MAUDE report
MAUDE report 9545: MISTY OX (OXYGEN PREFILLED DISPOSABLE NEBULIZER) 500ML NACL.
No Answer Provided · received Jun 9, 1993 · AMERICAN MOLDING CORPORATION
Key facts
| MDR report key | 9545 |
|---|---|
| Report number | 9545 |
| Event type | No Answer Provided |
| Brand name | MISTY OX (OXYGEN PREFILLED DISPOSABLE NEBULIZER) 500ML NACL. |
| Manufacturer | AMERICAN MOLDING CORPORATION |
| Date received by FDA | Jun 9, 1993 |
| Report date | Jun 3, 1993 |
| Report source | Maude |
At a glance
- None Device problems coded
- 1–9 MAUDE reports for this brand
- None Death reports for this brand
- None Injury reports for this brand
- Yes Product problem flagged
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About MAUDE medical device reports
MAUDE holds medical device reports (MDRs) of suspected device-associated deaths, serious injuries and malfunctions submitted to the FDA by manufacturers, importers, user facilities and the public. A report alone does not establish that a device caused an event.
Source: U.S. Food and Drug Administration (FDA), MAUDE (Manufacturer and User Facility Device Experience) database · Source date: