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    "id": "/drug-device-alerts/cobalt-chrome-modular-neck-hip-replacements-risk-of-metal-wear-effects-and-revision-surgery-dsi-slash-2026-slash-010",
    "title": "Cobalt-chrome modular neck hip replacements: risk of metal-wear effects and revision surgery (DSI/2026/010)",
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    "id": "Z-0418-2026",
    "title": "Zimmer Biomet Dual Mobility Vivacit-E Highly Crosslinked Polyethylene, 28 mm I.D., 44 mm O.D., Size F, Bearing, Model/Catalog Number: 110031012; semi constrained hip prosthesis",
    "date": "2025-09-26",
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    "id": "Z-0227-2026",
    "title": "iNSitu Bipolar Hip System, Bipolar head implant Part ID Description 10-22-0038 Bipolar Head Assembly, Size 38mm 10-22-0040 Bipolar Head Assembly, Size 40mm 10-22-0042 Bipolar Head Assembly, Size 42mm 10-22-0044 Bipolar Head Assembly, Size…",
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    "title": "Profemur Cobalt Chrome Modular Neck Hip Replacements: Higher than anticipated risk of revision surgery, metal-wear effects and component fracture (DSI/2025/005)",
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    "url": "https://www.gov.uk/drug-device-alerts/profemur-cobalt-chrome-modular-neck-hip-replacements-higher-than-anticipated-risk-of-revision-surgery-metal-wear-effects-and-component-fracture-dsi-slash-2025-slash-005",
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    "licenseUrl": "https://www.nationalarchives.gov.uk/doc/open-government-licence/version/3/"
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    "id": "Z-2147-2025",
    "title": "Brand Name: EMPOWR Dual Mobility\" Product Name: EMPOWR Acetabular, Dual Mobility, Poly Bearing, ID28, OD40 Model/Catalog Number: 952-28-40E Software Version: NA Product Description: The EMPOWR Dual Mobility\" system is compatible with the…",
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    "source": "FDA",
    "id": "Z-1569-2025",
    "title": "restor3d Cordera Hip System. ACETABULAR LINER GRP C 36MM LIP. Model Number: HDL-060-C22L-000101 Acetabular Liner for Cordera Hip System",
    "date": "2025-03-25",
    "url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=213239",
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    "procedureSlug": "knee-replacement",
    "source": "FDA",
    "id": "Z-3197-2026",
    "title": "ALL POLY CONSTRAINED INSERT 54MM 69-2854 NRG KNEE CR 82-2-0512 82-2-0518 82-2-0912 NRG KNEE P/S 82-3-0318 SCORPIO + MOBILE BEARING PCS 78-5-0910 SCORPIO C-DOME PATELLA 73-2710 SCORPIO INSET PATELLA 73-2610 SCORPIO M-DOME PATELLA 73-0110…",
    "date": "2026-07-30",
    "url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=221971",
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    "procedureSlug": "knee-replacement",
    "source": "FDA",
    "id": "Z-2617-2026",
    "title": "Depuy Synthes, ATTUNE Revision Hinge Knee Hinge Insert Components with the below product descriptions and Part Codes. 1. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 4 10mm B; Part Number: 151730410. 2. ATTUNE KNEE SYSTEM REVISION HINGE…",
    "date": "2026-05-19",
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    "source": "FDA",
    "id": "Z-2897-2026",
    "title": "Brand Name: U2 Total Knee System Product Name: Femoral offset bushing, 0mm and 4mm Model/Catalog Number: 9323-5310 Software Version: N/A Product Description: Manual Orthopedic Surgical Instrument Component: No, N/A",
    "date": "2026-03-19",
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    "source": "FDA",
    "id": "Z-2700-2026",
    "title": "Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Model/Catalog Number: 342-19-703 Product Description: Enovis knee devices are intended for knee arthroplasty.",
    "date": "2026-02-16",
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    "source": "MHRA",
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    "title": "Symbios ORIGIN® Posterior Stabilised Patient-Matched Total Knee Replacement Device: Risk of Early Revision, DSI/2024/005",
    "date": "2024-04-23",
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    "licenseUrl": "https://www.nationalarchives.gov.uk/doc/open-government-licence/version/3/"
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  {
    "procedureSlug": "knee-replacement",
    "source": "MHRA",
    "id": "/drug-device-alerts/nexgen-knee-replacement-affected-patients-should-be-offered-additional-follow-up",
    "title": "NexGen Knee replacement: affected patients should be offered additional follow up, DSI/2023/003",
    "date": "2023-02-15",
    "url": "https://www.gov.uk/drug-device-alerts/nexgen-knee-replacement-affected-patients-should-be-offered-additional-follow-up",
