SVCE REPL SPIDER 2 TENET 7615 Adverse Event — Malfunction (MDR 1643264-2020-00220)
SVCE REPL SPIDER 2 TENET 7615 Adverse Event — Malfunction (MDR 1643264-2020-00220) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: SVCE REPL SPIDER 2 TENET 7615; Generic name: TABLE, OPERATING-ROOM, ELECTRICAL; Manufacturer: SMITH & NEPHEW, INC..
| Device | SVCE REPL SPIDER 2 TENET 7615 |
|---|---|
| Generic name | TABLE, OPERATING-ROOM, ELECTRICAL |
| Manufacturer | SMITH & NEPHEW, INC. |
| Report number | 1643264-2020-00220 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, HEALTH |
| Narrative | IT WAS REPORTED THAT DURING AN UNKNOWN SURGERY, THE SPIDER 2 TENET DID NOT AUTO LOCK. THERE WAS A LOSS OF TRACTION. THE PROCEDURE WAS COMPLETED WITHOUT DELAY USING A BACK-UP DEVICE. NO PATIENT INJURY OR OTHER COMPLICATIONS WERE REPORTED. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED. IF ADDITIONAL INFORMATION SHOULD BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED ACCORDINGLY. |
| Source | openFDA MAUDE (device adverse events) |
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