Clavicle Plates CPSMIDR-8Recalls & reported problems
Trimed, INC. · Superior Midshaft Plate, Rt, 8-Hole · Class 2 · Implant
Data updated Oct 16, 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 00842188100369), received between Nov 20, 2020 and Nov 20, 2020 — classified as 1 injury.
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 16, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Implant Pain1
- Nonunion/Delayed-union Bone Fracture1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 20, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
A TRIMED SALES REP LOCATED IN (B)(6) REPORTED ON 22 OCT 2020 THAT A PLATE (CPSMIDR-8) HAD TO BE REMOVED FROM A PATIENT BECAUSE OF A NONUNION. THE PLATE WAS ORIGINALLY IMPLANTED ON (B)(6) 2020, AND THE PATIENT STARTED BEGIN FEELING DISCOMFORT ON (B)(6) 2020. IT WAS DETERMINED ON (B)(6) 2020 THAT THE PLATE WOULD NEED TO BE REMOVED DUE TO THE NONUNION. IT WAS STATED THAT THE PATIENT WAS A HEAVY SMOKER AND NOT FOLLOWING PROPER AFTER CARE INSTRUCTIONS.
Patient problems: Implant Pain; Nonunion/Delayed-union Bone Fracture
MAUDE report 10880311 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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