Explorer TO ET1-302808Recalls & reported problems
Seaspine Orthopedics Corporation · Height Expansion, 9mm x 28mm x 8-12mm, 0 Deg · Class 2 · Implant
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 10889981206505), received between Jan 23, 2023 and Jan 23, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Collapse” (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
- Collapse1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 23, 2023Collapse; Collapse
ON (B)(6) 2022 A PATIENT UNDERWENT SPINAL SURGERY CONSISTING OF SEASPINE'S EXPLORER TO SYSTEM. AT THE FOUR-MONTH POST-OP VISIT, IT WAS IDENTIFIED THAT THE EXPANDABLE IMPLANT HAD COLLAPSED. SEASPINE WAS MADE AWARE OF THIS EVENT ON (B)(6) 2022. THERE ARE NO PLANS FOR REVISION OR REMOVAL CURRENTLY. NO FURTHER INFORMATION HAS BEEN PROVIDED ABOUT THE PATIENT'S CONDITION.
Patient problems: Insufficient Information
MAUDE report 16230462 ↗
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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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