Mobi-C MB3777Recalls & reported problems
LDR Spine Usa, Inc. · MOBI-C IMPLANT M « STANDARD » 17x17 H7 US · Class 3 · Implant
Data updated Oct 13, 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 03662663002035), received between May 20, 2019 and May 20, 2019 — classified as 1 injury.
The most frequently reported specific device problem is “Misassembled” (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
- Misassembled1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 20, 2019Misassembled; Misassembled
MOBI-C P&F US: DISASSEMBLED AFTER REPOSITIONING. DURING A 2 LEVELS MOBI-C SURGERY FOR C4-5 AND C6-7, IT WAS REPORTED BY SALES REPRESENTATIVE THAT THE SURGEON IMPLANTED THE MOBIC IMPLANT UNDER DISTRACTION, AND DETERMINED HE NEEDED TO REPOSITION THE IMPLANT FOR PROPER MIDLINE PLACEMENT. WHEN HE PULLED THE IMPLANT BACK, THE LOWER PLATE CAME OFF. A NEW IMPLANT WAS OPENED TO SAVE TIME. THE PARALLEL DISTRACTOR WAS USED ALONG WITH THE MOBIC CASPAR RETRACTOR. PROPER CASPAR PIN PLACEMENT OCCURRED. THE IMPLANT THAT WAS REOPENED WAS THE SAME SIZE AS THE ONE REMOVED. NO ADDITIONAL ENDPLATE PREPARATION WAS NEEDED. THE PATIENT WAS HEALTH AFTER THE SURGERY, AND HAS NOT BEEN BACK SINCE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8622923 ↗
Other Prosthesis, Intervertebral Disc devices
- Prodisc C SK PDSM5Centinel Spine, LLC · Prosthesis, Intervertebral Disc2 recalls4 reports
- 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.
How reports and recalls are matched · Editorial policy · Report an error on this page