GE Healthcare Recalls Discovery NM670 Pro Due to Loose Screws
GE Healthcare is recalling nine Discovery NM670 Pro units because rotor bearing screws were found loose on the detector.
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: The recall is classified as FDA Class II, which typically indicates a moderate risk. The specific defect (loose screws) is a mechanical issue that may lead to device malfunction, but no injuries or illnesses are reported in the source text.
Plain-English summary
GE Healthcare, LLC is recalling nine units of the Discovery NM670 Pro (Model # H3100XB) medical device. The recall was initiated because rotor bearing screws were found loose on the detector.
The affected units are distributed across 29 states in the United States and 28 countries internationally. Specific serial numbers and system IDs for the nine units are listed in the official recall documentation.
Healthcare facilities should contact GE Healthcare for instructions on how to address the loose screws. The source text does not specify a remediation method or a deadline for the recall.
The recalled product
- Product
- Discovery NM670 Pro Model # H3100XB
- Manufacturer
- GE Healthcare, LLC
- Hazard
- Affected units
- 9
Distribution
Part of a larger recall action
This product is one of 8 recalled by GE Healthcare, LLC under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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