Device recall
Z-2069-2021: Arrow Temporary Pacing Catheter/Introducer Kit 6Fr. pacing catheter 7Fr…
FDA device recall · Class II · Arrow International Inc
Key facts
| Recall number (Z-number) | Z-2069-2021 |
|---|---|
| Recall event | 88120 |
| Product | Arrow Temporary Pacing Catheter/Introducer Kit 6Fr. pacing catheter 7Fr. introducer Product Code: AI-06210-IK - Product Usage: intended for temporary use in electrophysiology studies for intracardiac stimulation and/or ECG recording. |
| Recalling firm | Arrow International Inc |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3015859709 |
At a glance
- None 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