Tornier, Inc.
10801 Nesbitt Avenue South, Bloomington, MN, US
Registered product codes
63 product codes
Recent MDR events
3,858 on file
- LATITUDE FLEXIBLE REAMER 5MMJul 31, 2026Malfunction0001649390-2026-00776
- PERFORM REVERSED PERIPHERAL and SPHERE SCREWDRIVER BIT T20Jul 29, 2026Malfunction0001649390-2026-00775
- Unk Simpliciti implantsJul 28, 2026Injury0001649390-2026-00762
- Unk Simpliciti implantsJul 28, 2026Injury0001649390-2026-00766
- Unk Simpliciti implantsJul 28, 2026Injury0001649390-2026-00765
- Unk Simpliciti implantsJul 28, 2026Injury0001649390-2026-00767
- Unk Simpliciti implantsJul 28, 2026Injury0001649390-2026-00769
- Unk Simpliciti implantsJul 28, 2026Injury0001649390-2026-00768
- Unk Simpliciti implantsJul 28, 2026Injury0001649390-2026-00764
- Unk Simpliciti implantsJul 28, 2026Injury0001649390-2026-00763
Recalls
20 on file
- Open, ClassifiedApr 3, 2026
Affected products were incorrectly labeled as Tornier HRS Max products. These parts are compatible with the Tornier HRS system only, and are incompatible with the Tornier HRS Max system.
View FDA record ↗ - Open, ClassifiedFeb 2, 2026
A specific lot of screws is incorrectly labeled. Screws are labeled as 5.0mmx18mm but actual screws are 5.00mmx14mm. If mismatch is detected during surgery, the issue may cause a minor delay in surgery. If not detected and incorrect screw is used, issue may increase risk of earlier mechanical failure, loosening, and need for revision surgery.
View FDA record ↗ - Open, ClassifiedApr 22, 2025
A specific lot of Latitude Humeral Trial Stems has the incorrect direct part marking. " Laser Marked: 9030103, Humeral Stem Trial 150mm Large / Right, Yellow color indicator (incorrect) " Device Actually: 9030092, Humeral Stem Trial 150mm Medium / Left, Red color indicator (correct)
View FDA record ↗ - Open, ClassifiedSep 27, 2024
Devices from one lot of Perform" Reversed Inserts may contain a locking ring that was assembled upside down which would prevent the humeral insert from securely seating in the stem or spacer.
View FDA record ↗ - Open, ClassifiedSep 16, 2024
One lot of Perform Humeral Nucleus may exceed the specification for bacterial endotoxin load (max 20 EU/device).
View FDA record ↗ - Open, ClassifiedJan 19, 2024
The incorrect device is contained in the labeled package.
View FDA record ↗ - Open, ClassifiedOct 13, 2023
One lot of Tournier Perform Reversed Lateralized Baseplates were found to have been manufactured with 6mm spacers instead of 3mm spacers. This nonconformance prevents the central screw from being able to thread into the baseplate.
View FDA record ↗ - Open, ClassifiedJun 28, 2023
A comingle/swap resulted in the labeling and laser marking on the product to state it is a Aequalis Flex Revive Assembly Screw 0mm Standard (ARS655101) but it was a Aequalis Flex Revive Assembly Screw 0mm Short (ARS655118) & vice versa.
View FDA record ↗ - Open, ClassifiedJun 28, 2023
A comingle/swap resulted in the labeling and laser marking on the product to state it is a Aequalis Flex Revive Assembly Screw 0mm Standard (ARS655101) but it was a Aequalis Flex Revive Assembly Screw 0mm Short (ARS655118) & vice versa.
View FDA record ↗ - TerminatedAug 26, 2015
Tornier has initiated a voluntary recall for the Salto Talaris Tibial Guide (part number MJU333) due to a complaint that occurred during physician training, that the guide cannot be assembled to the Salto Talaris Talar Pin Setting guide. This issue will cause the impossibility the time of putting the Talar pin in the guide.
View FDA record ↗
Compliance history
Matched by FEI 3000718467.
FDA inspections
0 on file
No inspections on file for this FEI number.
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.