Easytech Anatomical Shoulder System 314-0038Recalls & reported problems

Summary

The FDA's MAUDE database contains 14 adverse event reports that list this exact device (DI 03701037301487), received between Oct 22, 2021 and Sep 14, 2026 — classified as 14 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (5 reports).

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

Recent adverse event reports

The 14 most recent of 14 reports, in the reporter's own words as published by the FDA.

• InjurySep 14, 2026Adverse Event Without Identified Device or Use Problem

  Patient problems: Medical device site infection

  MAUDE report 50764164 ↗
• InjuryJun 24, 2026Adverse Event Without Identified Device or Use Problem

  THE PATIENT WAS REVISED DUE TO LOOSENING ON (B)(6) 2026? IT IS EVIDENTLY AN ISSUE WITH THE INITIAL POSITIONING OF THE IMPLANTS THAT LIKELY CAUSED EXCESSIVE STRESS AND, ULTIMATELY, LOOSENING OF THE PROSTHETIC GLENOID COMPONENT. THE IMPLANTATION DATE WAS ON (B)(6) 2025. AN EASYTECH ANCHOR BASE, AN EXCENTRIC HEAD, A 2 PEGS GLENOID AND A DOUBLE TAPER WERE EXPLANTED. A CUP, A GLENOSPHERE, A GLENOID BASEPLATE, SCREWS, A POST EXTENSION AND A STEM WERE IMPLANTED.

  Patient problems: Joint Laxity

  MAUDE report 25607016 ↗
• InjuryMay 20, 2026Adverse Event Without Identified Device or Use Problem

  REVISION SURGERY OCCURRED ON (B)(6) 2026. ALL REQUIRED INFORMATION WAS RECEIVED ON 13 MAY 2026. THE REVISION OCCURRED APPROXIMATELY 147 DAYS AFTER THE PRIMARY SURGERY WHICH OCCURRED ON 11-SEP-2025. NO FALL OR OTHER TRAUMA REPORTED. BASED ON COMPARING USAGE FORMS ONLY EASYTECH ANCHOR BASE TA6V Ø38 MM CEMENTLESS TI/HA, 3-4 PEGS GLENOID PE CEMENTED SIZE XS, DOUBLE TAPER TA6V +0MM 0°, AND CENTERED HEAD COCR/TIN 46X17 WAS EXPLANTED DUE TO INSTABILITY. THESE PARTS WERE REPLACED WITH HUMELOCK REVERSED TA6V CEMENTLESS GLENOID BASEPLATE W/PEG TI/HA Ø24MM, +3MM LATERALIZED, HUMELOCK REVERSED CENTERED GLENOSPHERE W/ SCREW COCR/TA6V/TIN 10° TILT Ø36MM, TWO LOCKING SCREW TA6V Ø4.5MM L.35MM, LOCKING SCREW TA6V Ø4.5MM L.30MM AND HUMERAL CUP 135/145° STABILITY PE/TA6V Ø36 +3.

  Patient problems: Joint Laxity

  MAUDE report 25234680 ↗
• InjuryJun 25, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE PATIENT WAS REVISED DUE TO A PAIN ON (B)(6) 2025. THE IMPLANTATION DATE WAS ON (B)(6) 2024. AN EASYTECH ANCHOR BASE , A DOUBLE TAPER AND AN OFFSET HEAD WERE EXPLANTED.

  Patient problems: Implant Pain

  MAUDE report 22327041 ↗
• InjuryJun 19, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE PATIENT WAS REVISED DUE TO AN INFECTION ON (B)(6) 2025. THE IMPLANTATION DATE WAS ON (B)(6) 2025.

  Patient problems: Medical device site infection

  MAUDE report 22291971 ↗
• InjuryFeb 8, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE PATIENT WAS REVISED DUE TO A LOOSENING ON (B)(6) 2024. THE IMPLANTATION DATE WAS ON (B)(6) 2019. A 2 PEGS GLENOID, A HEAD, A DOUBLE TAPER AND AN EASYTECH ANCHOR BASE WERE EXPLANTED. A CUP, A GLENOSPHERE, A METAGLENE, SCREWS, SMARTLOOPS, AN OFFSET MODULAR SYSTEM AND A STEM WERE IMPLANTED.

