Spinal Implants recalls
1,159 medical device recalls in the spinal implants category are on file with the FDA, from 2012 to 30 Sep 2026.
Total recalls 1,159 since 2012
Last 12 months 62 reported
Class I 71 6% of total
Ongoing 248 latest 30 Sep 2026
Recalls per month, last 24 months click a bar for that month
Severity split
Class I 71 6% Class II 1,047 90% Class III 41 4%
Why spinal implants is recalled
Ongoing spinal implants recalls 248 active
All spinal implants recalls, newest first 1,159 total
Reported Class Recall Company Reason Where 30 Sep 2026 Device CLASS II Extended Polyaxial Head, Attached Gimbal recalled Seaspine Orthopedics Other Nationwide 30 Sep 2026 Device CLASS II Medline Convenience Kits: Anterior Spine Pack recalled Medline Industries Other Nationwide 9 Sep 2026 Device CLASS II Neuro; Neuro; Crani; Ortho Spine Pack; Bmhm Neuro Pack recalled Avid Medical Sterility Nationwide 9 Sep 2026 Device CLASS II Halyard medical convenience kits labeled as: ENT recalled Avid Medical Sterility Nationwide 9 Sep 2026 Device CLASS II Halyard medical convenience kits labeled as: A-P PACK recalled Avid Medical Sterility Nationwide 2 Sep 2026 Device CLASS II Medline medical convenience kits, labeled as recalled Medline Industries Other Nationwide 2 Sep 2026 Device CLASS II Medline medical convenience kits, labeled as recalled Medline Industries Other Nationwide 26 Aug 2026 Device CLASS II medical procedure kits and trays labeled as: Crani Pack recalled American Contract Systems Sterility IA, MN, MO 26 Aug 2026 Device CLASS II medical procedure kits and trays labeled as recalled American Contract Systems Sterility IA, MN, MO 19 Aug 2026 Device CLASS II Cardinal Health Presource Kits: Basic Pack recalled Cardinal Health 200 Other Nationwide 19 Aug 2026 Device CLASS II Cardinal Health Presource Kits: Septo Rhino Pack recalled Cardinal Health 200 Other Nationwide 19 Aug 2026 Device CLASS II Cardinal Health Presource Kits: Harmonized Spine Vch Phc Pack recalled Cardinal Health 200 Other Nationwide 12 Aug 2026 Device CLASS I Infinion Cx Lead Kit recalled by Boston Scientific Boston Scientific Neuromodulation Other NY 12 Aug 2026 Device CLASS II Anti-Torque, Vector, Part: LS-749 part of Vector Pedicle recalled Innovasis Other Nationwide 5 Aug 2026 Device CLASS II Ams Aligned Medical Solutions medical convenience kits recalled Windstone Medical Packaging Sterility Nationwide 5 Aug 2026 Device CLASS II Ams Aligned Medical Solutions medical convenience kits recalled Windstone Medical Packaging Packaging Defects Nationwide 5 Aug 2026 Device CLASS II Ams Aligned Medical Solutions medical convenience kits recalled Windstone Medical Packaging Sterility Nationwide 5 Aug 2026 Device CLASS II Ams Aligned Medical Solutions medical convenience kits recalled Windstone Medical Packaging Sterility Nationwide 5 Aug 2026 Device CLASS II OsteoBallast, . (SeaSpine Brand) recalled by IsoTis OrthoBiologics SeaSpine IsoTis OrthoBiologics Other Nationwide 29 Jul 2026 Device CLASS II SeaSpine Polyaxial Head recalled by Seaspine Orthopedics Seaspine Orthopedics Other Nationwide 29 Jul 2026 Device CLASS II Medline medical convenience kits labeled as recalled Medline Industries Other 10 states 8 Jul 2026 Device CLASS II Pilling Wecksorb Neurosponges recalled by Teleflex Teleflex Device Malfunction Nationwide 1 Jul 2026 Device CLASS II Convenience kits containing select SKUs of Polycarbonate recalled Medline Industries Other Nationwide 24 Jun 2026 Device CLASS I Description/REF: Spinal Anesthesia KIT/Asa-24090-SB; Spinal recalled Arrow International Sterility Nationwide 10 Jun 2026 Device CLASS I Design Options Spinal Tray Spinal Needle Anesthesia recalled B Braun Medical Processing Deviation Nationwide 10 Jun 2026 Device CLASS I BD¿Spinal Tray with BD¿Whitacre Needle recalled by Becton Dickinson & Becton Dickinson Processing Deviation Nationwide 10 Jun 2026 Device CLASS II Lyndon B Johnson Hospital Spinal Epid recalled by B Braun Medical B Braun Medical Device Malfunction Nationwide 10 Jun 2026 Device CLASS I BD¿Spinal Tray with BD¿Whitacre Needle recalled by Becton Dickinson & Becton Dickinson Processing Deviation Nationwide 10 Jun 2026 Device CLASS I BD¿Spinal Tray with BD¿Quincke Needle recalled by Becton Dickinson & Becton Dickinson Processing Deviation Nationwide 10 Jun 2026 Device CLASS I BD¿Spinal Tray with BD¿Whitacre Needle recalled by Becton Dickinson & Becton Dickinson Processing Deviation Nationwide
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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.