Device recall
Z-1436-2026: MRI LED Mobile Exam Light Battery REF SL-111 This non-magnetic UL and CE…
FDA device recall · Class II · MRIMed Inc.
Key facts
| Recall number (Z-number) | Z-1436-2026 |
|---|---|
| Recall event | 98127 |
| Product | MRI LED Mobile Exam Light Battery REF SL-111 This non-magnetic UL and CE approved battery is used in conjunction with SL-110, Mobile Exam Light |
| Product code | KZF |
| Recalling firm | MRIMed Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3009560891 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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