Tornier PerformRecalls & reported problems across all models
Tornier, Inc. · 40 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names at least one Tornier Perform model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 290
- Deaths reported
- 0
- Injuries reported
- 24
- Recalls
- 1
We found 40 models of Tornier Perform by Tornier, Inc. in the FDA's device registry (GUDID). Together they are named in 290 adverse event reports in the FDA's MAUDE database, received between May 6, 2021 and Sep 29, 2026 — classified as 24 injuries, 266 malfunctions.
The most frequently reported specific device problem is “Fracture” (246 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
Reports received per month, all models
Tornier Perform 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.
- Aug 29, 2024Open, Classified
One lot of Perform Humeral Nucleus may exceed the specification for bacterial endotoxin load (max 20 EU/device).
Z-3155-2024 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Most reported Tornier Perform problems
Device problems
- Fracture246
- Break160
- Crack13
- Material Twisted/Bent13
- Adverse Event Without Identified Device or Use Problem11
- Material Fragmentation8
- Material Deformation6
- Residue After Decontamination6
Patient problems
- No Clinical Signs, Symptoms or Conditions249
- Insufficient Information20
- Foreign Body In Patient19
- Bacterial Infection3
- Implant Pain3
- Purulent Discharge3
- Unspecified Infection3
- Failure of Implant1
Tornier Perform models
40 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Tornier Perform MWJ127BIT, SURGICAL114 reports
- Tornier Perform DWM003AProsthesis, total anatomic shoulder, uncemented metaphyseal humeral stem with no diaphyseal incursion, semi-constrained1 recall1 report
- Tornier Perform MWM054IMPACTOR50 reports
- Tornier Perform MWJ123SCREWDRIVER36 reports
- Tornier Perform MWM052IMPACTOR16 reports
- Tornier Perform MWJ111INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT10 reports
- Tornier Perform MWM051IMPACTOR8 reports
- Tornier Perform MWJ128Orthopedic manual surgical instrument6 reports
- Tornier Perform MWJ130EXTRACTOR4 reports
- Tornier Perform MWJ132Orthopedic manual surgical instrument4 reports
- Tornier Perform MWM012TEMPLATE3 reports
- Tornier Perform MWM066EXTRACTOR3 reports
- Tornier Perform MWJ126BIT, SURGICAL2 reports
- Tornier Perform MWH602INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT2 reports
- Tornier Perform MWH605INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT2 reports
- Tornier Perform MWH685INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT2 reports
- Tornier Perform DWD017Guide, surgical, instrument2 reports
- Tornier Perform MWJ192INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT2 reports
- Tornier Perform MWM013TEMPLATE2 reports
- Tornier Perform MWJ109SCREWDRIVER1 report
- Tornier Perform MWJ114Guide, surgical, instrument1 report
- Tornier Perform MWJ124Guide, surgical, instrument1 report
- Tornier Perform MWJ133Orthopedic manual surgical instrument1 report
- Tornier Perform MWJ138Orthopedic manual surgical instrument1 report
- Tornier Perform MWH699SOrthopedic manual surgical instrument1 report
- Tornier Perform MWH604INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT1 report
- Tornier Perform MWH742PUNCH, SURGICAL1 report
- Tornier Perform MWH744Orthopedic manual surgical instrument1 report
- Tornier Perform MWM330IMPACTOR1 report
- Tornier Perform MWM044INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT1 report
- Tornier Perform MWM038IMPACTOR1 report
- Tornier Perform MWM011TEMPLATE1 report
- Tornier Perform MWM005Orthopedic manual surgical instrument1 report
- Tornier Perform MWM004Orthopedic manual surgical instrument1 report
- Tornier Perform MWM015Orthopedic manual surgical instrument1 report
- Tornier Perform MWP4390TEMPLATE1 report
- Tornier Perform MWP2420TEMPLATE1 report
- Tornier Perform MWP2360TEMPLATE1 report
- Tornier Perform IFX818IMPACTOR1 report
- Tornier Perform DWM001AProsthesis, total anatomic shoulder, uncemented metaphyseal humeral stem with no diaphyseal incursion, semi-constrained1 report
Recent Tornier Perform adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2026Fracture
Patient problems: Insufficient Information
MAUDE report 50935307 ↗MalfunctionSep 25, 2026Corroded; Fracture
Tip of driver broke off while in use (tightening the glenosphere). Broken tip removed from implant, 5-minute delay of case. No debris reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50898909 ↗MalfunctionSep 17, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50809706 ↗MalfunctionSep 16, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50795943 ↗MalfunctionSep 16, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50795942 ↗MalfunctionSep 9, 2026Crack
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50701503 ↗MalfunctionSep 8, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50675203 ↗MalfunctionJul 29, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50074249 ↗MalfunctionJul 27, 2026Fracture
As reported: "Found tip of driver to be sheared off."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50046410 ↗MalfunctionJul 27, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50046201 ↗MalfunctionJul 27, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50046198 ↗MalfunctionJul 15, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25830016 ↗MalfunctionJul 15, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25829368 ↗MalfunctionJul 15, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25829139 ↗MalfunctionJul 9, 2026Fracture; Material Deformation
Screwdriver bits were warped or broken.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25764165 ↗
Other Tornier, Inc. products
- Tornier Perform Reversed Glenoid41 models · 515 reports · 1 recall
- TORNIER PERFORM HUMERAL SYSTEM68 models · 190 reports · 1 recall
- Tornier HRS40 models · 176 reports · 1 recall
- Tornier Perform Reversed Augmented Glenoid8 models · 121 reports · 1 recall
- AEQUALIS FLEX REVIVE24 models · 70 reports · 2 recalls
- Latitude - Elbow35 models · 147 reports
- Tornier Latitude7 models · 14 reports · 1 recall
- Latitude EV24 models · 56 reports
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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