Overview of recall records associated with Wright Medical Technology, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 27.
Screws, intended for use with polyaxial compression plating system intended for foot osteotomies, was manufactured with missing threads on the screwheads, which if used would prevent a…
Stryker has identified an issue that impacts specific lots of Infinity" Resection Guide Adjustment Blocks. The parts within these three lots were found to have been missing an internal…
The devices were manufactured with the pin sleeve holes too narrow, which does not allow the pin sleeves to pass through the pin sleeve holes, thereby preventing pin placement through the…
Stryker has identified an issue that impacts two specific lots of CLAW" II plates. The plates within these two lots were found to have been comingled, resulting in the incorrect product in…
Stryker has identified an issue that impacts two specific lots of CLAW" II plates. The plates within these two lots were found to have been comingled, resulting in the incorrect product in…
The outer label does not match the device inside the package. The affected lot of EVOLVE Proline Stem 7.5mm +2 contains a size 9.5mm +4 stem, while the affected lot of EVOLVE Proline Stem…
The outer label does not match the device inside the package. The affected lot of EVOLVE Proline Stem 7.5mm +2 contains a size 9.5mm +4 stem, while the affected lot of EVOLVE Proline Stem…
An incorrect sizing label was applied to the carton packaging.
The plate cutter is unable to meet sterilization requirements when it is sterilized in a double-wrapped configuration according to the Option 1 Steam Sterilization parameters detailed in…
The instrument is incorrectly color coded.
An incorrect screw is packaged in the product, which contains a locking screw instead of a non-locking screw.
Product was labelled with the incorrect manufacturing and distribution dates.
Incorrect product is contained in the packaging.
Hardware removal kit does not include drivers to remove Dart-Fire 2.5 and 3.0mm Headless screws.
Hardware removal kit does not include drivers to remove Dart-Fire 2.5 and 3.0mm Headless screws.
One lot of INBONE Tibial Trays is missing the plasma coating.
The firm discovered a lack of adequate documentation confirming sterility on certain products.
The firm discovered a lack of adequate documentation confirming sterility on certain products.
The firm discovered a lack of adequate documentation confirming sterility on certain products.
The firm discovered a lack of adequate documentation confirming sterility on certain products.
The firm discovered a lack of adequate documentation confirming sterility on certain products.
These screws have a potential of passing through the plate in the case when torque is applied in excessive amounts, which may result in intraoperative malfunction.
These screws have a potential of passing through the plate in the case when torque is applied in excessive amounts, which may result in intraoperative malfunction.
The term DORSAL was laser etched on the incorrect side on some of the angled handles.
This page summarizes recall records in which the official source identifies Wright Medical Technology, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
