Minima S Instrument Set Trial Modular NeckRecalls & reported problems
Limacorporate SPA · Trial Modular Neck #5 · Class 2
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 08033390085014), received between May 6, 2025 and May 6, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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.
Reports received per month
Most reported problems
Device problems
- Device Dislodged or Dislocated1
- Mechanical Problem1
Patient problems
- Joint Dislocation1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 6, 2025Mechanical Problem; Device Dislodged or Dislocated; Mechanical Problem; Device Dislodged or Dislocated
SHOULDER REVISION SURGERY WAS PERFORMED ON (B)(6) 2025, DUE TO IMPLANT DISLOCATION. THE PATIENT HAD PREVIOUS REVERSE SHOULDER SURGERY ON (B)(6) 2025. IT WAS REPORTED THAT THE PATIENT DISLOCATED SOMETIME AFTER, AND THE DOCTOR DECIDED TO REVISE THE MODULAR PARTS TO HELP PREVENT POSSIBLE FUTURE DISLOCATION. THE FOLLOWING COMPONENTS WERE REMOVED: - SMR REVERSE LINER STD D.40MM (PART CODE 1365.50.810, LOT NUMBER 23AT07N, STERILIZATION (B)(4)). - SMR CONNECTOR SMALL STD (PART CODE 1374.15.310, LOT NUMBER 2418873, STERILIZATION (B)(4)). - SMR ECCENT. GLENOSPHERE DIA. 40MM (PART CODE 1376.09.041, LOT NUMBER 2433287, STERILIZATION (B)(4)). THE ABOVE-MENTIONED COMPONENTS WERE REPLACED BY THE FOLLOWING NEW ONES: - SMR CONNECTOR SMALL STD +4MM (PART CODE 1374.15.324, LOT NUMBER 2202384, STERILIZATION (B)(4)). - SMR REVERSE LINER RET. +3 MM (PART CODE 1365.50.816, LOT NUMBER 23AT1TE, STERILIZATION (B)(4)). - SMR ECCENT. GLENOSPHERE DIA. 40MM (PART CODE 1376.09.041, LOT NUMBER 2314910, STERILIZATION (B)(4)). THE PATIENT IS A MALE, DATE OF BIRTH (B)(6) 1963. THE EVENT HAPPENED IN THE UNITED STATES.
Patient problems: Joint Dislocation; No Clinical Signs, Symptoms or Conditions
MAUDE report 21967669 ↗
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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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