Device recall
Z-0434-2011: LeMaitre VascuTape Radiopaque Tape, LeMaitre Stent Guide, 100 strips Catalog…
FDA device recall · Class III · Lemaitre Vascular, Inc.
Key facts
| Recall number (Z-number) | Z-0434-2011 |
|---|---|
| Recall event | 57028 |
| Product | LeMaitre VascuTape Radiopaque Tape, LeMaitre Stent Guide, 100 strips Catalog Number: 1102-00 Intended to be placed on the patient's skin to assist during imaging procedures by serving as an internal frame of reference. |
| Product code | FTY |
| Recalling firm | Lemaitre Vascular, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 15, 2011 |
| 510(k) numbers | K932184 |
| FEI number | 1220948 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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