Brand Name: Hummingbird Product Name: Stimulated EMG Kit with… — Class II medical device recall Z-2100-2025
Ongoing recall by Neurovision Medical Products Inc, reported 2025-07-16, distributed in CA. Product packaging contains the wrong part number and kit contents.
| Recall number | Z-2100-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Neurovision Medical Products Inc, Ventura, CA, United States |
| Recall initiated | 2025-05-19 |
| Classified | 2025-07-09 |
| Reported by FDA | 2025-07-16 |
| Distributed | CA |
| Quantity | 10 |
| Lot numbers | 050925219, I-D-BMF90-5 |
| Model numbers | 1-D-BMF90-5, I-D-BMF90 |
| Expiration dates | 2028-11-30 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2100-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.