ASPIRON™ ACP SYSTEM NC3514VDRecalls & reported problems
CG MedTech Co.,Ltd. · Class 2 · Implant
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 08800015909877), received between Jul 18, 2018 and Jul 18, 2018 — classified as 2 injuries.
The most frequently reported specific device problem is “Unintended Movement” (2 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Unintended Movement2
Patient problems
- No Known Impact Or Consequence To Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJul 18, 2018Unintended Movement
IT WAS REPORTED THAT PATIENT WAS OPERATED WITH ANTERIOR CERVICAL PLATE SYSTEM. A SCREW IN C3 HAS BACKED OUT POSTOPERATIVELY. THERE WERE NO REPORTS OF PATIENT INJURY. THERE WAS NO REVISION SURGERY TO PATIENT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7697408 ↗InjuryJul 18, 2018Unintended Movement
IT WAS REPORTED THAT PATIENT WAS OPERATED WITH ANTERIOR CERVICAL PLATE SYSTEM. A SCREW IN C4 HAS BACKED OUT POSTOPERATIVELY. THERE WERE NO REPORTS OF PATIENT INJURY. THERE WAS NO REVISION SURGERY TO PATIENT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7697406 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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