Stryker Spine recalls
Every recall we track for Stryker Spine — 10 in all, from 2018–2025 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Stryker Spine more than tripled in 2025 (4, up from 1 in 2024).
All FDA recall records for Stryker Spine since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 1 | 0 | 1 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 1 | 2 | 0 | 3 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 1 | 0 | 1 |
| 2024 | 0 | 0 | 1 | 0 | 1 |
| 2025 | 0 | 1 | 2 | 1 | 4 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
Most common reasons for Stryker Spine recalls
What to do if you have a recalled Stryker Spine product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Stryker Spine recalls
6 shown- UnratedMedical device
Stryker Spine recalls Monterey AL Implant Inserter; 14/16mm; Catalog 48019120.
Stryker Spine recalls Monterey AL Implant Inserter (14/16mm, Catalog 48019120) due to potential gold unlock button separation. Affected units have specific identifiers; contact for remedy.
Stryker SpineFeb 28, 2025 - Lower riskMedical device
Stryker Spine recalls AVS Anchor-C Cervical Cage System Instructions For Use (IFU)- eIFU (revision 5)-Indicated for anterior cervical
Stryker Spine recalls its AVS Anchor-C Cervical Cage System (revision 5) due to a labeling error in instructions for use. This correction affects U.S. and Canadian patients using the device for cervical fusion procedures.
Stryker Sp: SpineAug 23, 2024 - Lower riskMedical device
Stryker Spine recalls LITe Decompression Snake Arm, REF 48080230
Stryker Spine recalls LITe Decompression Snake Arm (REF 48080230) due to incorrect clamp component preventing attachment to arm post shaft. Affected units have UDI-DI GTIN 07613327263909, lot #227764.
Stryker SpineNov 1, 2023 - Lower riskMedical device
Stryker Spine recalls Cortoss Bone Augmentation Material 5cc Cartridge, Catalog Number 2101-0005, GTIN 00808232000962
Stryker recalls Cortoss Bone Augmentation Material 5cc Cartridges (Catalog 2101-0005) due to potential temperature excursion during distribution. Affected units may not meet refrigeration requirements.
Stryker SpineMay 18, 2021 - Use cautionMedical device
Stryker Spine recalls Tritanium X TL Instruments - intervertebral fusion device with bone graft, lumbar. Catalogs:TL Inserter (580220100), TL
Stryker Spine recalls specific lumbar intervertebral fusion instruments due to potential device failure during spinal surgery. Affected items include TL Inserter, Draw Rod, and Syringe Plunger components with UDI codes listed.
Stryker SpineMar 11, 2021 - Lower riskMedical device
Stryker Spine recalls AVS Aria Cage, Catalog Number 48753212 Product Usage: The Stryker Spine AVS¿ ARIA 1M PEEK Spacers are intervertebral
Stryker Spine recalls AVS Aria Cage (Catalog 48753212) due to anterior and posterior markers being on the wrong sides, potentially causing surgical errors. Affected patients should contact Stryker for guidance.
Stryker SpineAug 13, 2018
Stryker Spine recall questions
How many recalls has Stryker Spine had?
10 recalls from Stryker Spine are on record with U.S. safety agencies, from 2018–2025.
What is the most recent Stryker Spine recall?
Stryker Spine recalls Monterey AL Implant Inserter; 14/16mm; Catalog 48019120., dated Feb 28, 2025. Every Stryker Spine recall is listed on this page, newest first.
Why are Stryker Spine products recalled?
The most common reasons on record: Potential for the gold unlock button to separate from the inserter. (4).
What should I do if I have a recalled Stryker Spine product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Stryker Spine recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.