Critical Alert
KAYSERBETTEN GMBH & CO. KG Recalls Pediatric care bed; Product Designation: KayserBett IDA
This is a Class I recall — the most serious type. There is a reasonable probability of serious health consequences or death.
Source: FDA
CriticalRecall #Z-2212-2026Medical Device
KAYSERBETTEN GMBH & CO. KG Recalls Pediatric care bed; Product Designation: KayserBett IDA
KAYSERBETTEN GMBH & CO. KG · Class I — Most Serious
Product Description
Pediatric care bed; Product Designation: KayserBett IDA;
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).
FDA Classification
Class I — Most Serious
A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Distribution
Distribution US Nationwide and Canada.
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
The FDA has classified this as a Class I recall — the most serious classification reserved for situations where there is a reasonable probability that use of, or exposure to, the product will cause serious adverse health consequences or death. KAYSERBETTEN GMBH & CO. KG initiated this recall of medical device on May 4, 2026 affecting 372 units. 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. The product was distributed in Distribution US Nationwide and Canada. Consumers who have this product should stop using it immediately and contact the recalling firm.
Sources: FDA openFDA Enforcement Database
This recall appears in: Poison & Chemical Hazards.