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Collect NO Qas Spine Anterior Stabilis
No active recall
FDA product code: KWQ · Category: Appliance, Fixation, Spinal Intervertebral Body
Severity Snapshot
267 total reports2019-08 – 2025-06 date range88.2% physician / facility reported11.8% manufacturer reported1 SKU variants
Reporting Trend
Annual Reporting Volume
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Note: the 2018 Voluntary Malfunction Summary Reporting expansion means volume increases may reflect surveillance changes, not increased device risk.
Reported Events
Submitted to FDA MAUDE by physicians, hospitals, manufacturers, and patients.
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