Medacta Usa recalls
Medacta Usa has 20 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 8 Jul 2026. 1 is still ongoing. 1 was reported in the last 12 months. The most frequent reason is device malfunction.
Total recalls 20 since 2012
Last 12 months 1 reported
Class I 0 0% of total
Ongoing 1 latest 8 Jul 2026
Recalls per month, last 24 months click a bar for that month Severity split
0 0%20 100%0 0%
Why medacta usa is recalled
Ongoing medacta usa recalls 1 active
All medacta usa recalls, newest first 20 total Reported Class Recall Company Reason Where 8 Jul 2026 Device CLASS II Short Monobloc Stem Broaches, Size recalled by Medacta Usa Medacta Usa Device Malfunction Nationwide 26 Apr 2023 Device CLASS II MectaLIF Anterior - Lag Plate Flush H16 recalled by Medacta Usa Medacta Usa Device Malfunction 5 states 26 Apr 2023 Device CLASS II MectaLIF Anterior - Lag Plate Flush H12 recalled by Medacta Usa Medacta Usa Device Malfunction 5 states 26 Apr 2023 Device CLASS II MectaLIF Anterior - Lag Plate Flush H18 recalled by Medacta Usa Medacta Usa Device Malfunction 5 states 26 Apr 2023 Device CLASS II MectaLIF Anterior - Antibackout Lag Cover recalled by Medacta Usa Medacta Usa Device Malfunction 5 states 26 Apr 2023 Device CLASS II MectaLIF Anterior - Lag Plate Flush H14 recalled by Medacta Usa Medacta Usa Device Malfunction 5 states 26 Apr 2023 Device CLASS II MectaLIF Anterior - Lag Plate Flush H10 recalled by Medacta Usa Medacta Usa Device Malfunction 5 states 14 Dec 2022 Device CLASS II NextAR Shoulder Surgical Technique recalled by Medacta Usa Medacta Usa Potency & Assay 7 states 15 Jun 2022 Device CLASS II GMK Efficiency - GMK Sphere CR Insert Instrument Set Size recalled Medacta Usa Other 7 states 15 Jan 2020 Device CLASS II Medacta Shoulder System Humeral Anatomical Metaphysis recalled Medacta Usa Other Nationwide 31 Oct 2018 Device CLASS II Medacta International MiniMAX Cementless Anatomical Stem recalled Medacta Usa Packaging Defects ID, NC 27 Dec 2017 Device CLASS II The GMK knee system: designed for cemented use recalled by Medacta Usa Medacta Usa Other Nationwide 12 Jul 2017 Device CLASS II Medacta Gmk Hinge, Tibial Insert Fixed, Size 2, Height recalled Medacta Usa Device Malfunction AZ, CA, NC 25 Jan 2017 Device CLASS II Medacta International SA, M.U.S.T recalled Medacta Usa Sterility Nationwide 25 Nov 2015 Device CLASS II GMK Hinge knee prosthesis recalled by Medacta U Medacta Usa Packaging Defects IL, OH, UT 26 Nov 2014 Device CLASS II The MectaLIF Oblique Handle recalled by Medacta U Medacta Usa Other CA, CO, ID 19 Nov 2014 Device CLASS II GMK Intramedullary Extension Rod is a rod to obtain correct recalled Medacta Usa Device Malfunction IL 6 Mar 2013 Device CLASS II Versafitcup Impacting Ring recalled by Medacta Usa Medacta Usa Device Malfunction Nationwide 13 Feb 2013 Device CLASS II Medacta Quadra Trial Broach size 0 part # recalled Medacta Usa Other Nationwide 14 Nov 2012 Device CLASS II Quadra S Offset Broach Handle The offset broach handle recalled Medacta Usa Other CO, NV, TX
About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.