Device recall
Z-2288-2020: Arrow FlexTip Plus Epidural Kit with NRFit Connector, catheter system, Product…
FDA device recall · Class II · Arrow International Inc
Key facts
| Recall number (Z-number) | Z-2288-2020 |
|---|---|
| Recall event | 85645 |
| Product | Arrow FlexTip Plus Epidural Kit with NRFit Connector, catheter system, Product Codes (US) OT19TAGSK OT19TAGSKA OT19TAPSK OT19TCGLK Product Codes (OUS) AT-05501-NRF OT19HBPSS UM-05400-NRF ASK-05500-NRON EJ-05400-NRON OU-05500-NRON TU-05500-NRON The Arrow Epidural Catheter kit permits access to the… |
| Product code | BSO |
| Recalling firm | Arrow International Inc |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K140110 |
| FEI number | 3015859709 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database