Stimulated EMG Kit with Hummingbird recalled for incorrect packaging and part number
Neurovision Medical Products recalled the Hummingbird Stimulated EMG Kit (model I-D-BMF90) due to packaging that lists wrong part numbers and kit contents. Affected lot 050925219 was distributed to California.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: FDA Class II recall involving packaging and labeling errors with no reported injuries or illnesses. The hazard is documentation confusion rather than direct patient risk, making it a moderate-severity administrative issue.
Plain-English summary
Neurovision Medical Products Inc. is recalling the Hummingbird Stimulated EMG Kit (Model REF I-D-BMF90 and REF I-D-BMF90-5) due to incorrect part numbers and kit contents information printed on the product packaging. The packaging does not accurately reflect the actual contents of the kit, which includes one Single-Use Bipolar Minifork Stimulation Probe (90mm) and one Green Ground Needle.
This packaging mislabeling could lead to confusion about what is contained in the kit and may result in improper use or incorrect documentation. The recall affects lot number 050925219 (expiration date 2028-11-30), with approximately 10 units distributed to California.
Consumers who have received this product should verify the actual kit contents against the packaging labels and contact Neurovision Medical Products Inc. for further instructions or replacement units.
The recalled product
- 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 Stim
- Manufacturer
- Neurovision Medical Products Inc
- Hazard
- packaging-mislabeling
- wrong-part-number
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- REF I-D-BMF90 & 1-D-BMF90-5
- lot number: 050925219
Distribution
Distributed in 1 state:
- CA
Related recalls
Same category
- SevereMedline Spinal Trays Recalled Due to Quality and Efficacy Concerns
FDA (Devices) · 2026-06-03
- SevereMedline Spinal Block Kits Recalled for Data Integrity and Efficacy Issues
FDA (Devices) · 2026-06-03
- HighGE APEXPRO and CARESCAPE Telemetry Systems Risk Loss of Patient Monitoring
FDA (Devices) · 2026-06-03
- CriticalMedline spinal anesthetic kits recalled for quality and efficacy concerns
FDA (Devices) · 2026-06-03
- SevereMedline spinal anesthesia kits recalled for bupivacaine quality issues
FDA (Devices) · 2026-06-03