Hummingbird stimulated EMG kit packaging shows the wrong part number
The Hummingbird Stimulated EMG Kit is being recalled because the product packaging contains the wrong part number and kit contents. 10 units are affected.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
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 for a packaging and part number discrepancy with no device defect or clinical consequence stated in the source.
Plain-English summary
The Stimulated EMG Kit with Hummingbird, REF I-D-BMF90, containing one single-use bipolar minifork stimulation probe, 90 mm, and one green ground needle, together with REF 1-D-BMF90-5, is being recalled. The action covers 10 units from lot 050925219.
The stated reason is that the product packaging contains the wrong part number and kit contents. The FDA classified the action as Class II. The source does not describe a resulting clinical consequence.
Distribution was in California only. The kits are supplied to healthcare facilities rather than sold to consumers.
Facilities should identify affected stock using the REF numbers and lot number above and follow the instructions issued by the manufacturer.
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…
- Manufacturer
- Neurovision Medical Products Inc
- Affected units
- 10
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:
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