FDAApril 16, 2024device

Stryker Blueprint Software, Catalog #BPUE001.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The software bug allows for case planning with anatomic glenoid Perform / Perform Augmented implants and anatomic humeral Tornier Flex implant configurations that are incompatible and do not have regulatory approval.

What to do

FDA enforcement status: Ongoing

Brands named

tornier s a stornier

UPCs

03700434023114037004340231070370043401506503700434015058

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Stryker Blueprint Software, Catalog #BPUE001. — Recall Details · AllClear