# FDA recall Z-2100-2025

> **Neurovision Medical Products Inc** · Class II · device recall initiated 2025-05-19.

## 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 Hummingbird - Box of 5 Kits - Each Kit Includes:  1 Single-Use Bipolar Minifork Stimuation Probe, 90mm, and 1 Green Ground Needle

## Reason for recall

Product packaging contains the wrong part number and kit contents.

## Distribution

US distribution to CA only

## Key facts

- **Recall number:** Z-2100-2025
- **Recalling firm:** Neurovision Medical Products Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-05-19
- **Report date:** 2025-07-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Ventura, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2100-2025

## Citation

> AI Analytics. FDA recall Z-2100-2025. Retrieved 2026-09-14 from https://api.ai-analytics.org/recall/Z-2100-2025. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*