Mariner 41-6545-2Recalls & reported problems
Seaspine Orthopedics Corporation · Cannulated Screw 6.50 x 45mm · Class 2 · Implant
- 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 10889981068240), received between Mar 5, 2024 and Mar 5, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fracture” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Fracture1
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.
MalfunctionMar 5, 2024Fracture; Fracture
ON (B)(6) 2023, A PATIENT UNDERWENT SPINAL SURGERY CONSISTING OF THE MARINER MIS POSTERIOR FIXATION SYSTEM. SEASPINE WAS MADE AWARE ON 9 FEB 2024 THAT A 41-6545-2 CANNULATED SCREW 6.50 X 45MM HAD FRACTURED AT THE NECK AT S1. THE PATIENT IS ASYMPTOMATIC, AND NO REVISION SURGERY IS PLANNED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18839051 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.