Tornier Perform Reversed GlenoidRecalls & reported problems across all models

We found 41 models of Tornier Perform Reversed Glenoid by Tornier, Inc. in the FDA's device registry (GUDID). Together they are named in 515 adverse event reports in the FDA's MAUDE database, received between Jan 10, 2022 and Sep 29, 2026 — classified as 497 injuries, 18 malfunctions.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (76 reports).

1 FDA recall record name at least one of these models by its device identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

Tornier Perform Reversed Glenoid recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

1. Jan 3, 2024Open, Classified

   The incorrect device is contained in the labeled package.

   Z-0773-2024 · Root cause: Packaging process control · Recall details · FDA record ↗

Most reported Tornier Perform Reversed Glenoid problems

Tornier Perform Reversed Glenoid models

41 models, most reported first. Each model has its own page with its reports, recalls and device details.

• Tornier Perform® Reversed Glenoid DWJ012

  PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
  98 reports
• Tornier Perform® Reversed Glenoid DWJ401

  PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
  64 reports
• Tornier Perform® Reversed Glenoid DWJ001

  PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
  1 recall12 reports
• Tornier Perform® Reversed Glenoid DWJ013

  PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
  60 reports
• Tornier Perform® Reversed Glenoid DWJ014

  shoulder prosthesis, reverse configuration
  33 reports
• Tornier Perform® Reversed Glenoid DWJ330

  PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
  17 reports
• Tornier Perform® Reversed Glenoid DWJ023

  shoulder prosthesis, reverse configuration
  16 reports
• Tornier Perform® Reversed Glenoid DWJ738

  shoulder prosthesis, reverse configuration
  13 reports
• Tornier Perform® Reversed Glenoid DWJ718

  shoulder prosthesis, reverse configuration
  12 reports
• Tornier Perform® Reversed Glenoid DWJ730

  PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
  12 reports
• Tornier Perform® Reversed Glenoid DWJ722

  shoulder prosthesis, reverse configuration
  11 reports
• Tornier Perform® Reversed Glenoid DWJ734

  shoulder prosthesis, reverse configuration
  11 reports
• Tornier Perform® Reversed Glenoid DWJ411

  shoulder prosthesis, reverse configuration
  11 reports
• Tornier Perform® Reversed Glenoid DWJ326

  shoulder prosthesis, reverse configuration
  10 reports
• Tornier Perform® Reversed Glenoid DWJ033

  PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
  10 reports
• Tornier Perform® Reversed Glenoid DWJ022

  PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
  9 reports
• Tornier Perform® Reversed Glenoid DWJ024

  PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
  9 reports
• Tornier Perform® Reversed Glenoid DWJ002

  shoulder prosthesis, reverse configuration
  8 reports
• Tornier Perform® Reversed Glenoid DWJ135

  PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
  7 reports
• Tornier Perform® Reversed Glenoid DWJ338

  PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
  7 reports
• Tornier Perform® Reversed Glenoid DWJ334

  shoulder prosthesis, reverse configuration
  7 reports
• Tornier Perform® Reversed Glenoid DWJ322

  PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
  7 reports
• Tornier Perform® Reversed Glenoid DWJ034

  shoulder prosthesis, reverse configuration
  7 reports
• Tornier Perform® Reversed Glenoid DWJ726

  shoulder prosthesis, reverse configuration
  7 reports
• Tornier Perform® Reversed Glenoid DWJ318

  shoulder prosthesis, reverse configuration
  6 reports
• Tornier Perform® Reversed Glenoid DWJ530

  shoulder prosthesis, reverse configuration
  6 reports
• Tornier Perform® Reversed Glenoid DWJ742

  PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
  6 reports
• Tornier Perform® Reversed Glenoid DWJ540

  shoulder prosthesis, reverse configuration
  5 reports
• Tornier Perform® Reversed Glenoid DWJ032

  shoulder prosthesis, reverse configuration
  4 reports
• Tornier Perform® Reversed Glenoid DWJ535

  PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
  4 reports
• Tornier Perform® Reversed Glenoid DWJ714

  PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
  4 reports
• Tornier Perform® Reversed Glenoid DWJ342

  PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
  3 reports
• Tornier Perform® Reversed Glenoid DWJ130

  PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
  3 reports
• Tornier Perform® Reversed Glenoid DWJ346

  shoulder prosthesis, reverse configuration
  3 reports
• Tornier Perform® Reversed Glenoid DWJ140

  PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
  3 reports
• Tornier Perform® Reversed Glenoid DWJ125

  shoulder prosthesis, reverse configuration
  3 reports
• Tornier Perform® Reversed Glenoid DWJ314

  PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
  2 reports
• Tornier Perform® Reversed Glenoid DWJ021

  PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
  2 reports
• Tornier Perform® Reversed Glenoid DWJ230

  shoulder prosthesis, reverse configuration
  1 report
• Tornier Perform® Reversed Glenoid DWJ545

  shoulder prosthesis, reverse configuration
  1 report
• Tornier Perform® Reversed Glenoid DWJ750

  PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
  1 report

Recent Tornier Perform Reversed Glenoid adverse event reports

The 15 most recent reports across all models, in the reporter's own words as published by the FDA.

