Exactech recalls

Exactech has 197 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 18 Mar 2026. 85 are still ongoing. 5 were reported in the last 12 months.

Total recalls197since 2012
Last 12 months5reported
Class I00% of total
Ongoing85latest 18 Mar 2026

Recalls per month, last 24 months

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Severity split

Class I 0 0%Class II 197 100%Class III 0 0%

By year

Ongoing exactech recalls

85 active

All exactech recalls, newest first

197 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIEquinoxe Core Instrument Kit recalled by ExactechExactechOther19 states
DeviceCLASS IIEquinoxe Ergo Modular Impactor Handle recalled by ExactechExactechOther19 states
DeviceCLASS IIEquinoxe Ergo Adjustable Angle rTSA Reamer recalled by ExactechExactechDevice MalfunctionSC
DeviceCLASS IIEquinoxe Ergo Augments Pilot Tip Converter recalled by ExactechExactechDevice MalfunctionSC
DeviceCLASS IIEquinoxe Ergo Adjustable Angle rTSA Reamer recalled by ExactechExactechDevice MalfunctionSC
DeviceCLASS IIEquinoxe, Reverse Shoulder Humeral Liners recalled by ExactechExactechOtherNationwide
DeviceCLASS IIEquinoxe, Reverse Shoulder Humeral Liners recalled by ExactechExactechOtherNationwide
DeviceCLASS II140-22-70 Nv Ehxl Ntl Lnr G00 140-28-50 Nv Ehxlntrl Lnr G0 recalledExactechOther22 states
DeviceCLASS II140-22-70 Nv Ehxl Ntl Lnr G00 140-28-50 Nv Ehxlntrl Lnr G0 recalledExactechOther22 states
DeviceCLASS II140-28-27 Am Ehxl 0¿ Lnr G 140-32-27 Am Ehxl 0¿ Lnr recalledExactechOther22 states
DeviceCLASS IIAcumatch L-Series Bipolar Liner (Bipolar Endoprosthesis-Hip) recalledExactechPackaging DefectsPR
DeviceCLASS IIOptetrak One Peg Patella recalled by ExactechExactechPotency & AssayFL
DeviceCLASS IIOptetrak, Advanced Patella, 3 Peg Implant recalled by ExactechExactechPotency & AssayFL
DeviceCLASS IIOptetrak Three Peg Patella recalled by ExactechExactechPotency & AssayFL
DeviceCLASS IIOptetrak Inset Patella recalled by ExactechExactechPotency & AssayFL
DeviceCLASS IIEquinoxe Glenoid,Posterior Augment, Pegged, 16o, Right recalledExactechPackaging DefectsNationwide
DeviceCLASS IIEquinoxe Glenoid,Posterior Augment, Pegged, 16o, Left recalledExactechPackaging DefectsNationwide
DeviceCLASS IIEquinoxe Reverse Shoulder Humeral Liner, a) + recalled by ExactechExactechPackaging DefectsNationwide
DeviceCLASS IIEquinoxe Glenoid, Posterior Augment,Pegged, Cemented, 8o recalledExactechPackaging DefectsNationwide
DeviceCLASS IIEquinoxe Reverse Shoulder Constrained Humeral Liner: a) + recalledExactechPackaging DefectsNationwide
DeviceCLASS IIEquinoxe Reverse Shoulder Constrained Humeral Liner, a) + recalledExactechPackaging DefectsNationwide
DeviceCLASS IIEquinoxe Glenoid,Keeled, Cemented, Mates recalled by ExactechExactechPackaging DefectsNationwide
DeviceCLASS IIEquinoxe Cage Glenoid,Posterior Augment, Cemented, Left recalledExactechPackaging DefectsNationwide
DeviceCLASS IIEquinoxe Glenoid,Posterior Augment, Pegged, 12o, Left recalledExactechPackaging DefectsNationwide
DeviceCLASS IIEquinoxe Glenoid,Keeled, Cemented, mates recalled by ExactechExactechPackaging DefectsNationwide
DeviceCLASS IIEquinoxe Reverse Shoulder Constrained Humeral Liner: a) + recalledExactechPackaging DefectsNationwide
DeviceCLASS IIEquinoxe Glenoid,Keeled, Cemented, mates recalled by ExactechExactechPackaging DefectsNationwide
DeviceCLASS IIEquinoxe Glenoid,Keeled, Cemented,47, 50, 53 head recalled by ExactechExactechPackaging DefectsNationwide
DeviceCLASS IIEquinoxe Cage Glenoid,Posterior Augment, Cemented, Right recalledExactechPackaging DefectsNationwide
DeviceCLASS IIEquinoxe Humeral Liner recalled by ExactechExactechPackaging DefectsNationwide

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.