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AESCULAP FF843RRecalls & reported problems

Aesculap AG · CASPAR Rongeur, 150 °, upwards cutting, 6" (155 mm), width: 3 mm · Class 1

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04038653044719), received between Jun 2, 2021 and Jun 2, 2021 — classified as 1 injury.

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Break1
  • Fracture1

Patient problems

  • Foreign Body In Patient1
  • Insufficient Information1

Recent adverse event reports

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

  • InjuryJun 2, 2021Break; Fracture; Break; Fracture

    IT WAS REPORTED THAT THERE WAS AN ISSUE WITH FF843R - CASPAR RONGEUR UP-BITE 3MM155MM. ACCORDING TO THE COMPLAINT DESCRIPTION, A RONGEUR WITH REFERENCE FF843R IS BROKEN DURING A SPINE SURGERY ON (B)(6) 2017. A PIECE OF THE RONGEUR REMAINED IN THE BODY OF THE PATIENT. A REVISION SURGERY WAS NECESSARY. ADDITIONAL INFORMATION RECEIVED CONFIRMED THAT THE SPECIFIC PIECE OF THE RONGEUR HAS BEEN REMOVED (D.D. END (B)(6)/BEGINNING OF (B)(6)). THE ADVERSE EVENT IS FILED UNDER (B)(4).

    Patient problems: Foreign Body In Patient; Insufficient Information

    MAUDE report 11923458 ↗

Other RONGEUR devices

All RONGEUR devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.