Device recall
Z-1924-2016: Tearaway Introducer, Model # VS203, VS303, 510 K # 130687, packaged individually…
FDA device recall · Class II · Medical Components, Inc dba MedComp
Key facts
| Recall number (Z-number) | Z-1924-2016 |
|---|---|
| Recall event | 74176 |
| Product | Tearaway Introducer, Model # VS203, VS303, 510 K # 130687, packaged individually in a pouch, 5 pouches per carton, lot # MBZ140, MBZL450, MBZV930 MBZZ490 Product Usage: The 2F and 3F Vascu-Sheath Tearaway Introducer is intended for percutaneous venous access by modified Seldinger Technique in… |
| Product code | DYB |
| Recalling firm | Medical Components, Inc dba MedComp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 16, 2017 |
| 510(k) numbers | K130687 |
| FEI number | 2518902 |
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