Symmetry RapidClean® 58-3200J-BDRecalls & reported problems
Aspen Surgical Products, Inc. · RapidClean® Kerrison Rongeur, Micro, Thin Footplate w/Ejector, 40° Up, 3 mm, Ceramic Coated, Convertible, 8 in, 203 mm · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00887482102527), received between Sep 18, 2015 and Nov 2, 2020 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Device Fell” (2 reports).
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
- Device Fell2
- Appropriate Device Problem Term/Code Not Available1
- Insufficient Device Problem Information1
- Material Separation1
- Missing Value Reason1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Missing Value Reason1
- No Consequences Or Impact To Patient1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 2, 2020Material Separation
THE SCREW CAME OUT OF THE KERRISON DURING THE PROCEDURE AND FELL INTO THE PATIENT. THE SCREW WAS RETRIEVED WITH NO HARM TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 10775096 ↗MalfunctionSep 9, 2020Device Fell
THE SCREW FELL OUT OF THE 3MM KERRISON AND FELL INTO THE SPINAL EREA. IT TOOK SOME TIME TO FIND THE SCREW, BUT IT WAS REMOVED WITH NO FURTHER HARM TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 10512221 ↗MalfunctionMar 24, 2020Device Fell
THE KERRISON FELL APART DURING A CASE. THE SCREW CAME OUT AND FELL INTO THE OPEN WOUND. THE SCREW WAS RETRIEVED AND THERE WAS NO HARM TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9875645 ↗Nov 10, 2015Missing Value Reason
SCREW KEPT COMING OUT, AND FELL INTO THE PATIENT. IT WAS RECOVERED. ITEM NEEDS TO BE EVALUATED AND REPLACED AS SOON AS POSSIBLE.
Patient problems: Missing Value Reason
MAUDE report 5246959 ↗Sep 18, 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 5107878 ↗
Other Rongeur devices
- SPOTLIGHT 292904201Depuy Spine, LLC · RONGEUR6 reports
- SPOTLIGHT 292904202Medos International Sàrl · 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
- SPOTLIGHT 292902240Depuy Spine, LLC · 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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