FDA Medical devices recall ·
Hummingbird Product Name: Stimulated EMG Kit with Hummingbird - Model recall
- Recall number
- Z-2100-2025
- Date
- (initiated May 19, 2025)
- Company / brand
- Neurovision Medical Products Inc
353 San Jon Rd, Ventura, CA, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 10
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
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
Why was it recalled?
Product packaging contains the wrong part number and kit contents.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
REF I-D-BMF90 & 1-D-BMF90-5, lot number: 050925219
Distribution
US distribution to CA only
States: California
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-2100-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.