Device recall
Z-2074-2012: BridgePoint Medical, Stingray Catheter, REF M - 1000, Sterilized with Ethylene…
FDA device recall · Class II · Bridgepoint Medical
Key facts
| Recall number (Z-number) | Z-2074-2012 |
|---|---|
| Recall event | 62450 |
| Product | BridgePoint Medical, Stingray Catheter, REF M - 1000, Sterilized with Ethylene Oxide Gas, Prescription Only, Manufacturer BridgePoint Medical Inc. 13355 10th Ave N, Suite 110, Plymouth, MN 55441. Stingray" Catheters are intended to facilitate the intraluminal placement of conventional guidewires… |
| Product code | DQY |
| Recalling firm | Bridgepoint Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 6, 2012 |
| 510(k) numbers | K080987, K101591, K102725 |
| FEI number | 3002095335 |
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