NA 02.205.075Recalls & reported problems
Synthes GmbH · 5.0MM CANNULATED LOCKING SCREW 75MM · Class 2 · Implant
Data updated Oct 18, 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 10886982049773), received between Jan 23, 2019 and Jan 23, 2019 — classified as 1 injury.
The most frequently reported specific device problem is “Material Twisted/Bent” (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 18, 2026.
Most reported problems
Device problems
- Material Twisted/Bent1
- Migration1
Patient problems
- No Code Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJan 23, 2019Material Twisted/Bent; Migration; Material Twisted/Bent; Migration
IT WAS REPORTED THAT A PATIENT UNDERWENT A REMOVAL SURGERY ON (B)(6) 2018. ONE (1) 70MM CANNULATED VARIABLE ANGLE (VA) LOCKING SCREW, ONE (1) 75MM CANNULATED VA LOCKING SCREWS, TWO (2) 80MM CANNULATED VA LOCKING SCREWS AND ONE (1) 85MM CANNULATED VA LOCKING SCREW HAD BACKED OUT OF THE CONDYLAR PLATE AND WERE REMOVED. THE PLATE WAS RETAINED, AND NEW SCREWS WERE ADDED. THE VARIABLE ANGLE LOCKING COMPRESSION PLATE (LCP) CONDYLAR PLATE WAS ORIGINALLY IMPLANTED ON (B)(6) 2018. PROCEDURE OUTCOME AND PATIENT STATUS IS UNKNOWN. CONCOMITANT DEVICES: CONDYLAR PLATE (PART: UNKNOWN, LOT: UNKNOWN, QUANTITY 1), LOCKING SPINE SCREW (PART: UNKNOWN, LOT: UNKNOWN, QUANTITY 1). THIS REPORT IS FOR A 5.0MM CANNULATED LOCKING SCREW 75MM. THIS IS REPORT 3 OF 5 FOR (B)(4).
Patient problems: No Code Available
MAUDE report 8271931 ↗
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- HEALIX PEEK ORTHOCORD 222205Medos International Sàrl · Screw, fixation, bone186 reports
- PRECICE® Bone Transport System STP3.5-400Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-225Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-350Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-300Nuvasive Specialized Orthopedics, Inc. · Screw, 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.
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