LOCKING TITANIUM ADAPTER Adverse Event — Malfunction (MDR 1416980-2020-02398)
LOCKING TITANIUM ADAPTER Adverse Event — Malfunction (MDR 1416980-2020-02398) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: LOCKING TITANIUM ADAPTER; Generic name: SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE; Manufacturer: BAXTER HEALTHCARE CORPORATION.
| Device | LOCKING TITANIUM ADAPTER |
|---|---|
| Generic name | SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE |
| Manufacturer | BAXTER HEALTHCARE CORPORATION |
| Report number | 1416980-2020-02398 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, FOREIG |
| Narrative | ADDITIONAL INFORMATION: D10, H3, AND H6. THE ACTUAL DEVICE WAS RETURNED FOR EVALUATION. VISUAL INSPECTION DID NOT IDENTIFY ANY ABNORMALITIES THAT COULD HAVE CONTRIBUTED TO THE REPORTED CONDITION. A CONNECTION TEST AND DIMENSIONAL INSPECTION WERE PERFORMED WITH NO ISSUES; ALL SPECIFICATIONS WERE MET. THE DEVICE WAS FOUND TO BE CONFORMING PRODUCT. THE REPORTED CONDITION WAS NOT VERIFIED. SHOULD ADDI |
| Source | openFDA MAUDE (device adverse events) |
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