Integra® Ruggles®-Redmond™ RN5980Recalls & reported problems
Integra Lifesciences Production Corporation · Integra® Ruggles®-Redmond™ Cushing Ivd Rongeur, 9", Straight, 1.5x10mm Bite · Class 1
Data updated Oct 18, 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 10381780372868), received between Dec 12, 2025 and Dec 12, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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
- Break1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 12, 2025Break; Break
THE FOLLOWING WAS REPORTED VIA MEDWATCH/MDR REPORT #MW5178401: A MEDWATCH/MDR REPORT (#MW5178401) INDICATED THAT, DURING A SPINE SURGERY, THE TIP OF A RUGGLES CUSHING IVD STRAIGHT 9 INCHES 1.5M (RN5980) BROKE OFF WITHIN THE DISC SPACE. THE DETACHED TIP WAS SUCCESSFULLY RETRIEVED USING A MAGNET, AND THE SURGICAL TEAM VERIFIED THAT NO FOREIGN BODY REMAINED. THE INCIDENT RESULTED IN A SURGICAL DELAY, THOUGH THE DURATION WAS NOT SPECIFIED. NO PATIENT INJURY WAS REPORTED
Patient problems: Foreign Body In Patient
MAUDE report 23789226 ↗
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- SPOTLIGHT 292904202Medos International Sàrl · RONGEUR5 reports
- Symmetry RapidClean® 58-3200J-BDAspen Surgical Products, Inc. · Rongeur5 reports
- NA 03.605.001Synthes GmbH · RONGEUR4 reports
- Medicon 57.28.33Medicon eG. Chirurgiemechaniker-Genossenschaft · RONGEUR3 reports
- Symmetry Rapidclean® 58-3200-BDAspen Surgical Products, Inc. · Rongeur3 reports
- AESCULAP FF805RAesculap AG · RONGEUR3 reports
- Integra® Jarit® 280405Integra Lifesciences Production Corporation · RONGEUR3 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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