Mariner 41-7555-2Recalls & reported problems
Seaspine Orthopedics Corporation · Cannulated Screw 7.50 x 55mm · Class 2 · Implant
All models of Mariner (15)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10889981069025), received between Sep 19, 2024 and Sep 19, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Migration” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Migration1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 19, 2024Migration; Migration
ON (B)(6) 2024, IT WAS OBSERVED VIA X-RAY THAT THERE WAS A POTENTIAL LOOSENING/MIGRATION OF A MARINER MIS ROD IN A PATIENT. THE SURGEON SCHEDULED A REVISION SURGERY ON (B)(6) 2024. CUSTOMER REPORTS PATIENT IS ASYMPTOMATIC AND THERE WAS NO ALLEGED PATIENT INJURY. ALTHOUGH REQUESTED, NO FURTHER INFORMATION WAS PROVIDED. SEE MDR 3012120772-2024-0068 FOR PN MM1-155035, 3012120772-2024-00085 FOR ONE OF THE RETURNED PN MD1-100016, 3012120772-2024-00086 FOR PN MM1-000020,AND 3012120772-2024-00088 FOR THE SECOND RETURNED PN MD1-100016.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20258335 ↗
Other Orthosis, spinal pedicle fixation, for degenerative disc disease devices
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- Vitality® 07.02011.001Biomet Spine LLC · Orthosis, spinal pedicle fixation, for degenerative disc disease3 recalls0 reports
- EXPEDIUM VERSE 199721001SMedos International Sàrl · Thoracolumbosacral pedicle screw system124 reports
- LineSider LS-N6SA7550Integrity Implants Inc. · Thoracolumbosacral Pedicle Screw System2 recalls1 report
- LineSider LS-N6SA6545Integrity Implants Inc. · Thoracolumbosacral Pedicle Screw System2 recalls0 reports
- EXPEDIUM VERSE 199721000SMedos International Sàrl · Thoracolumbosacral pedicle screw system97 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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