Recall Z-2100-2025— Neurovision Medical Products Inc
Class II · Ongoing
Class II FDA medical device recall by Neurovision Medical Products Inc, initiated 2025-05-19. FDA's recall record names no specific 510(k) clearance for this event. 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..
- Recalling firm
- Neurovision Medical Products Inc
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2025-05-19
- Firm location
- Ventura, CA, United States
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.