REUNIONRecalls & reported problems across all models
Stryker GmbH · 113 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 473
- Deaths reported
- 0
- Injuries reported
- 357
- Recalls
- 0
We found 113 models of REUNION by Stryker GmbH in the FDA's device registry (GUDID). Together they are named in 473 adverse event reports in the FDA's MAUDE database, received between Sep 20, 2017 and Sep 18, 2026 — classified as 357 injuries, 116 malfunctions.
The most frequently reported specific device problem is “Fracture” (74 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. 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
Reports received per month, all models
Most reported REUNION problems
Device problems
- Adverse Event Without Identified Device or Use Problem198
- Fracture74
- Break69
- Device Dislodged or Dislocated60
- Detachment of Device or Device Component16
- Loose or Intermittent Connection13
- Migration12
- Naturally Worn12
Patient problems
- No Known Impact Or Consequence To Patient69
- Implant Pain56
- Discomfort43
- No Clinical Signs, Symptoms or Conditions39
- Bone Fracture(s)38
- Loss of Range of Motion38
- Injury36
- Failure of Implant35
REUNION models
113 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- REUNION 5901-1168PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED48 reports
- REUNION 5572-4516PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED39 reports
- REUNION 5572-2800PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED33 reports
- REUNION 5572-4524PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED20 reports
- REUNION 5570-3604PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED16 reports
- REUNION 5572-4528PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED16 reports
- REUNION 5572-4532PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED16 reports
- REUNION 5573-6528PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED11 reports
- REUNION 5573-C-3202PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED11 reports
- REUNION 5571-S-3604PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED10 reports
- REUNION 5572-4520PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED10 reports
- REUNION 5572-4540PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED10 reports
- REUNION 5573-C-3606PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED10 reports
- REUNION 5570-3204PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED9 reports
- REUNION 5572-4536PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED9 reports
- REUNION 5573-6524PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED8 reports
- REUNION 5573-C-3602PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED8 reports
- REUNION 5569-P-2013PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED7 reports
- REUNION 5570-3610PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED7 reports
- REUNION 5573-6536PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED7 reports
- REUNION 5573-2E-3606PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED7 reports
- REUNION 5567-P-3013PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED7 reports
- REUNION 5901-C-3202PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED6 reports
- REUNION 5571-S-3606PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED5 reports
- REUNION 5573-6532PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED5 reports
- REUNION 5573-2E-3602PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED5 reports
- REUNION 5573-C-3206PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED5 reports
- REUNION 5901-1122PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED5 reports
- REUNION 5571-S-3206PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED4 reports
- REUNION 5572-4544PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED4 reports
- REUNION 5901-IS-3204PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED4 reports
- REUNION 5552-E-4416PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED3 reports
- REUNION 5570-4004PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED3 reports
- REUNION 5571-S-3204PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED3 reports
- REUNION 5901-E-5220ORTHOPEDIC MANUAL SURGICAL INSTRUMENT3 reports
- REUNION 5567-P-3014PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED3 reports
- REUNION 5542-P-0048PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED2 reports
- REUNION 5542-K-0040PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED2 reports
- REUNION 5552-S-4419PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED2 reports
- REUNION 5552-S-5217PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED2 reports
- REUNION 5552-E-5217PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED2 reports
- REUNION 5569-P-2014PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED2 reports
- REUNION 5570-3210PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED2 reports
- REUNION 5571-S-3208PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED2 reports
- REUNION 5571-C-3206PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED2 reports
- REUNION 5573-6544PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED2 reports
- REUNION 5901-1103ORTHOPEDIC MANUAL SURGICAL INSTRUMENT2 reports
- REUNION 5901-1120ORTHOPEDIC MANUAL SURGICAL INSTRUMENT2 reports
- REUNION 5901-E-5223ORTHOPEDIC MANUAL SURGICAL INSTRUMENT2 reports
- REUNION 5901-S-5217ORTHOPEDIC MANUAL SURGICAL INSTRUMENT2 reports
- REUNION 5567-P-3017PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED2 reports
- REUNION 5567-P-3009PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED2 reports
- REUNION 5567-P-3010PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED2 reports
- REUNION 5567-P-3012PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED2 reports
- REUNION 5572-2802PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED2 reports
- REUNION 5542-P-0040PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- REUNION 5542-P-0056PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- REUNION 5552-S-4416PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- REUNION 5552-S-5622PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- REUNION 5552-S-5628PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- REUNION 5552-E-4821PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- REUNION 5569-P-2008PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- REUNION 5569-P-2011PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- REUNION 5569-P-2012PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- REUNION 5569-P-2015PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- REUNION 5571-S-3608PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- REUNION 5571-S-3610PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- REUNION 5571-S-4004PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- REUNION 5571-C-3204PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- REUNION 5571-C-3606PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- REUNION 5571-C-3608PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- REUNION 5571-C-3610PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- REUNION 5571-C-3612PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- REUNION 5571-C-4008PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- REUNION 5573-C-4002PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- REUNION 5573-4E-4006PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- REUNION 5901-1252ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- REUNION 5901-0028ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- REUNION 5901-0025ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- REUNION 5901-1038ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- REUNION 5901-1111ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- REUNION 5901-E-4422ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- REUNION 5901-E-4419ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- REUNION 5901-E-4821ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- REUNION 5901-E-5217PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- REUNION 5901-E-5226ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- REUNION 5901-E-5619ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- REUNION 5901-S-4419ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- REUNION 5901-S-4815ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- REUNION 5901-S-5220ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- REUNION 5901-S-5226ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- REUNION 5901-S-5625ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- REUNION 5901-S-5628ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- REUNION 5901-1119PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- REUNION 5901-1195PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- REUNION 5901-1101PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- REUNION 5901-1116PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- REUNION 5901-1184PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- REUNION 5901-4E-4002PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- REUNION 5901-C-3602PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
Recent REUNION adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjurySep 18, 2026Device Dislodged or Dislocated
A revision surgery was performed as the device was dislocated and causing pain.
