Neurovision Medical Products Inc

FDA recalling firm · 3 enforcement events · 11 product records · 2020–2025 · CA

Neurovision Medical Products Inc has 3 FDA enforcement events on this register (11 product records) between 2020 and 2025: 3 device; the busiest year was 2020 with 1.

0% of its events are Class I; the most common class is Class II (3). 2 events are listed as ongoing; the recalling firm's address is in CA.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

Initiated	Product (first record)	Type	Class	Records	Status
19 May 2025	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…	Device	Class II	1	Ongoing
1 Jul 2024	Cobra, 3-Plate EMG ET Tube, 6.0mm, REF: LTE7003PM, not made with natural rubber latex, Rx Only, STERILEEO	Device	Class II	1	Ongoing
21 Jul 2020	Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMG ET Tube, 6.0mm REF NVTKIT-C6-5, Rx Only, Sterile, UDI: B006NVTKITC652/$$7061918A - Product Usage: For continuous EMG monitoring and status assessment of the nerves supplying the laryngeal musculature as well as providing an open airway for patient ventilation during…	Device	Class II	9	Terminated

By type and class

Device3

Class II3

Class I: 0% of this firm's events; 18% of all events on the register.

Events by year

Enforcement events for Neurovision Medical Products Inc by year initiated.

Questions and answers

How many FDA recalls has Neurovision Medical Products Inc had?

3 enforcement events (11 product records) on this register, 2020–2025: 3 device.

Are any Neurovision Medical Products Inc recalls ongoing?

2 events are listed as ongoing in the current openFDA export.

What class are Neurovision Medical Products Inc recalls?

3 Class II. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.