← Every firm
Stryker Spine FDA Recalls
9 recalls on file across devices, 0 of them Class I and 6 still open. Matched by name to SYK.
Newest first
Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.
| Product |
|---|
| Monterey AL Implant Inserter; 10/12mm; Catalog 48019100.Class IIFeb 28, 2025Potential for the gold unlock button to separate from the in |
| Monterey AL Implant Inserter; 22mm; Catalog 48019140.Class IIFeb 28, 2025Potential for the gold unlock button to separate from the in |
| Monterey AL Implant Inserter; 14/16mm; Catalog 48019120.Class IIFeb 28, 2025Potential for the gold unlock button to separate from the in |
| Monterey AL Implant Inserter; 18/20mm; Catalog 48019130.Class IIFeb 28, 2025Potential for the gold unlock button to separate from the in |
| AVS Anchor-C Cervical Cage System Instructions For Use (IFU)- eIFU (revision 5)-Indicated for anterior cervical interbodClass IIAug 23, 2024Labeling Correction: Instructions For Use (IFU)-Updated elec |
| LITe Decompression Snake Arm, REF 48080230Class IINov 1, 2023Product arm was manufactured with the incorrect clamp compon |
| Cortoss Bone Augmentation Material 5cc Cartridge, Catalog Number 2101-0005, GTIN 00808232000962Class IIMay 18, 2021The products experienced a 12-hour excursion from the requir |
| Cortoss Bone Augmentation Material 10cc Cartridge, Catalog Number 2101-0010, GTIN 00808232000979Class IIMay 18, 2021The products experienced a 12-hour excursion from the requir |
| Tritanium X TL Instruments - intervertebral fusion device with bone graft, lumbar. Catalogs:TL Inserter (580220100), TL Class IIMar 11, 2021Stryker identified non-conforming instruments that are compo |