MSP Metatarsal Shortening Plate Kit MS-SSRRecalls & reported problems
Medartis Inc. · 36.5mm MSP Right Plate Kit · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00817701020103), received between Jul 22, 2019 and Nov 20, 2019 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Break” (4 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 18, 2026.
Most reported problems
Device problems
- Break4
Patient problems
- No Known Impact Or Consequence To Patient4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 20, 2019Break; Break
IT WAS REPORTED THAT DURING SURGERY USING THE MSP METATARSAL SHORTENING SYSTEM, THE TIP OF THE DRIVER BROKE OFF INTO THE HEAD OF THE SCREW. THE CUSTOMER USED A BACKUP DRIVER TO INSERT THE SCREW AND THE DRIVER TIP BROKE AGAIN IN THE SAME WAY. NO PATIENT COMPLICATIONS WERE REPORTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9346844 ↗MalfunctionNov 15, 2019Break; Break
IT WAS REPORTED THAT DURING A SURGERY USING THE MSP METATARSAL SHORTENING SYSTEM, THE SCREWDRIVER TIP BROKE OFF INTO THE HEAD OF THE SCREW. THE TIP OF THE DRIVER WAS NOT REMOVED FROM THE SCREW. THE SCREW REMAINS IMPLANTED. NO PATIENT COMPLICATIONS WERE REPORTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9329846 ↗MalfunctionOct 11, 2019Break; Break
IT WAS REPORTED THAT DURING SURGERY USING THE MSP METATARSAL SHORTENING SYSTEM, THE SCREW DRIVER TIP BROKE OFF INTO THE HEAD OF THE SCREW DURING FINAL TIGHTENING OF THE SCREW. THE TIP OF THE DRIVER WAS NOT REMOVED. THE SURGERY WAS COMPLETED . NO PATIENT COMPLICATIONS WERE REPORTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9180845 ↗MalfunctionJul 22, 2019Break; Break
IT WAS REPORTED THAT DURING SURGERY THE TIP OF THE DRIVER BROKE OFF INSIDE THE HEAD OF THE SCREW AND WAS NOT REMOVED. THE SURGERY WAS ABLE TO BE COMPLETED SUCCESSFULLY. NO PATIENT COMPLICATIONS WERE REPORTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8812319 ↗
Other Plate, Fixation, Bone devices
- Lapiplasty System 2 SK14Treace Medical Concepts, Inc. · Plate, Fixation, Bone260 reports
- PRECICE® Plating System LP4.5-PRF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls6 reports
- PRECICE® Plating System LP4.5-MLT4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls5 reports
- PRECICE® Plating System LP4.5-MRT4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- PRECICE® Plating System LP4.5-PLF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- PRECICE® Plating System LP4.5-DRF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls1 report
- PRECICE® Plating System LP4.5-MLT42Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 reports
- PRECICE® Plating System LP4.5-MRT42Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 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 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 18, 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