REFLECT 1244.1250SRecalls & reported problems
Globus Medical, Inc. · REFLECT 4.0mm Cord with Collet, 250mm · Class N
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00193982313449), received between Jun 11, 2025 and Jun 11, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Insufficient Device Problem Information1
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.
InjuryJun 11, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
IT WAS REPORTED THAT A REVISION SURGERY TOOK PLACE TO REMOVE THE END OF THE REFLECT TETHER THAT WAS LEFT IN THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22187341 ↗
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- The Tether™ 211H6032Zimmer Biomet Inc · Vertebral Body Tethering System6 reports
- The Tether™ 211H6030Zimmer Biomet Inc · Vertebral Body Tethering System4 reports
- The Tether™ 211H6035Zimmer Biomet Inc · Vertebral Body Tethering System3 reports
- The Tether™ 211H7040Zimmer Biomet Inc · Vertebral Body Tethering System2 reports
- The Tether™ 211H7035Zimmer Biomet Inc · Vertebral Body Tethering System2 reports
- The Tether™ 211H7037Zimmer Biomet Inc · Vertebral Body Tethering System2 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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