Wright EVOLVE TRIAD Plate Cutter, REF 49510120 — FDA record Z-1366-2022

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jun 14, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
Wright EVOLVE TRIAD Plate Cutter, REF 49510120
Reason
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 instructions for use
Classification
Class II
Recalling firm
Wright Medical Technology, Inc.
Quantity
231
Agency-reported status
Ongoing
Source record identifier
Z-1366-2022

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityLot codes: 955401, 1168853, 1349302, 1956936, 2486857

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

Nationwide and PR, and Australia, Canada, Chile, Colombia, Hong Kong, Puerto Rico

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Report date
Jul 20, 2022
Recall initiation date
Jun 14, 2022
Center classification date
Jul 11, 2022

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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