Drug recall
Pediatric care bed; Product Designation: KayserBett IDA;
FDA recall event 98820 · Class I · KAYSERBETTEN GMBH & CO. KG
Key facts
| Event ID | 98820 |
|---|---|
| Recall numbers | Z-2212-2026 |
| Recalling firm | KAYSERBETTEN GMBH & CO. KG |
| Product type | Devices |
| Products | Pediatric care bed; Product Designation: KayserBett IDA; |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| 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… |
| Initiation date | May 4, 2026 |
| Report date | Jun 10, 2026 |
| City | Bad Fallingbostel |
| Country | Germany |
| FEI number | 3006795806 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: