ACHIEVECAS 74473200Recalls & reported problems
Smith & Nephew, Inc. · COVE POINT PIN 120MMX28MMX3MM STERILE · Class 2
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 00885556074527), received between May 29, 2019 and May 29, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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
- Break1
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.
MalfunctionMay 29, 2019Break; Break
IT WAS REPORTED THAT DURING THR THE PIN SHEERED OFF DURING PLACEMENT AT JUNCTION OF THREADS AND SHAFT OF PIN. THE THREADED PORTION OF THE PIN REMAINS IN PATIENT AT THE ANTERIOR SUPERIOR ILIAC SPINE. DELAY OF LESS THAN 30 MIN REPORTED. A BACK UP DEVICE WAS AVAILABLE. NO PROCEDURE OR MEDICAL INTERVENTION REPORTED TO RETRIEVE THE FRAGMENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8651097 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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