FDA recall record

Tornier S.A.S Stryker Blueprint Software, Catalog #BPUE001 recall — FDA Z-1883-2024

The software bug allows for case planning with anatomic glenoid Perform / Perform Augmented implants and anatomic humeral Tornier Flex implant…

Class IIclassification
Z-1883-2024official record ID
May 29, 2024report date

Recall record at a glance

Official recordZ-1883-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmTornier S.A.S.
Report dateMay 29, 2024
Recall initiation dateApr 16, 2024
LocationMontbonnot St Martin, France

Official product description

Stryker Blueprint Software, Catalog #BPUE001.

Why the product was recalled

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.

Distribution information

US Nationwide distribution in the states of FL, KY, NJ, and WI.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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