NuVasive 6900101Recalls & reported problems
Nuvasive, Inc. · Universal Inserter, CoRoent XL · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887517382351), received between Apr 2, 2017 and Apr 2, 2017 — classified as 1 injury.
The most frequently reported specific device problem is “Device Slipped” (1 report).
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
- Device Slipped1
- Unintended Movement1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 2, 2017Device Slipped; Unintended Movement; Device Slipped; Unintended Movement
ON (B)(6) 2017 A FEMALE PATIENT (B)(6) UNDERWENT A PROCEDURE ON L3 TO L4 LEVELS. IN THE INITIAL SURGERY THE IMPLANT WAS PLACED WITHOUT ISSUE BUT THE SURGEON BELIEVED HE MAY HAVE BREACHED THE PERITONEUM. AS A RESULT HE OPTED TO REMOVE AND REPLACE THE IMPLANT DURING A REVISION SURGERY ON (B)(6) 2017. THE CAGE WAS REMOVED AND REPLACED WITHOUT FURTHER INCIDENT TO THE PATIENT.
Patient problems: Foreign Body In Patient
MAUDE report 6452427 ↗
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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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