PCM 7680359Recalls & reported problems
Nuvasive, Inc. · PCM V Disc, 5.9mm Medium (US) · Class 3 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887517601155), received between Oct 11, 2017 and Oct 11, 2017 — classified as 1 malfunction.
The most frequently reported specific device problem is “Unintended Movement” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Unintended Movement1
Patient problems
- Failure of Implant1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 11, 2017Unintended Movement; Unintended Movement
ON (B)(6) 2017 A PATIENT UNDERWENT A POROUS COATED MOTION IMPLANT PLACEMENT PROCEDURE AT C5-C6 LEVELS WITH NO REPORTED ISSUES. POST-OPERATIVELY THE PATIENT SUFFERED A FALL DURING WHICH THE INFERIOR PLATE MIGRATED ANTERIORLY. ON (B)(6) 2017 A REVISION ANTERIOR CERVICAL DISCECTOMY FUSION PROCEDURE TOOK PLACE WHERE THE POROUS COATED MOTION IMPLANT WAS REPLACED WITH ANOTHER MANUFACTURER'S DEVICE. NO PATIENT INJURY REPORTED.
Patient problems: Failure of Implant
MAUDE report 6940718 ↗
Other PROSTHESIS, INTERVERTEBRAL DISC devices
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- Simplify® Cervical Artificial DiscNuvasive, Inc. · Prosthesis, Intervertebral Disc1 recall12 reports
- Prodisc C 09.820.055SCentinel Spine, LLC · Prosthesis, Intervertebral Disc1 recall9 reports
- Simplify® Cervical Artificial DiscNuvasive, Inc. · Prosthesis, Intervertebral Disc1 recall4 reports
- Prodisc C SK PDSXL5Centinel Spine, LLC · Prosthesis, Intervertebral Disc1 recall3 reports
- Simplify® Cervical Artificial DiscNuvasive, Inc. · Prosthesis, Intervertebral Disc1 recall3 reports
- Simplify® Cervical Artificial DiscNuvasive, Inc. · Prosthesis, Intervertebral Disc1 recall3 reports
- Simplify® Cervical Artificial DiscNuvasive, Inc. · Prosthesis, Intervertebral Disc1 recall3 reports
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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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