12MM/125 DEG TI CANN TFNA 400MM/RIGHT ¿ STERILE Adverse Event — Injury (MDR 8030965-2020-03116)
12MM/125 DEG TI CANN TFNA 400MM/RIGHT ¿ STERILE Adverse Event — Injury (MDR 8030965-2020-03116) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: 12MM/125 DEG TI CANN TFNA 400MM/RIGHT ¿ STERILE; Generic name: ROD,FIXATION,INTRAMEDULLARY; Manufacturer: OBERDORF SYNTHES PRODUKTIONS
| Device | 12MM/125 DEG TI CANN TFNA 400MM/RIGHT ¿ STERILE |
|---|---|
| Generic name | ROD,FIXATION,INTRAMEDULLARY |
| Manufacturer | OBERDORF SYNTHES PRODUKTIONS GMBH |
| Report number | 8030965-2020-03116 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, FOREIG |
| Narrative | DATE OF EVENT: ONLY EVENT YEAR IS KNOWN: 2020. COMPLAINANT PART IS NOT EXPECTED TO BE RETURNED FOR MANUFACTURER REVIEW/INVESTIGATION. MANUFACTURING LOCATION: (B)(4). MANUFACTURING DATE: MAY 21, 2019. EXPIRATION DATE: MAY 1, 2029. PART NUMBER: 04.037.231S, 12MM/125 DEG TI CANN TFNA 400MM/RIGHT- STERILE. LOT NUMBER: 3L24126 (STERILE). LOT QUANTITY: (B)(4). PRODUCTION ORDER TRAVELER MET ALL INSPECTIO |
| Source | openFDA MAUDE (device adverse events) |
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