SYRINGES Adverse Event — Malfunction (MDR 1000113657-2020-00264)
SYRINGES Adverse Event — Malfunction (MDR 1000113657-2020-00264) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: SYRINGES; Generic name: PISTON SYRINGE; Manufacturer: TRIVIDIA HEALTH INC.
| Device | SYRINGES |
|---|---|
| Generic name | PISTON SYRINGE |
| Manufacturer | TRIVIDIA HEALTH INC |
| Report number | 1000113657-2020-00264 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | CONSUMER |
| Narrative | INTERNAL REPORT REFERENCE NUMBER: (B)(4). SYRINGES WERE NOT RETURNED FOR EVALUATION. MOST LIKELY UNDERLYING ROOT CAUSE: MLC-62: USER HAD POOR TECHNIQUE. NOTE: MANUFACTURER CONTACTED CUSTOMER IN A FOLLOW-UP CALL TO ENSURE THE REPLACEMENT PRODUCTS RESOLVED THE INITIAL CONCERN - ABLE TO ESTABLISH CONTACT WITH CUSTOMER AND STATED REPLACEMENT PRODUCT RESOLVED INITIAL CONCERN. |
| Source | openFDA MAUDE (device adverse events) |
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