Every recall we track for Tornier, Inc — 14 in all — plus the complaints and injury reports the public filed about them.
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.
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.
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.
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.
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.
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.
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.
Tornier recalls 300+ AEQUALIS FLEX REVIVE Assembly Screw 0mm units (model ARS655101) due to mislabeled parts causing confusion with shorter screws.
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.
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.
Tornier recalls specific lots of Aequalis Ascend Flex Shoulder System Reversed Tray components due to incorrect thickness. Affected patients should contact Tornier for guidance.
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.
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.
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.
