Severity
Moderate
ModerateClass IIOngoing
FDA Devices recall · Reported July 16, 2025
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
Product packaging contains the wrong part number and kit contents.
Neurovision Medical Products Inc recalled Brand Name: Hummingbird Product Name: Stimulated EMG Kit with Hummingbird - Model/Cata… - a moderate-severity action.
Brand Name: Hummingbird Product Name: Stimulated EMG Kit with Hummingbird - Model/Cata… was recalled by Neurovision Medical Products Inc in July 16, 2025. Reason: Product packaging contains the wrong part number and kit contents.. Check the official notice for the remedy. Verify recall #Z-2100-2025 with the FDA Devices before acting.
The recall
Neurovision Medical Products Inc issued this moderate-severity FDA Devices recall-Product packaging contains the wrong part number and kit contents..
- Moderate
- severity level
- 10 units
- affected scope
- Class II
- classification
- July 16, 2025
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2100-2025 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-2100-2025) was formally reported on July 16, 2025, with the manufacturer initiating the action on May 19, 2025. It is classified under Moderate severity (Class II), with a current status of Ongoing. Neurovision Medical Products Inc is listed as the recalling firm, operating out of Ventura, CA. Federal records list the affected scope as 10.
The documented reason for this recall is: Product packaging contains the wrong part number and kit contents. Distribution data in the federal record shows the product reached: US distribution to CA only. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
10
Related Recalls
6
3 from same agency
Product description
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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | Z-2100-2025 |
| Date reported | July 16, 2025 |
| Date initiated | May 19, 2025 |
| Recalling firm | Neurovision Medical Products Inc |
| Firm location | Ventura, CA |
| Affected scope | 10 |
| Distribution | US distribution to CA only |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-2100-2025) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Neurovision Medical Products Inc. Units affected: 10.
Why was this product recalled? ▼
Product packaging contains the wrong part number and kit contents.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 16, 2025. Severity: Moderate. Recall number: Z-2100-2025.
Where was the recalled product distributed? ▼
Distribution: US distribution to CA only.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-2100-2025) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported July 16, 2025. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.