SILVER Adverse Event — Malfunction (MDR 2648035-2020-00393)
SILVER Adverse Event — Malfunction (MDR 2648035-2020-00393) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: SILVER; Generic name: SURGICAL ADJUNCTS; Manufacturer: JOHNSON & JOHNSON SURGICAL VISION, INC..
| Device | SILVER |
|---|---|
| Generic name | SURGICAL ADJUNCTS |
| Manufacturer | JOHNSON & JOHNSON SURGICAL VISION, INC. |
| Report number | 2648035-2020-00393 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Narrative | ADDITIONAL INFORMATION: BREAKDOWN OF 9 EVENTS ARE AS FOLLOWS: CARTRIDGE CRACK, LENS DAMAGED: 1, CARTRIDGE TIP CRACKED/DAMAGED, DELIVERY ISSUE, DIFFICULT TO USE, LOADING ISSUES: 5, CARTRIDGE TIP CRACKED/DAMAGED, DELIVERY ISSUE, STUCK IN CARTRIDGE: 1, CARTRIDGE TIP CRACKED/DAMAGED, HAPTIC DAMAGED, OVERRIDE: 1, DIFFICULT TO USE, HAPTIC DETACHED: 1. LOT NUMBERS OF SUSPECT PRODUCTS: UNKNOWN - 1, CE0975 |
| Source | openFDA MAUDE (device adverse events) |
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