Device recall
Z-0593-03: JOGRAPHY Cardiovascular Angiographic Catheter, 5F *** pigtail *** tapered with…
FDA device recall · Class II · Jomed Catheters, Inc.
Key facts
| Recall number (Z-number) | Z-0593-03 |
|---|---|
| Recall event | 25424 |
| Product | JOGRAPHY Cardiovascular Angiographic Catheter, 5F *** pigtail *** tapered with perfusion ports *** MEDI-DYNE, INC., 604 Queensbury Ave., Queensbury, New York 12804 *** Single use, sterile, disposable intravascular catheters with an atraumatic tip. |
| Recalling firm | Jomed Catheters, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 28, 2003 |
| 510(k) numbers | K000825 |
| FEI number | 1000120334 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
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