PNEUMOSTAT CHEST VALVE Adverse Event — Injury (MDR 3011175548-2020-00582)
PNEUMOSTAT CHEST VALVE Adverse Event — Injury (MDR 3011175548-2020-00582) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PNEUMOSTAT CHEST VALVE; Generic name: BOTTLE, COLLECTION, VACUUM; Manufacturer: ATRIUM MEDICAL CORPORATION.
| Device | PNEUMOSTAT CHEST VALVE |
|---|---|
| Generic name | BOTTLE, COLLECTION, VACUUM |
| Manufacturer | ATRIUM MEDICAL CORPORATION |
| Report number | 3011175548-2020-00582 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, FOREIG |
| Narrative | WE ARE UNABLE TO FULLY INVESTIGATE THIS REPORT AS NO PRODUCT NUMBER, LOT NUMBER OR SAMPLE WAS PROVIDED. IT IS NOT KNOWN WHAT RELATIONSHIP THE PNEUMOSTAT CHEST VALVE HAS TO THE REPORTED ADVERSE EVENTS. THE ARTICLE SUGGESTS THAT OUTPATIENT MANAGEMENT OF SELECTED PATIENTS WITH SSP MAY BE EFFECTIVE, SAFE AND COST-SAVING. BASED ON THE INFORMATION AVAILABLE ATRIUM HAS DETERMINED THAT THE EVENTS DESCRIBE |
| Source | openFDA MAUDE (device adverse events) |
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