Symmetry Rapidclean® 53-1612LDRecalls & reported problems
Aspen Surgical Products, Inc. · RapidClean Kerrison Rongeur; Detachable Lumbar w/Ejector; 40° Up; 2 mm; 7 in; 178 mm · Class 2
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 00887482034491), received between Feb 17, 2026 and Feb 17, 2026 — 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
- 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.
MalfunctionFeb 17, 2026Break
COMPLAINANT ALLEGES "THE TIP COMPONENT CONSISTENTLY BREAKS AT THE SAME POINT, WHICH HAS CAUSED REPEATED FAILURES IN CLINICAL USE."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24365894 ↗
Other Rongeur, Manual devices
- Symmetry DECKER 53-4000Aspen Surgical Products, Inc. · Rongeur, Manual3 reports
- Integra® Miltex® 26-332Integra Lifesciences Production Corporation · RONGEUR, MANUAL3 reports
- V. Mueller NL4291-81TSteris Corporation · RONGEUR, MANUAL2 reports
- Symmetry Rapidclean® 53-1624LDAspen Surgical Products, Inc. · Rongeur, Manual2 reports
- V. Mueller NL6147Steris Corporation · RONGEUR, MANUAL2 reports
- Symmetry FERRIS-SMITH 53-1160Aspen Surgical Products, Inc. · Rongeur, Manual2 reports
- Symmetry FERRIS-SMITH 53-1165Aspen Surgical Products, Inc. · Rongeur, Manual1 report
- NA TEB-2XFehling Instruments GmbH & Co. KG · Rongeur, Manual1 report
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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