MAUDE manufacturer profile

CODMAN AND SHURTLEFF, INC · HCG

MAUDE profile for Device, Neurovascular Embolization

Key facts

Manufacturer CODMAN AND SHURTLEFF, INC
Manufacturer group CODMAN AND SHURTLEFF, INC
Product code HCG
Product code name Device, Neurovascular Embolization

At a glance

  • 100–999 MAUDE reports
  • 10–99 Death reports
  • 100–999 Injury reports
  • 100–999 Malfunction reports
  • 10–99 Problems flagged by Orca1 signal analytics
  • No Consequences Or Impact To Patient, Stretched, Positioning Failure, Physical Resistance, Premature Activation, Adverse Event Without Identified Device or Use Problem, Difficult To Position, Failure to Advance Most reported problems

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About MAUDE manufacturer and product code profiles

Manufacturer profiles aggregate MAUDE reports for one manufacturer within one product code, the level at which device safety signals are usually reviewed.

Source: U.S. Food and Drug Administration (FDA), MAUDE database; aggregation by Orca1

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