Stryker Spine
6 federal recalls on file. We monitor every CPSC, FDA, USDA, and NHTSA notice for Stryker Spine and translate it into plain English — free weekly digest, optional same-day alerts.
- 2025-04-09FDA-DeviceClass IIMonterey AL Implant Inserter; 22mm; Catalog 48019140.
Potential for the gold unlock button to separate from the inserter.
- 2025-04-09FDA-DeviceClass IIMonterey AL Implant Inserter; 18/20mm; Catalog 48019130.
Potential for the gold unlock button to separate from the inserter.
- 2025-04-09FDA-DeviceClass IIMonterey AL Implant Inserter; 14/16mm; Catalog 48019120.
Potential for the gold unlock button to separate from the inserter.
- 2025-04-09FDA-DeviceClass IIMonterey AL Implant Inserter; 10/12mm; Catalog 48019100.
Potential for the gold unlock button to separate from the inserter.
- 2024-10-02FDA-DeviceClass IIAVS Anchor-C Cervical Cage System Instructions For Use (IFU)- eIFU (revision 5)-Indicated for anterior cervical interbody fusion procedures in skeletally mature patients with cervical disc disease at one level from the C2-C3 disc to the C7-T1 disc.
Labeling Correction: Instructions For Use (IFU)-Updated electronic Rev 5, specific language for indications for use for the United States and Canada was inadvertently removed.
- 2023-12-27FDA-DeviceClass IILITe Decompression Snake Arm, REF 48080230
Product arm was manufactured with the incorrect clamp component. As a result, the affected product arm cannot attach to the arm post shaft.
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