• InjurySep 29, 2026Unstable

  As reported: "Patients shoulder became unstable six months after initial RSA surgery so surgeon performed a revision surgery to exchange the 39mm Glenosphere and 45% reverse poly insert."

  Patient problems: Joint Laxity

  MAUDE report 50934359 ↗
• InjurySep 18, 2026Device Dislodged or Dislocated

  The manufacturer received a report from the National Joint Registry that contains unpublished collected data on the usage and the outcomes of the shoulder joint replacement. The report details analysis provided for revision procedures performed until Aug 2026.During the review of the report, it was identified that on (b)(6) 2025 a patient required revision surgery due to INFECTION, DISLOCATION/SUBLUXATION, which was not previously reported to the manufacturer.

  Patient problems: Subluxation; Unspecified Infection

  MAUDE report 50820937 ↗
• InjurySep 18, 2026Device Dislodged or Dislocated

  The manufacturer received a report from the National Joint Registry that contains unpublished collected data on the usage and the outcomes of the shoulder joint replacement. The report details analysis provided for revision procedures performed until Aug 2026.During the review of the report, it was identified that on (b)(6) 2025 a patient required revision surgery due to INFECTION, DISLOCATION/SUBLUXATION, which was not previously reported to the manufacturer.

  Patient problems: Subluxation; Unspecified Infection

  MAUDE report 50820936 ↗
• InjurySep 18, 2026Device Dislodged or Dislocated

  Patient problems: Osteolysis; Subluxation

  MAUDE report 50819508 ↗
• InjurySep 17, 2026Unstable

  The manufacturer received a report from the National Joint Registry that contains unpublished collected data on the usage and the outcomes of the shoulder joint replacement. The report details analysis provided for revision procedures performed until (b)(6) 2026.During the review of the report, it was identified that on (b)(6) 2026 a patient required revision surgery due to instability, which was not previously reported to the manufacturer.

  Patient problems: Joint Laxity

  MAUDE report 50803927 ↗
• InjurySep 17, 2026Adverse Event Without Identified Device or Use Problem

  The manufacturer received a report from the National Joint Registry that contains unpublished collected data on the usage and the outcomes of the shoulder joint replacement. The report details analysis provided for revision procedures performed until (b)(6) 2026.During the review of the report, it was identified that on (b)(6) 2026 a patient required revision surgery due to infection & lysis- glenoid, which was not previously reported to the manufacturer.

  Patient problems: Osteolysis; Unspecified Infection

  MAUDE report 50803906 ↗
• InjurySep 16, 2026Adverse Event Without Identified Device or Use Problem

  As reported: "Patient has re-presented to surgeon, following revision shoulder arthroplasty in (b)(6)2026. Significant swelling and redness over wound, pain on movement. Wound re-opened, and surgeon concluded that the prosthetic joint was now infected. Decided to remove all prosthesis, as stage 1 of a 2-stage revision. Glenoid component was found to be very loose, easily removed as 1 x construct (revised at previous revision). Humeral component (not revised at previous revision) was found to be extremely well fixed. Humeral poly insert removed - significant wear noted (only been insitu since (b)(6) 2026 revision). Proximal humeral vertical osteotomy was required to loosen and to break the bone / implant ongrowth. Stem eventually removed; osteotomy cabled back together with Nice Loops. Multiple tissue specimens collected; debridement; copious lavage attended; no antibiotic spacer implanted - gleno-humeral joint left dis-articulated.Plan - antibiotic regime until clinical markers indicate no infection, then the 2nd stage revision will be undertaken, using a "Custom Glenoid", to be manufactured by a competitor company."

  Patient problems: Pain; Swelling/ Edema; Unspecified Infection

  MAUDE report 50791182 ↗
• InjurySep 16, 2026Adverse Event Without Identified Device or Use Problem

  As reported: "Patient has re-presented to surgeon, following revision shoulder arthroplasty in (b)(6) 2026. Significant swelling and redness over wound, pain on movement. Wound re-opened, and surgeon concluded that the prosthetic joint was now infected. Decided to remove all prosthesis, as stage 1 of a 2-stage revision. Glenoid component was found to be very loose, easily removed as 1 x construct (revised at previous revision). Humeral component (not revised at previous revision) was found to be extremely well fixed. Humeral poly insert removed - significant wear noted (only been insitu since (b)(6) '26 revision). Proximal humeral vertical osteotomy was required to loosen and to break the bone / implant on growth. Stem eventually removed; osteotomy cabled back together with Nice Loops. Multiple tissue specimens collected; debridement; copious lavage attended; no antibiotic spacer implanted - gleno-humeral joint left dis-articulated.Plan - antibiotic regime until clinical markers indicate no infection, then the 2nd stage revision will be undertaken, using a "Custom Glenoid", to be manufactured by a competitor company."

