International safety notice
Lot Recall for Z-Med II Percutaneous Transluminal Valvuloplasty Catheters and COEfficient Pediatric Valvuloplasty Catheters, NuMED Canada Inc.
Germany / BfArM · DEU · Apr 12, 2011
Key facts
| Title | Lot Recall for Z-Med II Percutaneous Transluminal Valvuloplasty Catheters and COEfficient Pediatric Valvuloplasty Catheters, NuMED Canada Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Z-Med II Percutaneous Transluminal Valvuloplasty Catheters and COEfficient Pediatric Valvuloplasty Catheters, NuMED Canada Inc. |
| Manufacturer | Lot Recall for Z-Med II Percutaneous Transluminal Valvuloplasty Catheters and COEfficient Pediatric Valvuloplasty Catheters, NuMED Canada Inc. |
| Models | 4X6X6X, JZ-7675, 0.021, PDC404, PDC527, Y-2030, JZ-7536, COE125, PTS303, TH-14770, TH-14717, PTS403 and 81 more |
| Date | Apr 12, 2011 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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