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DePuy Synthes Gii Qa+ W #2 Orthocord
No active recall
Manufacturer: DePuy Synthes · FDA product code: JDR · Category: Staple, Fixation, Bone
Severity Snapshot
27 total reports2014-08 – 2023-08 date range22.2% physician / facility reported77.8% 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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