Howmedica Osteonics recalls

Howmedica Osteonics has 248 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 21 Oct 2026. 126 are still ongoing. 20 were reported in the last 12 months.

Total recalls248since 2016
Last 12 months20reported
Class I00% of total
Ongoing126latest 21 Oct 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 246 99%Class III 2 1%

Why howmedica osteonics is recalled

By year

Ongoing howmedica osteonics recalls

126 active

All howmedica osteonics recalls, newest first

248 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IITS Misc. Instruments Tray, Triathlon recalled by Howmedica OsteonicsHowmedica OsteonicsSterilityNJ
DeviceCLASS IITS Femoral Prep Tray, Triathlon recalled by Howmedica OsteonicsHowmedica OsteonicsSterilityNJ
DeviceCLASS IITriathlon Hinge Femoral Prep Tray recalled by Howmedica OsteonicsHowmedica OsteonicsSterilityNJ
DeviceCLASS IITS Universal Baseplate Finishing Tray, Triathlon recalledHowmedica OsteonicsSterilityNJ
DeviceCLASS IIAxle Pin Assy Large Elbow Cobalt Chrome recalled by Howmedica OsteonicsHowmedica OsteonicsOtherNationwide
DeviceCLASS IITriathlon Hinge Insert Size 4 5612-p-411 Triathlon Hinge recalledHowmedica OsteonicsOtherNationwide
DeviceCLASS IIScorpio Recessed Metal Backed Patella 3045 recalledHowmedica OsteonicsForeign MaterialNationwide
DeviceCLASS IIBearing And Axle Bushing Assy Std Elbow C-m113-1-301 Krh recalledHowmedica OsteonicsOtherNationwide
DeviceCLASS IIScorpio + Mobile Bearing Pcs 78-5-0910 System One Bipolar recalledHowmedica OsteonicsOtherNationwide
DeviceCLASS IIDuracon XL Angled Tib Ins C-m064-1-300 Self-pressurizing recalledHowmedica OsteonicsOtherNationwide
DeviceCLASS IIAll Poly Constrained Insert 69-2854 Nrg Knee Cr recalledHowmedica OsteonicsOtherNationwide
DeviceCLASS IITrident 0¿ Poly Insert ID 620-00-28D Orthopaedic implant recalledHowmedica OsteonicsOtherNationwide
DeviceCLASS IIOmnifit Series I Acet recalled by Howmedica OsteonicsHowmedica OsteonicsOtherNationwide
DeviceCLASS IIAcetabular Cup Uhmwpe 61-3258 All Poly Constrained Insert recalledHowmedica OsteonicsOtherNationwide
DeviceCLASS IIAbg I Acetabular Insert Hooded Id C-m079-2-801 Arc2f recalledHowmedica OsteonicsOtherNationwide
DeviceCLASS IIScorpio C-dome Patella 73-2710 73-2910 Scorpio U-dome recalledHowmedica OsteonicsOtherNationwide
DeviceCLASS IITri Ts Baseplate Size recalled by Howmedica OsteonicsHowmedica OsteonicsPackaging DefectsNationwide
DeviceCLASS IITri Ts Baseplate Size recalled by Howmedica OsteonicsHowmedica OsteonicsPackaging DefectsNationwide
DeviceCLASS IIMICS3 Angled Sagittal Saw Attachment recalled by Howmedica OsteonicsHowmedica OsteonicsOtherNationwide
DeviceCLASS IIThe Stryker CranialMask Tracker is a single-use device recalledHowmedica OsteonicsDevice MalfunctionNationwide
DeviceCLASS IIExeter V40 Stem No recalled by Howmedica OsteonicsHowmedica OsteonicsPackaging DefectsNJ
DeviceCLASS IITriathlon Universal TS Baseplate Size recalled by Howmedica OsteonicsHowmedica OsteonicsPotency & AssayNationwide
DeviceCLASS IIMako Integrated Cutting System (Mics) Handpiece recalledHowmedica OsteonicsOtherNationwide
DeviceCLASS IICustom Made Device - Gmrs Extension Piece Left recalledHowmedica OsteonicsOtherNJ
DeviceCLASS IIUnitrax Endoprosthesis Head Component recalled by Howmedica OsteonicsHowmedica OsteonicsLabeling ErrorsNationwide
DeviceCLASS IIUnitrax Endoprosthesis Head Component recalled by Howmedica OsteonicsHowmedica OsteonicsLabeling ErrorsNationwide
DeviceCLASS IIUnitrax Endoprosthesis Head Component recalled by Howmedica OsteonicsHowmedica OsteonicsLabeling ErrorsNationwide
DeviceCLASS IIHRIS Storage & Sterilization Case and Tray recalledHowmedica OsteonicsSterilityNationwide
DeviceCLASS IIGray Revision Instrument System Accessory Tray/Case recalledHowmedica OsteonicsSterilityNationwide
DeviceCLASS IITridentii Hemi CLUSTER54E- Indicated for use in primary recalledHowmedica OsteonicsOtherNationwide

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.