Symmetry DECKER 53-4002Recalls & reported problems
Aspen Surgical Products, Inc. · Symmetry® Rongeur; Decker Micro; Curved Left; 152 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 00887482023457), received between Jun 23, 2022 and Jun 23, 2022 — 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.
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.
MalfunctionJun 23, 2022Break
THE CUSTOMER ALLEGED THAT WHILE USING THE MICRO PITUITARY RONGEUR, THE INSTRUMENT BROKE AT THE TIP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14794634 ↗
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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