GLOBAL ICON 1140-20-046Recalls & reported problems

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10603295381242), received between Jan 16, 2019 and Aug 5, 2021 — classified as 6 injuries.

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.

Most reported problems

Recent adverse event reports

The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

• InjuryAug 5, 2021Adverse Event Without Identified Device or Use Problem; Appropriate Device Problem Term/Code Not Available; Adverse Event Without Identified Device or Use Problem; Appropriate Device Problem Term/Code Not Available

  CLINICAL ADVERSE EVENT RECEIVED FOR BICEPS TENDONITIS AFTER TENODESIS. EVENT IS NOT SERIOUS AND IS CONSIDERED MILD. EVENT IS POSSIBLY RELATED TO DEVICE AND PROCEDURE. DATE OF IMPLANTATION: (B)(6) 2019, DATE OF EVENT (ONSET): (B)(6) 2020, (RIGHT SHOULDER). TREATMENT: MEDICAL INTERVENTION/MODIFICATION (DETAILS UNSPECIFIED).

  Patient problems: Inflammation; Muscle/Tendon Damage

  MAUDE report 12283042 ↗
• InjuryMar 4, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  CLINICAL ADVERSE EVENT RECEIVED FOR PAIN AND STIFFNESS LEFT SHOULDER. EVENT IS NOT SERIOUS AND IS CONSIDERED MILD. EVENT IS POSSIBLY RELATED TO BOTH DEVICE AND IS DEFINITELY RELATED TO PROCEDURE.. DATE OF IMPLANTATION: (B)(6) 2019. DATE OF EVENT (ONSET): (B)(6) 2020. (LEFT SHOULDER). TREATMENT: MEDICAL INTERVENTION/MODIFICATION (UNSPECIFIED): YES. DIAGNOSTIC INTERVENTION (UNSPECIFIED): YES. PHYSICAL THERAPY: YES.

  Patient problems: No Code Available; Pain

  MAUDE report 9788496 ↗
• InjuryJan 23, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  CLINICAL ADVERSE EVENT RECEIVED FOR DORSAL SUBLUXATION; EVENT IS SERIOUS AND IS CONSIDERED SEVERE. EVENT IS DEFINITELY RELATED TO BOTH DEVICE AND PROCEDURE. DATE OF IMPLANTATION: (B)(6) 2019; DATE OF EVENT (ONSET): (B)(6) 2020; (RIGHT SHOULDER). TREATMENT: DIAGNOSTIC INTERVENTION (UNSPECIFIED) ONLY

  Patient problems: No Code Available; Pain

  MAUDE report 9623649 ↗
• InjuryDec 26, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  CLINICAL ADVERSE EVENT RECEIVED FOR PERSISTENT PAIN. EVENT IS NOT SERIOUS AND IS CONSIDERED MODERATE. EVENT IS DEFINITELY NOT RELATED TO DEVICE AND IS POSSIBLY RELATED TO PROCEDURE. DATE OF IMPLANTATION: (B)(6) 2019; DATE OF EVENT (ONSET): (B)(6) 2019; (LEFT SHOULDER).

  Patient problems: No Code Available; Pain

  MAUDE report 9520902 ↗
• InjuryNov 6, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  CLINICAL ADVERSE EVENT RECEIVED FOR BURSITIS. EVENT IS SERIOUS AND IS CONSIDERED MODERATE. EVENT IS DEFINITELY NOT RELATED TO DEVICE AND IS PROBABLY RELATED TO PROCEDURE. DATE OF IMPLANTATION: (B)(6) 2019; DATE OF EVENT (ONET): (B)(6) 2019; (RIGHT SHOULDER).

  Patient problems: No Code Available

  MAUDE report 9287759 ↗
• InjuryJan 16, 2019Device Dislodged or Dislocated; Device Dislodged or Dislocated

  POSTERIOR SUBLUXATIONS OF THE SHOULDER PERSISTED, SO THAT REVISION ARTHROPLASTY TO A REVERSE SHOULDER IMPLANT WITH A GLENOID BONE GRAFT WAS PERFORMED.

  Patient problems: Joint Dislocation; No Code Available

  MAUDE report 8252411 ↗