    "license": "Open Government Licence v3.0",
    "licenseUrl": "https://www.nationalarchives.gov.uk/doc/open-government-licence/version/3/"
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  {
    "procedureSlug": "shoulder-replacement",
    "source": "FDA",
    "id": "Z-3200-2026",
    "title": "DURACON XL ANGLED TIB INS 11/14MM C-M064-1-300 SELF-PRESSURIZING GLENOID SIZE 8 C-M062-6-800 C-M062-7-500 C-M063-2-600 SELF-PRESSURIZING GLENOID SIZE 9 C-M063-5-000 SHOULDER - GLENOID #11 5361-6111 SHOULDER - GLENOID #5 5361-6105 SHOULDER…",
    "date": "2026-07-30",
    "url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=221975",
    "license": "Public domain",
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  {
    "procedureSlug": "shoulder-replacement",
    "source": "FDA",
    "id": "Z-2987-2026",
    "title": "Brand Name: Veritas Standard Reverse Total Shoulder Product Name: Veritas Standard Glenoid Baseplate Model/Catalog Number: 1500-1030; 1500-1035 Software Version: N/A - off-the-shelf hardware product Product Description: The restor3d…",
    "date": "2026-06-30",
    "url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=221495",
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  },
  {
    "procedureSlug": "shoulder-replacement",
    "source": "FDA",
    "id": "Z-1458-2026",
    "title": "Brand Name: Reverse Shoulder Prosthesis (RSP) Product Name: RSP HUMERAL SOCKET INSERT, 32MM +4MM, STANDARD HXe-plus Model/Catalog Number: 509-00-432",
    "date": "2026-01-15",
    "url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=218376",
    "license": "Public domain",
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  {
    "procedureSlug": "shoulder-replacement",
    "source": "FDA",
    "id": "Z-2562-2025",
    "title": "Exactech Equinoxe, Reverse Shoulder Humeral Liners, 322-38-00 (145-DEG PE 38MM HUM LINER +0), REF: 322-38-03 (145-DEG PE 38MM HUM LINER +2.5), REF:322-42-00 (145-DEG PE 42MM HUM LINER +0), REF: 322-42-03 (145-DEG PE 42MM HUM LINER +2.5)",
    "date": "2025-08-15",
    "url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=215713",
    "license": "Public domain",
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  },
  {
    "procedureSlug": "shoulder-replacement",
    "source": "FDA",
    "id": "Z-2549-2025",
    "title": "Brand Name: DJO SURGICAL Product Name: FA S Altivate Reverse Glenoid Tray Model/Catalog Number: None Software Version: NA Product Description: Enovis\" shoulder devices are intended for treatment of patients who are candidates for shoulder…",
    "date": "2025-07-18",
    "url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=215551",
    "license": "Public domain",
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  },
  {
    "procedureSlug": "shoulder-replacement",
    "source": "FDA",
    "id": "Z-2008-2025",
    "title": "Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW, 26mm Model/Catalog Number: 506-04-126 Software Version: NA Product Description: Encore Medical L.P. shoulder devices are intended for treatment of patients…",
    "date": "2025-05-28",
    "url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=214024",
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  {
    "procedureSlug": "disc-replacement",
    "source": "FDA",
    "id": "Z-2050-2026",
    "title": "Prodisc C SK U.S. IMPLANT EXTRA LARGE 5MM. Model: PDSXL5 Total cervical disc replacement.",
    "date": "2026-03-20",
    "url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=219561",
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  {
    "procedureSlug": "disc-replacement",
    "source": "MHRA",
    "id": "/drug-device-alerts/m6-c-artificial-cervical-disc-spinal-kinetics-llc-new-monitoring-requirements-for-the-risk-of-osteolysis",
    "title": "M6-C Artificial Cervical Disc, Spinal Kinetics LLC: New monitoring requirements for the risk of osteolysis (DSI/2026/001)",
    "date": "2026-01-15",
    "url": "https://www.gov.uk/drug-device-alerts/m6-c-artificial-cervical-disc-spinal-kinetics-llc-new-monitoring-requirements-for-the-risk-of-osteolysis",
    "license": "Open Government Licence v3.0",
    "licenseUrl": "https://www.nationalarchives.gov.uk/doc/open-government-licence/version/3/"
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  {
    "procedureSlug": "disc-replacement",
    "source": "FDA",
    "id": "Z-1426-2026",
    "title": "Brand Name: Prodisc Product Name: Prodisc C SK Model/Catalog Number: PDSL6 Software Version: N/A Product Description: Total cervical disc replacement Component: No",
    "date": "2025-12-31",
    "url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=218137",
    "license": "Public domain",
