---
title: "Brand Name: Hummingbird Product Name: Stimulated EMG Kit with Hummingbird - M... — FDA record Z-2100-2025 | Is It on Recall"
description: "Product packaging contains the wrong part number and kit contents."
url: https://isitonrecall.com/recall/fda-device-z-2100-2025-brand-name-hummingbird-product-name-stimulated-emg-kit-with-hummingbird-model-catalog-number-ref-i-d/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Brand Name: Hummingbird Product Name: Stimulated EMG Kit with Hummingbird - Model/Catalog Number: REF I-D-BMF90, 1 Si... — FDA record Z-2100-2025

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date May 19, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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**: Product packaging contains the wrong part number and kit contents.
- **Classification**: Class II
- **Recalling firm**: Neurovision Medical Products Inc
- **Quantity**: 10
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2100-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2100-2025%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | REF I-D-BMF90 & 1-D-BMF90-5, lot number: 050925219 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US distribution to CA only

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [California](https://isitonrecall.com/state/california/)

## Dates in the source

- **Report date**: Jul 16, 2025
- **Recall initiation date**: May 19, 2025
- **Center classification date**: Jul 9, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2100-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Neurovision Medical Products Inc records](https://isitonrecall.com/brand/neurovision-medical-products-inc/)