Notice letters were sent to customers. Actions to be taken: Please inform all users and operators of a KayserBett IDA that by implementing the following safety measures, the above-mentioned risk to patients or third parties can be eliminated during further use of the product. If the patient is unattended, " the sleeping platform must be lowered to its lowest position. " the adjustment functions on the hand control must be locked using a key. " the doors must be closed. KayserBetten is implementing a corrective action to replace the hand control on all affected KayserBett IDA beds in the U.S. field with a modified hand control featuring an automatic locking function (Auto-Lock). With the new hand control, the adjustment functions lock automatically after each use, eliminating the dependence on the caregiver manually locking the hand control with a key. The hand control replacement will be performed by an authorized service technician at no cost to the customer. Your U.S. distributor, Mobility Unlimited Inc. (DBA KayserBetten US), will contact you to schedule the replacement. Please ensure in your organization that all users of the above-mentioned product and other persons to be informed are aware of this Field Safety Notice. If you have supplied the products to third parties, please forward a copy of this information or inform the contact person listed below. Please keep this information at least until the hand control replacement has been completed.
Quantity in commerce: 372 units
Distribution: Distribution US Nationwide and Canada.
Product codes and lots: Product 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, 6338, 6339, 6340, 6341, 6342, 6343, 6344, 6345, 6346, 6347, 6351, 6355, 6795, 6796, 7176, 7177, 7178, 7179, 7180, 7181, 7182, 7183, 7184, 7185, 7186, 7187, 7188, 7189, 7190, 7191, 7192, 7193, 7194, 7195, 7617, 7618, 7619, 7620, 7621, 7622, 7623, 8242, 8243, 8244, 8245, 8588, 8589, 8590, 8591, 8592, 8593, 8594, 8595, 8596, 8597, 8598, 8599, 8600, 8601, 8602, 8603, 8608, 8609, 8691, 8704, 8912, 8921, 8922, 8923, 8924, 8925, 8926, 8927, 8928, 8929, 8930, 9725, 9726, 9727, 10350, 10351, 10352, 10819, 10820, 10821, 10822, 10823, 10824, 10825, 11186, 11367, 11368, 11369, 11370, 11371, 11372, 11797, 11798, 11799, 11800, 11801, 11802, 11803, 11804, 11805, 11806, 11807, 11808, 12247, 12248, 12249, 12250, 12251, 12252, 12253, 12254, 12255, 12256, 12257, 12397, 12398, 12399, 12782, 12783, 12963, 12964, 12965, 12966, 12967, 12968, 12969, 12970, 12971, 12972, 13486, 13487, 13488, 13489, 13490, 13491, 13492, 13493, 13494, 13495, 13496, 13497, 13912, 13913, 13914, 13915, 13916, 13917, 13918, 14942, 14944, 14952, 14953, 15912, 15913, 15914, 16403, 16404, 16405, 16406, 16407, 16408, 16409, 16410, 16411, 16984, 16985, 16986, 16987, 16988, 16989, 16990, 16991, 16992, 16993, 16994, 17577, 17578, 17579, 17580, 17581, 17582, 17583, 17584, 17585, 17586, 17587, 18494, 19112, 19113, 19114, 20151, 20152, 20153, 20154, 20155, 20156, 20157, 20158, 20963, 20964, 20965, 20966, 20967, 20968, 20969, 20970, 20972, 21192, 21193, 21194;

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-2212-2026
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-2212-2026	Class I	Ongoing	Voluntary: Firm initiated	2026-06-10	2026-06-04

Product code FNL

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)