BD POSIFLUSH XS PRE-FILLED FLUSH SYRINGE NACL 0.9% Adverse Event — Malfunction (MDR 9616657-2020-00065)
BD POSIFLUSH XS PRE-FILLED FLUSH SYRINGE NACL 0.9% Adverse Event — Malfunction (MDR 9616657-2020-00065) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: BD POSIFLUSH XS PRE-FILLED FLUSH SYRINGE NACL 0.9%; Generic name: SALINE VASCULAR ACCESS FLUSH; Manufacturer: BECTON, DICKINSON
| Device | BD POSIFLUSH XS PRE-FILLED FLUSH SYRINGE NACL 0.9% |
|---|---|
| Generic name | SALINE VASCULAR ACCESS FLUSH |
| Manufacturer | BECTON, DICKINSON AND CO. |
| Report number | 9616657-2020-00065 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | DISTRIBUTOR, FOREIGN, OTHER |
| Narrative | THERE WERE MULTIPLE LOT NUMBERS REPORTED TO BE INVOLVED. THE INFORMATION FOR EACH LOT NUMBER IS AS FOLLOWS: MEDICAL DEVICE LOT #: 9101610, MEDICAL DEVICE EXPIRATION DATE: 2022-03-31, DEVICE MANUFACTURE DATE: 2019-04-11, MEDICAL DEVICE LOT #: 9004801, MEDICAL DEVICE EXPIRATION DATE: 2021-12-31, DEVICE MANUFACTURE DATE: 2019-01-04, MEDICAL DEVICE LOT #: 9074905, MEDICAL DEVICE EXPIRATION DATE: 2022- |
| Source | openFDA MAUDE (device adverse events) |
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