Fresh Recalls

Howmedica Osteonics recalls

14 recent recalls on record for Howmedica Osteonics in connected official government data as of October 22, 2026 at 6:00 PM UTC.

Models with recalls

ABG I ACETABULAR INSERT HOODED 28mm ID X 48mm C-M079-2-801 ARC2F ACETABULAR INSERT 48/50/5 (1)ACETABULAR CUP UHMWPE 61-3258 ALL POLY CONSTRAINED INSERT 44MM 69-2244 ALL POLY CONSTRAINE (1)ALL POLY CONSTRAINED INSERT 54MM 69-2854 NRG KNEE CR 82-2-0512 82-2-0518 82-2-0912 NRG KNE (1)AXLE PIN ASSY LARGE ELBOW COBALT CHROME Catalog No (1)BEARING AND AXLE BUSHING ASSY STD ELBOW C-M113-1-301 KRH REV TIB INS 16mm THK (1)DURACON XL ANGLED TIB INS 11/14MM C-M064-1-300 SELF-PRESSURIZING GLENOID SIZE 8 C-M062-6-8 (1)OMNIFIT SERIES I ACET (1)SCORPIO + MOBILE BEARING PCS 78-5-0910 SYSTEM ONE BIPOLAR 40MM 6074-4022 SYSTEM ONE BIPOLA (1)SCORPIO C-DOME PATELLA 73-2710 73-2910 SCORPIO U-DOME PATELLA 73-3110 73-3508 73-3708 73-3 (1)SCORPIO RECESSED METAL BACKED PATELLA 3045-0026 3045-0028 3045-0030 3045-0032 Orthopaedic (1)TRI TS BASEPLATE SIZE 3 (1)TRI TS BASEPLATE SIZE 4 (1)TRIATHLON HINGE INSERT SIZE 4 11MM 5612-P-411 TRIATHLON HINGE INSERT SIZE 4 13MM 5612-P-41 (1)TRIDENT 0¿ POLY INSERT 28mm ID 620-00-28D Orthopaedic implant components manufactured from (1)

All Howmedica Osteonics recalls

FDA Class II · Medical device · September 23, 2026

SCORPIO C-DOME PATELLA 73-2710 73-2910 SCORPIO U-DOME PATELLA 73-3110 73-3508 73-3708 73-3 recall — Howmedica Osteonics Corp.

Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…

Official ID Z-3206-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

SCORPIO + MOBILE BEARING PCS 78-5-0910 SYSTEM ONE BIPOLAR 40MM 6074-4022 SYSTEM ONE BIPOLA recall — Howmedica Osteonics Corp.

Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…

Official ID Z-3205-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

TRIDENT 0¿ POLY INSERT 28mm ID 620-00-28D Orthopaedic implant components manufactured from recall — Howmedica Osteonics Corp.

Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…

Official ID Z-3204-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

SCORPIO RECESSED METAL BACKED PATELLA 3045-0026 3045-0028 3045-0030 3045-0032 Orthopaedic recall — Howmedica Osteonics Corp.

Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…

Official ID Z-3203-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

BEARING AND AXLE BUSHING ASSY STD ELBOW C-M113-1-301 KRH REV TIB INS 16mm THK recall — Howmedica Osteonics Corp.

Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…

Official ID Z-3202-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

ACETABULAR CUP UHMWPE 61-3258 ALL POLY CONSTRAINED INSERT 44MM 69-2244 ALL POLY CONSTRAINE recall — Howmedica Osteonics Corp.

Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…

Official ID Z-3201-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

DURACON XL ANGLED TIB INS 11/14MM C-M064-1-300 SELF-PRESSURIZING GLENOID SIZE 8 C-M062-6-8 recall — Howmedica Osteonics Corp.

Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…

Official ID Z-3200-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

ABG I ACETABULAR INSERT HOODED 28mm ID X 48mm C-M079-2-801 ARC2F ACETABULAR INSERT 48/50/5 recall — Howmedica Osteonics Corp.

Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…

Official ID Z-3199-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

TRIATHLON HINGE INSERT SIZE 4 11MM 5612-P-411 TRIATHLON HINGE INSERT SIZE 4 13MM 5612-P-41 recall — Howmedica Osteonics Corp.

Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…

Official ID Z-3198-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

ALL POLY CONSTRAINED INSERT 54MM 69-2854 NRG KNEE CR 82-2-0512 82-2-0518 82-2-0912 NRG KNE recall — Howmedica Osteonics Corp.

Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…

Official ID Z-3197-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

OMNIFIT SERIES I ACET recall — Howmedica Osteonics Corp.

Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…

Official ID Z-3196-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

AXLE PIN ASSY LARGE ELBOW COBALT CHROME Catalog No recall — Howmedica Osteonics Corp.

Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…

Official ID Z-3195-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

TRI TS BASEPLATE SIZE 4 recall — Howmedica Osteonics Corp.

Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot TYX7OB), and Triathlon…

Official ID Z-2462-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

TRI TS BASEPLATE SIZE 3 recall — Howmedica Osteonics Corp.

Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot TYX7OB), and Triathlon…

Official ID Z-2461-2026 · Official record ↗

Verify with the official sources:

Found something wrong or missing? Report a data error.

Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.