Tornier, Inc recalls
Every recall we track for Tornier, Inc — 14 in all, from 2018–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
14 recalls since 2017.
All FDA recall records for Tornier, Inc since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 1 | 1 | 0 | 2 |
| 2019 | 0 | 0 | 1 | 0 | 1 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 1 | 0 | 1 |
| 2022 | 0 | 0 | 1 | 0 | 1 |
| 2023 | 0 | 0 | 3 | 0 | 3 |
| 2024 | 0 | 1 | 2 | 0 | 3 |
| 2025 | 0 | 0 | 2 | 0 | 2 |
| 2026 (to date) | 0 | 0 | 1 | 0 | 1 |
What to do if you have a recalled Tornier, Inc product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Tornier, Inc recalls
13 shown- Lower riskMedical device
Tornier, Inc recalls Tornier HRS Max parts: 1. TORNIER HRS Max Tuberosity Body Lat Coat, Small, Cat. No. ARS1041101 2. TORNIER HRS Max
Tornier recalls specific HRS Max parts that are incompatible with the Tornier HRS Max system. These parts may cause system errors if used incorrectly. Affected products include Tuberosity Body Lat Coat and No Coat parts with specific lot numbers.
TornierMar 5, 2026 - Lower riskMedical device
Tornier, Inc recalls TORNIER PERFORM REVERSED PERIP SCREW 5.0MMX18MM NON STERILE, catalog number DWJ318
Tornier recalls specific lot of perip screws (DWJ318, Lot AZ482: 5.0mmx18mm labeled but 5.00mmx14mm actual). Mismatch risks surgery delays or revision surgery. No remedy provided.
TornierDec 19, 2025 - Lower riskMedical device
Tornier, Inc recalls stryker Latitude EV HUMERAL REVISION STEM TRIAL, L: 150mm, Size: LARGE, Side: RIGHT, REF 9030103; Prosthesis, Elbow,
Tornier recalls specific Latitude EV Humeral Revision Stem Trial models with incorrect part markings that could lead to improper fitting. Affected units have a laser marking of 9030103 but are actually 9030092. Consumers should contact Tornier for verification.
TornierMar 3, 2025 - Use cautionMedical device
Tornier, Inc recalls Stryker Tornier Perform Humeral System, Reversed Insert, 45%, REF DWP2393, for shoulder arthroplasty
Stryker Tornier recalls 45% reversed inserts for shoulder surgery due to potential improper assembly causing safety risks. Affected units have specific batch numbers and model identifiers.
TornierAug 29, 2024 - Lower riskMedical device
Tornier, Inc recalls stryker TORNIER PERFORM HUMERAL SYSTEM - STEMLESS US Anatomic Nucleus, REF DWM003A; anatomic total arthroplasty of the
Tornier recalls a specific lot of Perform Humeral Nucleus implants due to potential bacterial endotoxin levels exceeding safety limits. Affected patients should contact Tornier for guidance.
TornierAug 29, 2024 - Lower riskMedical device
Tornier, Inc recalls Stryker Tornier Perform Reversed Glenoid Press-Fit Short Post Ti6AI4V, REF DWJ001, L: 7mm, Cementless Sterile.
Recall of Tornier Stryker Perform Reversed Glenoid Press-Fit Short Post Ti6AI4V (REF DWJ001, L: 7mm) due to incorrect device in labeled package. Affected units include specific batch and serial numbers.
TornierJan 3, 2024 - Lower riskMedical device
Tornier, Inc recalls stryker Tornier Perform Reversed Augmented Glenoid Lateralized Baseplate, 25mm, Offset +3mm, REF DWJ502
Tornier recalls specific 25mm Perform Reversed Augmented Glenoid Lateralized Baseplates with 6mm spacers instead of 3mm, preventing screw threading. Affected units have UDI 10846832062017 and Lot 1756123.
TornierSep 15, 2023 - Lower riskMedical device
Tornier, Inc recalls AEQUALIS FLEX REVIVE Assembly Screw 0mm Short, Model Number ARS655118
Tornier recalls 55 specific AEQUALIS FLEX REVIVE Assembly Screws (model ARS655118) due to labeling error with standard screws. This mix-up could cause incorrect assembly in medical devices.
TornierJun 12, 2023 - Lower riskMedical device
Tornier, Inc recalls Ratcheting Screwdriver Handle, provided in the Aequalis Perform Reversed kit
Tornier recalls ratcheting screwdriver handles from Aequalis Perform Reversed kit (model MWJ128) due to failure to meet sterilization standards in Aesculap containers. Affected units must be checked for lot codes.
TornierMay 3, 2022 - Lower riskMedical device
Tornier, Inc recalls Aequalis Ascend Flex Shoulder System Reversed Platform (Reversed Tray component) Rx Only Sterile Manufacturer Tornier
Tornier recalls specific lots of Aequalis Ascend Flex Shoulder System Reversed Tray components due to incorrect thickness. Affected patients should contact Tornier for guidance.
TornierMay 28, 2021 - Lower riskMedical device
Tornier, Inc recalls Aequalis Ascend Flex Humeral Stem: Part Number UDI DWF601A 3700386944475 DWF601B 3700386944482 DWF601C 3700386944499
Tornier recalls Aequalis Ascend Flex humeral stems with specific part numbers due to potential movement in shipping packaging that could transfer PETG material to the stem.
TornierOct 18, 2019 - Use cautionMedical device
Tornier, Inc recalls AEQUALIS HUMERAL NAIL DRILL BIT, REF 7020140 Product Usage: The Aequalis Humeral Nail system is intended to provide
Tornier recalls AEQUALIS Humeral Nail Drill Bits (ref 7020140) with defective tips that may puncture sterile packaging, risking infection during surgery. Affected lot numbers listed.
TornierMar 26, 2018 - Lower riskMedical device
Tornier, Inc recalls Fornier Phantom Fiber(TM) Sutures: Item Number Description SMB000425 4.5 MM PHANTOM FT BIOCOMPOSITE SUTURE ANCHOR WITH
Tornier recalls Phantom Fiber sutures that may lose strength faster if improperly stored, potentially affecting surgical safety. Affected items include specific sizes and packaging. Consumers should check product details and contact Tornier for guidance.
TornierFeb 8, 2018
Tornier, Inc recall questions
How many recalls has Tornier, Inc had?
14 recalls from Tornier, Inc are on record with U.S. safety agencies, from 2018–2026.
What is the most recent Tornier, Inc recall?
Tornier, Inc recalls Tornier HRS Max parts: 1. TORNIER HRS Max Tuberosity Body Lat Coat, Small, Cat. No. ARS1041101 2. TORNIER HRS Max, dated Mar 5, 2026. Every Tornier, Inc recall is listed on this page, newest first.
What should I do if I have a recalled Tornier, Inc product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Tornier, Inc recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.