Device recall
Z-2212-2026: Pediatric care bed; Product Designation: KayserBett IDA;
FDA device recall · Class I · KAYSERBETTEN GMBH & CO. KG
Key facts
| Recall number (Z-number) | Z-2212-2026 |
|---|---|
| Recall event | 98820 |
| Product | Pediatric care bed; Product Designation: KayserBett IDA; |
| Product code | FNL |
| Recalling firm | KAYSERBETTEN GMBH & CO. KG |
| Recall class | Class I |
| Status | Open, Classified |
| FEI number | 3006795806 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database