KayserBett IDA Pediatric Care Bed Recall
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
KAYSERBETTEN GMBH & CO. KG is recalling 372 KayserBett IDA pediatric care beds distributed nationwide in the US and Canada due to entrapment risk.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on July 10, 2026 and geographically references United States and Canada. Its severity classification of "high" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, medical-devices.
What Happened
KAYSERBETTEN GMBH & CO. KG initiated a voluntary Class I recall because if the adjustment functions of the hand control 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.
Which Products Are Affected
The recall involves the Pediatric care bed with Product Designation: KayserBett IDA. UDI-DI: 426038961IDAGU. A total of 372 units are affected, identified by the listed serial numbers. Distribution was US Nationwide and Canada.
What You Should Do
Consumers should follow the locking instructions in the manual using the provided key when the patient is unattended.
Why This Matters
The hazard poses a risk of serious injury or death from entrapment.
Source
FDA recall number Z-2212-2026 (event ID 98820). https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?ID=98820
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,085 characters here).
Similar severity timing
Same severity (high) notices issued closest in time to July 10, 2026.
Frequently Asked Questions
Common questions about this FDA recall.