RADIATION STERILIZED EXTENSION SETS Adverse Event — Injury (MDR 1416980-2020-02415)
RADIATION STERILIZED EXTENSION SETS Adverse Event — Injury (MDR 1416980-2020-02415) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: RADIATION STERILIZED EXTENSION SETS; Generic name: SET, ADMINISTRATION, INTRAVASCULAR; Manufacturer: BAXTER HEALTHCARE CORPORATION.
| Device | RADIATION STERILIZED EXTENSION SETS |
|---|---|
| Generic name | SET, ADMINISTRATION, INTRAVASCULAR |
| Manufacturer | BAXTER HEALTHCARE CORPORATION |
| Report number | 1416980-2020-02415 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | COMPANY REPRESENTATIVE, HEALTH |
| Narrative | ALTERNATE REPORTER PHONE NUMBER (CELL): (B)(6). DEVICE MANUFACTURER ADDRESS: (B)(4). SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. |
| Source | openFDA MAUDE (device adverse events) |
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