SEASPINE ORTHOPEDICS CORPORATION recalls
Every recall we track for SEASPINE ORTHOPEDICS CORPORATION — 11 in all, from 2024–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from SEASPINE ORTHOPEDICS CORPORATION fell by more than half in 2025 (2, down from 7 in 2024).
All FDA recall records for SEASPINE ORTHOPEDICS CORPORATION 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 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 2 | 2 | 3 | 7 |
| 2025 | 0 | 1 | 1 | 0 | 2 |
| 2026 (to date) | 0 | 1 | 0 | 1 | 2 |
What to do if you have a recalled SEASPINE ORTHOPEDICS CORPORATION 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 SEASPINE ORTHOPEDICS CORPORATION recalls
9 shown- UnratedMedical device
SEASPINE ORTHOPEDICS CORPORATION recalls SeaSpine Mariner Deformity Product Name: Extended Polyaxial Head, Attached Gimbal, 12mm REF: MD1-300010-12
SeaSpine recalls specific Mariner Deformity products due to proximal thread depth being out of design specs. Affected units include model MD1-300010-12 with certain lot numbers. No remedy provided in official notice.
SeaSpineAug 19, 2026 - Use cautionMedical device
SEASPINE ORTHOPEDICS CORPORATION recalls SeaSpine Polyaxial Head REF Number: 41-3010
SeaSpine recalls polyaxial heads with REF 41-3010 due to potential pop-off during surgery. Affected lots include AW199682G and AW199684G. Contact for replacement.
SeaSpineMay 28, 2026 - Lower riskMedical device
SEASPINE ORTHOPEDICS CORPORATION recalls Orthofix NorthStar OCT Navigation Surgical Technique Guide, and instruments: Navigation Driver, REF: PC2-400012;
SEASPINE recalls NorthStar OCT Navigation Surgical Technique Guide and instruments due to incorrect compatibility warnings with Medtronic systems. This could lead to improper use if the guide lists Infinity toolcards as compatible.
SEASPINE ORTHOPEDICSNov 17, 2025 - Use cautionMedical device
SEASPINE ORTHOPEDICS CORPORATION recalls Reef TA Inserter, Part Number: TA2-001003, part of the Reef Interbody System
SEASPINE recalls Reef TA Inserter (Part TA2-001003) due to potential improper implant positioning during spinal surgery. Affected units have specific UDI-DI markings and lot numbers.
SEASPINEAug 6, 2025 - Lower riskMedical device
SEASPINE ORTHOPEDICS CORPORATION recalls Brand Name: Daytona Small Stature Product Name: CoCr LockingCap 4.5mm, Small Stature, T25, BT Model/Catalog Number:
SEASPINE ORTHOPEDICS CORPORATION recalls Daytona Small Stature CoCr LockingCap 4:5mm models with manufacturing defects that may prevent proper component mating. Affected units include specific lot numbers and model 79-0002.
DaytonaOct 29, 2024 - Use cautionMedical device
SEASPINE ORTHOPEDICS CORPORATION recalls Brand Name: Meridian Angled Awl Fixed Product Name: Angled Awl Fixed Model/Catalog Number: RA2-003015 Product
SEASPINE ORTHOPEDICS CORPORATION recalls Meridian Angled Awl Fixed (model RA2-003015) due to insufficient weld around cap component, which may fail under impact forces.
MeridianJun 4, 2024 - UnratedMedical device
SEASPINE ORTHOPEDICS CORPORATION recalls Brand Name: Fathom Pedicle-Based Retractor Product Name: C/C Blade, 50-80mm Model/Catalog Number: MR2102050 Product
SEASPINE ORTHOPEDICS CORPORATION recalls Fathom C/C Blades (model MR2102050) due to potential bone fractures from manufacturing defects. Affected units were sold with lot number WT36299C.
FathomMay 17, 2024 - Use cautionMedical device
SEASPINE ORTHOPEDICS CORPORATION recalls Mariner RDX MIS Polyaxial Head, REF: MX1-001010, part of Mariner RDX MIS Alpha Instruments and Implants, REF: AMRDXMIS,
SEASPINE recalls Mariner RDX MIS Polyaxial Heads (REF MX1-00101: 10889981298647) with partial thread risk causing cross-threading during surgery. Affected units include specific model lots and serial numbers.
SEASPINEFeb 28, 2024 - UnratedMedical device
SEASPINE ORTHOPEDICS CORPORATION recalls Mariner RDX Polyaxial Head, REF: MX1-000020; Mariner RDX Extended Polyaxial Head, REF: MX1-000030; Mariner RDX
SEASPINE recalls specific pedicle screw models due to thin thread design that may cause cross-threading during surgery, potentially leading to complications. Affected models include Mariner RDX Polyaxial and Extended Polyaxial Heads with reference numbers MX1-000020 to MX1-000070.
SEASPINEFeb 15, 2024
SEASPINE ORTHOPEDICS CORPORATION recall questions
How many recalls has SEASPINE ORTHOPEDICS CORPORATION had?
11 recalls from SEASPINE ORTHOPEDICS CORPORATION are on record with U.S. safety agencies, from 2024–2026.
What is the most recent SEASPINE ORTHOPEDICS CORPORATION recall?
SEASPINE ORTHOPEDICS CORPORATION recalls SeaSpine Mariner Deformity Product Name: Extended Polyaxial Head, Attached Gimbal, 12mm REF: MD1-300010-12, dated Aug 19, 2026. Every SEASPINE ORTHOPEDICS CORPORATION recall is listed on this page, newest first.
What should I do if I have a recalled SEASPINE ORTHOPEDICS CORPORATION 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 SEASPINE ORTHOPEDICS CORPORATION 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.