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Symmetry Rapidclean® 59-1200-BDRecalls & reported problems

Aspen Surgical Products, Inc. · RapidClean® Kerrison Rongeur, Micro, Thick Footplate, 40° Up, Ceramic Coated, Convertible, 1.0 mm, 8 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 00887482105467), received between Dec 16, 2015 and Dec 16, 2015.

The most frequently reported specific device problem is “Missing Value Reason” (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

  • Missing Value Reason1

Patient problems

  • No Code Available1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • Dec 16, 2015Missing Value Reason

    DURING SPINE SURGERY A KERRISION WAS USED TO EXTRACT BONE AND IT WAS NOTED THAT THE HANDLE WAS LOOSE AND THE SET SCREW WAS MISSING. MANUAL RETRIEVAL OF PART FROM THE WOUND WAS DONE. THE INSTRUMENT BROKE INTO TWO OR MORE PIECED DURING SURGERY, THERE WAS A DELAY IN TREATMENT. N O PATIENT HARM OR POTENTIAL HARM TO THE PATIENT AS A RESULT. INSTRUMENT WAS PART OF A TRIAL EVALUATION.

    Patient problems: No Code Available

    MAUDE report 5332379 ↗

Other Rongeur devices

All Rongeur devices →

Sources and updates

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