CLASS II ONGOING Device recall · Reported 16 Jul 2025 · FDA Enforcement Report
Stimulated EMG Kit with Hummingbird recalled
Neurovision Medical Products is recalling Stimulated EMG Kit with Hummingbird, distributed in California. The recall was initiated on 19 May 2025 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-2100-2025
- FDA event ID
- 96956
- Recalling firm
- Neurovision Medical Products, Ventura, CA
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 19 May 2025
- FDA classified
- 9 Jul 2025
- Reported
- 16 Jul 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Packaging Defects
- Device type
- Syringes & Needles
Timeline
| 19 May 2025 | Recall initiated by company | |
| 9 Jul 2025 | Classified by FDA | +51 days |
| 16 Jul 2025 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Product packaging contains the wrong part number and kit contents.
Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.
Product as listed by the FDA
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
Where it was distributed
US distribution to CA only
Questions about this recall
Is Stimulated EMG Kit with Hummingbird recalled?
Yes. Neurovision Medical Products recalled Stimulated EMG Kit with Hummingbird on 19 May 2025. The recall is Class II and its status is Ongoing. Recall number Z-2100-2025.
Why was it recalled?
Product packaging contains the wrong part number and kit contents.
Which lots are affected?
REF I-D-BMF90 & 1-D-BMF90-5, lot number: 050925219
Where was it sold?
US distribution to CA only
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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