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DePuy Synthes Super Qa+ O C DS CP-2 *Ea
No active recall
Manufacturer: DePuy Synthes · FDA product code: JDR · Category: Staple, Fixation, Bone
Severity Snapshot
36 total reports2019-01 – 2025-05 date range5.6% physician / facility reported94.4% manufacturer reported2 SKU variants
Failure & Consequence Profiles
Top Failure Modes
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Top Patient Outcomes
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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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