PLATINUM 1 SERIES Adverse Event — Malfunction (MDR 2648035-2020-00398)
PLATINUM 1 SERIES Adverse Event — Malfunction (MDR 2648035-2020-00398) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PLATINUM 1 SERIES; Generic name: SURGICAL ADJUNCTS; Manufacturer: JOHNSON & JOHNSON SURGICAL VISION, INC..
| Device | PLATINUM 1 SERIES |
|---|---|
| Generic name | SURGICAL ADJUNCTS |
| Manufacturer | JOHNSON & JOHNSON SURGICAL VISION, INC. |
| Report number | 2648035-2020-00398 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | HEALTH PROFESSIONAL, USER FACI |
| Narrative | ADDITIONAL INFORMATION: AGE/DATE OF BIRTH: UNKNOWN, INFORMATION NOT PROVIDED. EXPIRATION DATE: UNKNOWN, AS LOT NUMBER WAS NOT PROVIDED. UNIQUE IDENTIFIER: A COMPLETE UDI# IS UNKNOWN AS THE LOT# WAS NOT PROVIDED. IF IMPLANTED, GIVE DATE: NOT APPLICABLE AS THE CARTRIDGE IS NOT AN IMPLANTABLE DEVICE. IF EXPLANTED, GIVE DATE: NOT APPLICABLE AS THE CARTRIDGE IS NOT AN IMPLANTABLE DEVICE. DEVICE MANUFAC |
| Source | openFDA MAUDE (device adverse events) |
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