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Wright Medical Technology Inc

Complete recall history across all FDA and CPSC categories — 9 total recalls

Wright Medical Technology Inc appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (9)

FDA medical device enforcement actions by Wright Medical Technology Inc

Date Product Reason Class
Dec 3, 2021 Stryker CLAW II ORTHOLOC 3DSi Plate, Hole Qty: 4, 30mm, REF 40240430. The incorrect product is contained in the packaging. Class II
Dec 3, 2021 Stryker DARCO Screw, Locking, Ti6A14V, REF DC2825016, 2.7mm x 16mm. The incorrect product is contained in the packaging. Class II
Nov 4, 2021 INBONE Total Ankle System, INBONE POLY INSERT SZ 2 10mm SULCUS The package contents and package labeling do not match. Class II
Nov 4, 2021 INBONE Total Ankle System, INBONE POLY INSERT SZ 2+ 14mm SULCUS The package contents and package labeling do not match. Class II
Aug 26, 2020 EVOLVE STEM 8.5MM Model # 496S085 Lack of sterility assurance Class II
Apr 9, 2020 WRIGHT INBONE Tibial Tray, Size: 2, Plasma Spray, Left, REF 2000252902 - Prod... One lot of INBONE Tibial Trays is missing the plasma coating. Class II
Sep 5, 2012 Hip Components: INSERT MOBILE "COLLEGIA" TAILLE 58*28, OT22C58, Lot Numbers... There may be inaccuracies on the labeled shelf life on all products packaged ... Class II
Sep 5, 2012 Extremity Components: PROTHESE A EXPANSION COMPLETE D=6 LG 12 MM, Part Numbe... There may be inaccuracies on the labeled shelf life on all products packaged ... Class II
Sep 5, 2012 Knee Components: ROTULE "913" D=32 , Part Number PGA00030, Lot Number X02383... There may be inaccuracies on the labeled shelf life on all products packaged ... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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