Patient problems: Joint Dislocation; Pain
MAUDE report 50818653 ↗InjurySep 14, 2026Device Dislodged or Dislocated
Patient problems: Joint Dislocation; Pain
MAUDE report 50763649 ↗InjurySep 14, 2026Device Dislodged or Dislocated
Patient problems: Joint Dislocation; Pain
MAUDE report 50763395 ↗InjurySep 14, 2026Device Dislodged or Dislocated
Patient problems: Joint Dislocation; Pain
MAUDE report 50763391 ↗InjurySep 10, 2026Insufficient Device Problem Information
A Stryker Reunion Reverse shoulder implant was revised using new Stryker Reunion implants.
Patient problems: Insufficient Information
MAUDE report 50716217 ↗InjurySep 10, 2026Insufficient Device Problem Information
A Stryker Reunion Reverse shoulder implant was revised using new Stryker Reunion implants.
Patient problems: Insufficient Information
MAUDE report 50714930 ↗InjurySep 8, 2026Fracture
It was reported that during a revision of a left ReUnion reverse shoulder arthroplasty, the tip of the center screw and one peripheral screw from the primary procedure were found to be broken. The existing components were revised and replaced with a new Stryker ReUnion baseplate, screws, cup, liner, and glenosphere.
Patient problems: Insufficient Information
MAUDE report 50673886 ↗InjurySep 8, 2026Adverse Event Without Identified Device or Use Problem
It was reported that during a revision of a left ReUnion reverse shoulder arthroplasty, the tip of the center screw and one peripheral screw from the primary procedure were found to be broken. The existing components were revised and replaced with a new Stryker ReUnion baseplate, screws, cup, liner, and glenosphere.
Patient problems: Insufficient Information
MAUDE report 50672937 ↗InjurySep 8, 2026Adverse Event Without Identified Device or Use Problem
It was reported that during a revision of a left ReUnion reverse shoulder arthroplasty, the tip of the center screw and one peripheral screw from the primary procedure were found to be broken. The existing components were revised and replaced with a new Stryker ReUnion baseplate, screws, cup, liner, and glenosphere.
Patient problems: Insufficient Information
MAUDE report 50672936 ↗InjurySep 8, 2026Fracture
It was reported that during a revision of a left ReUnion reverse shoulder arthroplasty, the tip of the center screw and one peripheral screw from the primary procedure were found to be broken. The existing components were revised and replaced with a new Stryker ReUnion baseplate, screws, cup, liner, and glenosphere.
Patient problems: Insufficient Information
MAUDE report 50672935 ↗InjurySep 8, 2026Adverse Event Without Identified Device or Use Problem
It was reported that during a revision of a left ReUnion reverse shoulder arthroplasty, the tip of the center screw and one peripheral screw from the primary procedure were found to be broken. The existing components were revised and replaced with a new Stryker ReUnion baseplate, screws, cup, liner, and glenosphere.
Patient problems: Insufficient Information
MAUDE report 50672933 ↗InjuryAug 24, 2026Improper or Incorrect Procedure or Method
A reunion stem was implanted by mistake and was revised in the same day.
Patient problems: Insufficient Information
MAUDE report 50412880 ↗InjuryMar 4, 2026Device Dislodged or Dislocated
A REVISION SURGERY WAS PERFORMED DUE TO DISASSOCIATION OF THE GLENOSPHERE.
Patient problems: Joint Dislocation
MAUDE report 24507240 ↗InjuryJan 28, 2026Adverse Event Without Identified Device or Use Problem
THE PATIENT UNDERWENT REVISION SURGERY INVOLVING REMOVAL OF THE REUNION GLENOID COMPONENTS AND IMPLANTATION OF A HUMERAL HEMIARTHROPLASTY HEAD.
Patient problems: Bone Fracture(s); Fall; No Clinical Signs, Symptoms or Conditions
MAUDE report 24198337 ↗InjuryJan 27, 2026Adverse Event Without Identified Device or Use Problem
THE PATIENT UNDERWENT REVISION SURGERY INVOLVING REMOVAL OF THE REUNION GLENOID COMPONENTS AND IMPLANTATION OF A HUMERAL HEMIARTHROPLASTY HEAD.
Patient problems: Bone Fracture(s); Fall; No Clinical Signs, Symptoms or Conditions
MAUDE report 24191128 ↗
Other Stryker GmbH products
All Stryker GmbH devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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