PROTECTOR P53 Adverse Event — Malfunction (MDR 3003152976-2020-00182)
PROTECTOR P53 Adverse Event — Malfunction (MDR 3003152976-2020-00182) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PROTECTOR P53; Generic name: INTRAVASCULAR ADMINISTRATION SET; Manufacturer: BECTON DICKINSON, S.A..
| Device | PROTECTOR P53 |
|---|---|
| Generic name | INTRAVASCULAR ADMINISTRATION SET |
| Manufacturer | BECTON DICKINSON, S.A. |
| Report number | 3003152976-2020-00182 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | FOREIGN, OTHER, USER FACILITY |
| Narrative | THERE WERE MULTIPLE LOT NUMBERS REPORTED TO BE INVOLVED. THE INFORMATION FOR EACH LOT NUMBER IS AS FOLLOWS: MEDICAL DEVICE LOT #: 1611518, MEDICAL DEVICE EXPIRATION DATE: 2021-11-22, DEVICE MANUFACTURE DATE: 2016-11-30. MEDICAL DEVICE LOT #: 1910112, MEDICAL DEVICE EXPIRATION DATE: 2024-09-30, DEVICE MANUFACTURE DATE: 2019-10-15. A DEVICE EVALUATION IS ANTICIPATED, BUT HAS NOT YET BEGUN. UPON COMP |
| Source | openFDA MAUDE (device adverse events) |
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