Howmedica Osteonics Corp. recalls
17 recalls filed under Howmedica Osteonics Corp.. The most recent was published September 23, 2026.
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Class II · last month
Howmedica Osteonics Corp. Axle PIN Assy Large Elbow Cobalt Chrome recall: Affected devices were manufactured with Ultra High Molecular Weight
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the…
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Class II · last month
Howmedica Osteonics Corp. Triathlon Hinge Insert Size 4 11MM 5612-P-411 Triathlon recall: Affected devices were manufactured with Ultra High Molecular Weight
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the…
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Class II · last month
Howmedica Osteonics Corp. Scorpio Recessed Metal Backed Patella 3045-0026 3045-0028 recall: Affected devices were manufactured with Ultra High Molecular Weight
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the…
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Class II · last month
Howmedica Osteonics Corp. Bearing AND Axle Bushing Assy STD Elbow C-M113-1-301 KRH recall: Affected devices were manufactured with Ultra High Molecular Weight
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the…
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Class II · last month
Howmedica Osteonics Corp. Scorpio + Mobile Bearing PCS 78-5-0910 System ONE Bipolar recall: Affected devices were manufactured with Ultra High Molecular Weight
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the…
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Class II · last month
Howmedica Osteonics Corp. Duracon XL Angled TIB INS 11/14MM C-M064-1-300 recall: Affected devices were manufactured with Ultra High Molecular Weight
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the…
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Class II · last month
Howmedica Osteonics Corp. ALL Poly Constrained Insert 54MM 69-2854 NRG Knee CR recall: Affected devices were manufactured with Ultra High Molecular Weight
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the…
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Class II · last month
Howmedica Osteonics Corp. Trident 0¿ Poly Insert 28mm ID 620-00-28D Orthopaedic recall: Affected devices were manufactured with Ultra High Molecular Weight
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the…
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Class II · last month
Howmedica Osteonics Corp. Omnifit Series I Acet. Insert 10¿ 22mm ID recall: Affected devices were manufactured with Ultra High Molecular Weight
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the…
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Class II · last month
Howmedica Osteonics Corp. Acetabular CUP Uhmwpe 61-3258 ALL Poly Constrained Insert recall: Affected devices were manufactured with Ultra High Molecular Weight
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the…
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Class II · last month
Howmedica Osteonics Corp. ABG I Acetabular Insert Hooded 28mm ID X 48mm C-M079-2-801 recall: Affected devices were manufactured with Ultra High Molecular Weight
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the…
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Class II · last month
Howmedica Osteonics Corp. Scorpio C-Dome Patella 73-2710 73-2910 Scorpio U-Dome recall: Affected devices were manufactured with Ultra High Molecular Weight
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the…
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Class II · 4 months ago
Howmedica Osteonics Corp. TRI TS Baseplate Size 4 recall: Stryker has identified that Triathlon Universal Baseplate Size 3 (lot
Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate…
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Class II · 4 months ago
Howmedica Osteonics Corp. TRI TS Baseplate Size 3 recall: Stryker has identified that Triathlon Universal Baseplate Size 3 (lot
Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate…
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Class II · 7 months ago
Howmedica Osteonics Corp. MICS3 Angled Sagittal Saw Attachment recall: A potential issue was identified with the torque strength on the external
A potential issue was identified with the torque strength on the external screws of the MICS3 Angled Sagittal Saw Attachment. These screws, which…
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Class II · 10 months ago
Howmedica Osteonics Corp. The Stryker CranialMask Tracker is a single-use device recall: When the device is activated during surgery
When the device is activated during surgery, the device software issues an error message "Instrument Face Mask (6001385000000) is not valid for this…
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Class II · 1+ years ago
Howmedica Osteonics Corp. 1. Exeter V40 Stem 44MM NO 2, Model/ recall: a potential product mix where the package labeled as Catalog Number
a potential product mix where the package labeled as Catalog Number 0580-1-442, lot A00976, may contain Catalog Number 0580-1-352, lot G8754849, and…
About this page
Howmedica Osteonics Corp. appears here because a federal agency named it as the recalling firm or the brand on the label. A recall is not a judgement about everything the company sells — it covers only the lot codes and models listed in each notice.