Every recall we track for Tornier S.A.S. — 13 in all — plus the complaints and injury reports the public filed about them.
Tornier recalls Blueprint software version 4.2.1 for surgeons due to incompatibility with older cases. This affects shoulder replacement planning software.
Tornier recalls Blueprint Mixed Reality Glenoid Box Lids (MRUE205) due to software and instrumentation problems affecting shoulder surgery. Affected units were sold from August 2023 to December 2024.
Tornier recalls HoloBlueprint Application (MRUE001) for total shoulder arthroplasty due to software and instrumentation problems affecting use. Affected users should contact Tornier for details.
Tornier recalls Blueprint Mixed Reality Instrument Check Block (MRUE203) due to software and hardware issues affecting use in total shoulder arthroplasty procedures. Affected units were distributed from August 2023 to December 2024.
Tornier recalls Blueprint Mixed Reality Glenoid Pin Guides (MRUE200) due to software and instrument failures affecting shoulder surgery. Affected units sold from Aug 2023 to Dec 2024.
Tornier recalls Blueprint Mixed Reality Box Base (MRUE204) due to software and instrumentation problems affecting shoulder surgery. Affected units were sold from August 2023 to December 2024.
Tornier recalls Blueprint Mixed Reality Instrument Kit (MRUEGLN) for software and instrument issues affecting total shoulder arthroplasty procedures. Affected units sold from Aug 2023 to Dec 2024.
Tornier recalls Blueprint Mixed Reality Depth Stop Pin (MRUE206) for software and instrumentation problems affecting shoulder surgery. All units made through Oct 2024 are affected.
Tornier recalls Blueprint Mixed Reality Glenoid Digitizers (MRUE201) due to software and instrumentation problems affecting shoulder surgery. Affected units were sold from August 2023 to December 2024.
Tornier recalls Blueprint Mixed Reality Coracoid Clamps (MRUE202) due to software and instrumentation problems affecting shoulder surgery. Affected units were sold from August 2023 to December 2024.
Tornier recalls Stry: Blueprint Mixed Reality Glenoid Pin Guide (MRUE200) due to risk of disassembly during surgery, potentially prolonging procedures. Affected units have specific lot numbers.
Tornier recalls Stryker Blueprint Software versions 2.1.4 to 4.0.2 due to incompatible implant configurations that lack regulatory approval. Affected units have specific UDI-DI numbers.
Tornier recalls specific shoulder implant components (Aequalis Pyrocarbon Humeral Heads) due to potential graphite exposure. Affected models include catalog numbers DWH039 to DWH154 with varying diameters and heights. Consumers should check their implant details and contact Tornier for guidance.
