Device recall
Z-2100-2025: Brand Name: Hummingbird Product Name: Stimulated EMG Kit with Hummingbird…
FDA device recall · Class II · Neurovision Medical Products Inc
Key facts
| Recall number (Z-number) | Z-2100-2025 |
|---|---|
| Recall event | 96956 |
| Product | Brand Name: Hummingbird Product Name: Stimulated EMG Kit with Hummingbird - Model/Catalog Number: REF I-D-BMF90, 1 Single-Use Bipolar Minifork Stimulation Probe, 90mm, and 1 Green Ground Needle ; REF 1-D-BMF90-5, lot number 050925219, expiration 2028-11-30 I-D-BMF90-5 Stimulated EMG Kit with… |
| Product code | ETN |
| Recalling firm | Neurovision Medical Products Inc |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 1930870 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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