Malibu™ 12-1040Recalls & reported problems
Seaspine Orthopedics Corporation · PRECONTOURED ROD, 5.5 x 40mm · Class 2 · Implant
All models of Malibu (17)
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 10889981029951), received between Aug 2, 2016 and Aug 2, 2016 — 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Fracture1
- Mechanical Problem1
Patient problems
- Failure of Implant1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 2, 2016Fracture; Mechanical Problem; Fracture; Mechanical Problem
WITH INITIAL SURGERY COMPLETED ON (B)(6) 2015, REVIEW OF THE EVENT RADIOGRAPHS AT 17 MONTHS DEPICTS LIMITED FUSION BETWEEN L4-L5 VERTEBRAL BODIES. PATIENT STATUS IS UNKNOWN. REVISION SURGERY IS PLANNED, SCHEDULE DATE UNKNOWN.
Patient problems: Failure of Implant
MAUDE report 5842118 ↗
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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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