Symmetry Rapidclean® 58-5230J-BDRecalls & reported problems
Aspen Surgical Products, Inc. · RapidClean® Rongeur, Micro, Thin Footplate w/Ejector, 40° Up, Creamic Coated, Convertible, 5 mm, 9 in · 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 00887482103203), received between Sep 15, 2015 and Sep 15, 2015.
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.
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available1
- Insufficient Device Problem Information1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
Sep 15, 2015Insufficient Device Problem Information; Appropriate Device Problem Term/Code Not Available
THE SCREW/PIN THAT SITS IN THE TOP PORTION OF THE KERRISON CAME APART FROM THE MAIN SHAFT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 5107980 ↗
Other Rongeur devices
- SPOTLIGHT 292904201Depuy Spine, LLC · RONGEUR6 reports
- 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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