Neurovision Medical Products Inc is recalling approximately 10 units of Hummingbird Stimulated EMG Kits because the packaging contains the wrong part numbers and incorrect kit contents. The recall affects kits with model numbers REF I-D-BMF90 and 1-D-BMF90-5 under lot number 050925219. Because the kits may contain incorrect medical components, healthcare providers should immediately stop using these specific lots to avoid using the wrong tools during clinical procedures.
The packaging errors may result in clinicians using the incorrect medical instruments or identifying parts by the wrong number, which could lead to procedural delays or complications during electromyography (EMG) testing.
REF 1-D-BMF90-5 is a Box of 5 Kits.
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · Raw API Response
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