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  },
  {
    "procedureSlug": "disc-replacement",
    "source": "FDA",
    "id": "Z-3212-2024",
    "title": "prodisc C SK, Total cervical disc replacement, medical device, Model/Catalog Number: PDSM5",
    "date": "2024-07-18",
    "url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=209638",
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  {
    "procedureSlug": "disc-replacement",
    "source": "FDA",
    "id": "Z-1453-2022",
    "title": "Description/Part: Simplify Disc Size 1, Ht 5/SM-5; Simplify Disc Size 1, Ht 6/SM-6; Simplify Disc Size 2, Ht 4/MD-4; Simplify Disc Size 2, Ht 5/MD-5; Simplify Disc Size 2, Ht 5, 5/MD-5L; Simplify Disc Size 2, Ht 6/MD-6; Simplify Disc Size…",
    "date": "2022-06-20",
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    "license": "Public domain",
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    "procedureSlug": "spinal-fusion",
    "source": "FDA",
    "id": "Z-0478-2026",
    "title": "Virata Preassembled Polyaxial Screw, utilized in the Virata Spinal Fixation System. The following sizes are affected: 1. POLYAXIAL SCREW, CC, 5.5mm X 30mm; Item Number: TL1-10755030. 2. POLYAXIAL SCREW, CC, 5.5mm X 35mm; Item Number:…",
    "date": "2025-09-19",
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    "source": "FDA",
    "id": "Z-1065-2025",
    "title": "Calibrate CCX Interbody System for spinal fusion procedures: Implants: (1) Calibrate CCX-O, 7 x 10 x 25mm 5 degrees, Part #325-07102505, nonsterile; (2) Calibrate CCX-O, 7 x 10 x 25mm 10 degrees, Part #325-07102510, nonsterile; (3)…",
    "date": "2024-12-15",
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    "id": "Z-0125-2025",
    "title": "Cortera Spinal Fixation System Screw, Poly, Solid, 6.5mm x 45mm, REF: 150100-65045",
    "date": "2024-08-21",
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    "id": "Z-0846-2024",
    "title": "Cortera Spinal Fixation System, REF: 150100-85050. Spinal fixation screws labeled as 8.5 mm diameter, 50 mm length.",
    "date": "2023-11-28",
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    "id": "Z-0639-2024",
    "title": "Vitality Polyaxial Screw, 7.5mmx 50mm, REF: 07.02000.118, used with Vitality and Vital Spinal Fixation System",
    "date": "2023-10-16",
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    "id": "Z-2121-2023",
    "title": "Medtronic Catalyft LS Expandable Interbody System, Anterior Standalone Cage, REF 981027722, spinal implant",
    "date": "2023-06-06",
    "url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=201711",
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    "source": "FDA",
    "id": "Z-2929-2026",
    "title": "GM Helix Implant, Endosseous Dental Implant Article No. 109.984",
    "date": "2026-07-13",
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    "source": "FDA",
    "id": "Z-1995-2026",
    "title": "Straumann n!ce Zr, HT, Full-arch Restoration. Article 010.0158. Endosseous Dental Implant Abutments",
    "date": "2026-03-27",
    "url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=219528",
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    "source": "FDA",
    "id": "Z-1671-2025",
    "title": "WB XL Anatomic Healing Abutment XC. Endosseous Dental Implant Abutments.",
    "date": "2025-04-17",
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    "id": "Z-1273-2025",
    "title": "ET Rigid Abutment (Mini) SIze: 4.5D 4.0G/H 4.0H - Intended for use with a dental implant to provide support for prosthetic restorations such as crowns, bridges, or overdentures. Model/Catalog Number: ETRGA4544MP",
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    "source": "FDA",
    "id": "Z-1101-2025",
    "title": ". Nobel Biocare N1 TiUltra TCC RP 4.0x9mm . Nobel Biocare N1 TiUltra TCC RP 4.0x11mm . Nobel Biocare N1 TiUltra TCC RP 4.0x13mm Nobel Biocare N1 TiUltra TCC implants are intended for use as an endosseous dental implant in the maxilla or…",
    "date": "2025-01-10",
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    "id": "Z-2318-2024",
    "title": "9006767 Astra EV 4.8mm Milled Titanium Abutment Milled abutments are too be used in conjunction with an endosseous dental implant fixture to aid in prosthetic rehabilitation.",
    "date": "2024-04-10",
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    "id": "Z-2929-2026",
    "title": "GM Helix Implant, Endosseous Dental Implant Article No. 109.984",
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    "title": "Straumann n!ce Zr, HT, Full-arch Restoration. Article 010.0158. Endosseous Dental Implant Abutments",
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    "id": "Z-1671-2025",
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