International safety notice
Recall for the Coherex WaveCrest® Left Atrial Appendage (LAA) Occlusion System and Delivery Sheath, Coherex Medical Inc.
Germany / BfArM · DEU · Aug 18, 2014
Key facts
| Title | Recall for the Coherex WaveCrest® Left Atrial Appendage (LAA) Occlusion System and Delivery Sheath, Coherex Medical Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Coherex WaveCrest® Left Atrial Appendage (LAA) Occlusion System and Delivery Sheath, Coherex Medical Inc. |
| Manufacturer | Recall for the Coherex WaveCrest® Left Atrial Appendage (LAA) Occlusion System and Delivery Sheath, Coherex Medical Inc. |
| Models | 801-433-9900, 4547005, WCR1523, 22851, 84104, WCR1513, WCR1541, 800-390-9107, WCR1540, 390-9107, 49-172-4547005, WCR1503 and 3 more |
| Date | Aug 18, 2014 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1