  Patient problems: Joint Laxity

  MAUDE report 18666042 ↗
• InjuryDec 15, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated

  THE PATIENT WILL BE REVISED DUE TO A LOOSENING ON (B)(6) 2024. THE IMPLANTATION DATE WAS ON (B)(6) 2019. AN EASYTECH ANATOMIC MAY BE EXPLANTED. AN EASYTECH REVERSED COULD BE IMPLANTED.

  Patient problems: Joint Laxity

  MAUDE report 18335420 ↗
• InjuryMay 24, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated

  THE PATIENT WAS REVISED DUE TO LOOSENING ON (B)(6) 2023. THE IMPLANTATION DATE WAS ON (B)(6) 2023. AN ANCHOR BASE WAS EXPLANTED. A HUMERAL SPACER,A CUP, A SCREW AND A STEM WERE IMPLANTED.

  Patient problems: Joint Laxity

  MAUDE report 16991363 ↗
• InjuryMar 2, 2023Unstable; Unstable

  THE PATIENT WAS REVISED DUE TO A LUXATION ON (B)(6) 2023. THE IMPLANTATION DATE WAS ON (B)(6)2022. A CUP, A GLENOSPHERE, A METAGLENE AND AN ANCHOR BASE WERE EXPLANTED. A CUP, A GLENOSPHERE, A METAGLENE AND A STEM WERE IMPLANTED.

  Patient problems: Subluxation

  MAUDE report 16468215 ↗
• InjuryMar 3, 2022Appropriate Device Problem Term/Code Not Available

  THE PATIENT WAS REVISED FOR POST-OP FRACTURE ON (B)(6) 20, 2022. APPROXIMATELY 8 MONTHS AFTER THE FIRST SURGERY. THE SURGEON EXPLANTED 1 ANCHOR BASE AND 1 HUMERAL CUP ECCENTRIC SYMMETRIC Ø36+3. THE SURGEON IMPLANTED 1 HUMELOCK REVERSED STEM Ø36/12 , 1 CAGE T40, 1 CORTICAL SCREW, 1 HUMERAL SPACER, 1 HUMERAL CUP Ø36+9 AND 1 HEX SCREW.

  Patient problems: Failure of Implant

  MAUDE report 13657965 ↗
• InjuryJan 12, 2022Device Dislodged or Dislocated; Appropriate Device Problem Term/Code Not Available

  PATIENT WAS REVISED ON (B)(6) 2021 DUE TO DISLOCATION, APPROXIMATELY 5 DAYS AFTER THE FIRST SURGERY. THE SURGEON EXPLANTED ANCHOR BASE AND SYMETRIC CUP Ø40+3. THE SURGEON IMPLANTED 135/145° Ø40+9 CUP AND HUMERIS STEM SIZE 14.

  Patient problems: Insufficient Information

  MAUDE report 13235959 ↗
• InjuryDec 24, 2021Device Dislodged or Dislocated

  PATIENT WAS REVISED ON (B)(6) 2021 DUE TO A DISLOCATION. APPROXIMATELY 5 MONTHS AFTER THE FIRST SURGERY. THE SURGEON EXPLANTED ANCHOR BASE, HUMERAL CUP 135/145 ° Ø36+6. THE SURGEON IMPLANTED STEM TA6V Ø36/14, HUMERAL CUP STABILITY 36+3.

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

  MAUDE report 13083949 ↗
• InjuryDec 16, 2021Device Dislodged or Dislocated; Appropriate Device Problem Term/Code Not Available

  PATIENT WAS REVISED ON (B)(6) 2021 FOR A DISLOCATION, APPROXIMATELY 5 DAYS AFTER THE SURGERY. THE SURGERY EXPLANTED HUMERAL CUP 36+6 AND ANCHOR BASE. THE SURGEON IMPLANTED HUMERAL CUP STABILITY 36+6 AND STEM SIZE 14.

  Patient problems: Insufficient Information

  MAUDE report 13016645 ↗
• InjuryOct 22, 2021Appropriate Device Problem Term/Code Not Available

  PATIENT WAS REVISED ON (B)(6) 2021 DUE TO INFECTION. APPROXIMATELY THREE WEEKS AFTER THE FIRST SURGERY. THE SURGEON EXPLANTED ANCHOR BASE, CENTERED HEAD, 2 PEGS GLENOID AND DOUBLE TAPER. THE SURGEON IMPLANTED THE SAME IMPLANT (ANCHOR BASE, CENTERED HEAD, 2 PEGS GLENOID AND DOUBLE TAPER).

  Patient problems: Unspecified Infection

  MAUDE report 12679492 ↗