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
FDA Recall Z-2100-2025 · Posted 2025-07-09
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Recalling FirmNeurovision Medical Products Inc
Recall StatusOpen, Classified
Product CodeETN
Date Initiated2025-05-19
Product Quantity10
Reason for Recall
Product packaging contains the wrong part number and kit contents.
Firm Action
On May 20, 2025, Neurovision Medical Products (NMP) sent consignees an email notifying them of the recall. On June 10, 2025, NMP followed up with "Urgent Medical Device Recall Notice" dated May 27, 2025, via US postal mail. Neurovision asked consignees to take the following actions:
1. Review your inventory for affected lots.
2. Quarantine product.
3. Cease distribution and use of any affected product.
4. Pass this notice on to all who need to be aware within your organization and/or to any organization where the potentially affected product has been transferred or distributed.
5. Complete and return the enclosed response form as soon as possible via email: [email protected] or Fax to: (877) 330-1727.
6. NMP Customer Service will respond with a return authorization (RMA) number and return shipping label for any remaining stock.
7. If you have distributed this product to another location or entity, notify them of this product recall (include a copy of this notice), and contact NMP Customer Service for return authorization (RMA).
If you have any questions, contact NMP Customer service at (866) 815-6999. NMP Days/Hours Available: Monday through Friday, 8am-4pm (Pacific) and
Website: neurovisionmedical.com
Root Cause
Process control
Distribution Pattern
US distribution to CA only
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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