MAUDE manufacturer profile
ABBOTT · MMX
MAUDE profile for Device, Percutaneous Retrieval
Key facts
| Manufacturer | ABBOTT |
|---|---|
| Manufacturer group | ABBOTT |
| Product code | MMX |
| Product code name | Device, Percutaneous Retrieval |
At a glance
- 1–9 MAUDE reports
- 1–9 Death reports
- 1–9 Injury reports
- 1–9 Malfunction reports
- 1–9 Problems flagged by Orca1 signal analytics
- Connection Problem, No Clinical Signs, Symptoms or Conditions, Appropriate Term / Code Not Available, Adverse Event Without Identified Device or Use Problem, Obstruction of Flow, Cardiac Tamponade, Cardiac Perforation, Pericardial Effusion 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