CannCompScrew 5.5mm (SelfDrill) L5556Recalls & reported problems
Trimed, INC. · Self-Drill CCScrew LThd 5.5, 56mm · Class 2 · Implant
Data updated Oct 18, 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 00842188103681), received between Oct 19, 2018 and Oct 19, 2018 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fracture” (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
- Fracture1
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.
MalfunctionOct 19, 2018Fracture; Fracture
TRIMED RECEIVED THE FOLLOWING REPORT ON (B)(6) 2018 FROM TRIMED SALES MEMBER LOCATED IN AUSTRALIA, REGARDING THE SELF-DRILL CANNULATED COMPRESSION SCREW L THD 5.5, 56MM: DURING A INTRA-OPERATIVE PROCEDURE, IT WAS DISCOVERED THAT THE SELF-DRILL CANNULATED COMPRESSION SCREW L THD 5.5, 56MM (L5556) HAD THE SCREW END SNAP OFF HALFWAY THROUGH INSERTING INTO THE BONE. ALL PARTS OF THE SCREW WERE RECOVERED FROM THE PATIENT. IT WAS DETERMINED THAT THE BONE WAS QUITE SCLEROTIC COMPARED TO USUAL. THIS INCIDENT DID NOT CAUSE ANY FURTHER HARM TO THE PATIENT. THIS IS THE FIRST TIME THIS TYPE OF MALFUNCTION HAS BEEN REPORTED TO TRIMED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7987523 ↗
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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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