  Patient problems: Pain; Swelling/ Edema; Unspecified Infection

  MAUDE report 50791181 ↗
• InjurySep 16, 2026Adverse Event Without Identified Device or Use Problem

  As reported: "Patient has re-presented to surgeon, following revision shoulder arthroplasty in (b)(6), 2026. Significant swelling and redness over wound, pain on movement. Wound re-opened, and surgeon concluded that the prosthetic joint was now infected. Decided to remove all prosthesis, as stage 1 of a 2-stage revision. Glenoid component was found to be very loose, easily removed as 1 x construct (revised at previous revision). Humeral component (not revised at previous revision) was found to be extremely well fixed. Humeral poly insert removed - significant wear noted (only been insitu since (b)(6)2026 revision). Proximal humeral vertical osteotomy was required to loosen and to break the bone / implant ongrowth. Stem eventually removed; osteotomy cabled back together with Nice Loops. Multiple tissue specimens collected; debridement; copious lavage attended; no antibiotic spacer implanted - gleno-humeral joint left dis-articulated.Plan - antibiotic regime until clinical markers indicate no infection, then the 2nd stage revision will be undertaken, using a "Custom Glenoid", to be manufactured by a competitor company."

  Patient problems: Pain; Swelling/ Edema; Unspecified Infection

  MAUDE report 50791173 ↗
• InjurySep 16, 2026Adverse Event Without Identified Device or Use Problem

  As reported: "Patient has re-presented to surgeon, following revision shoulder arthroplasty in (b)(6)2026. Significant swelling and redness over wound, pain on movement. Wound re-opened, and surgeon concluded that the prosthetic joint was now infected. Decided to remove all prosthesis, as stage 1 of a 2-stage revision. Glenoid component was found to be very loose, easily removed as 1 x construct (revised at previous revision). Humeral component (not revised at previous revision) was found to be extremely well fixed. Humeral poly insert removed - significant wear noted (only been insitu since (b)(6)2026 revision). Proximal humeral vertical osteotomy was required to loosen and to break the bone / implant ongrowth. Stem eventually removed; osteotomy cabled back together with Nice Loops. Multiple tissue specimens collected; debridement; copious lavage attended; no antibiotic spacer implanted - gleno-humeral joint left dis-articulated.Plan - antibiotic regime until clinical markers indicate no infection, then the 2nd stage revision will be undertaken, using a "Custom Glenoid", to be manufactured by a competitor company."

  Patient problems: Pain; Swelling/ Edema; Unspecified Infection

  MAUDE report 50791168 ↗
• InjurySep 16, 2026Adverse Event Without Identified Device or Use Problem

  As reported: "Patient has re-presented to surgeon, following revision shoulder arthroplasty in (b)(6) 2026. Significant swelling and redness over wound, pain on movement. Wound re-opened, and surgeon concluded that the prosthetic joint was now infected. Decided to remove all prosthesis, as stage 1 of a 2-stage revision. Glenoid component was found to be very loose, easily removed as 1 x construct (revised at previous revision). Humeral component (not revised at previous revision) was found to be extremely well fixed. Humeral poly insert removed - significant wear noted (only been insitu since (b)(6)'26 revision). Proximal humeral vertical osteotomy was required to loosen and to break the bone / implant ongrowth. Stem eventually removed; osteotomy cabled back together with Nice Loops. Multiple tissue specimens collected; debridement; copious lavage attended; no antibiotic spacer implanted - gleno-humeral joint left dis-articulated.Plan - antibiotic regime until clinical markers indicate no infection, then the 2nd stage revision will be undertaken, using a "Custom Glenoid", to be manufactured by a competitor company."

  Patient problems: Pain; Swelling/ Edema; Unspecified Infection

  MAUDE report 50790942 ↗
• InjurySep 11, 2026Loss of Osseointegration

  Patient problems: Inadequate Osseointegration

  MAUDE report 50742277 ↗
• InjurySep 11, 2026Loosening of Implant Not Related to Bone-Ingrowth

  Patient problems: Inadequate Osseointegration

  MAUDE report 50742273 ↗
• InjurySep 11, 2026Loosening of Implant Not Related to Bone-Ingrowth

  Patient problems: Inadequate Osseointegration

  MAUDE report 50742267 ↗
• InjurySep 11, 2026Unstable

  Patient problems: Insufficient Information

  MAUDE report 50735225 ↗

Other Tornier, Inc. products

• Tornier Perform40 models · 290 reports · 1 recall
• TORNIER PERFORM HUMERAL SYSTEM68 models · 190 reports · 1 recall
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• AEQUALIS FLEX REVIVE24 models · 70 reports · 2 recalls
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