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AESCULAP BB524Recalls & reported problems

Aesculap AG · Scalpel Blades, Fig. 24, carbon steel, sterile, disposable, dispenser packaging, package of 100 pieces · Class 1

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 04038653020027), received between Oct 12, 2021 and Oct 12, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Delivered as Unsterile Product” (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

  • Delivered as Unsterile Product1
  • Nonstandard Device1

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.

  • MalfunctionOct 12, 2021Nonstandard Device; Delivered as Unsterile Product; Nonstandard Device; Delivered as Unsterile Product

    IT WAS REPORTED THAT THERE WAS AN ISSUE WITH BB524 - CARBON STEEL SCALPEL BLADES #24. ACCORDING TO THE COMPLAINT DESCRIPTION, THE CARBON STEEL SCALPEL BLADES ARE NON STERILE. THERE WAS NO DESCRIBED PATIENT HARM. ADDITIONAL INFORMATION WAS NOT PROVIDED. ADDITIONAL PATIENT INFORMATION IS NOT AVAILABLE. THE MALFUNCTION IS FILED UNDER (B)(4).

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12618020 ↗

Other BLADE, SCALPEL devices

All BLADE, SCALPEL devices →

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