International safety notice
Corrective action for the Valved Entry Systems sold as stand-alone, within CONSTELLATION® TOTALPLUS® Paks, and within Alcon CUSTOM-PAKS, Alcon Laboratories Inc.
Germany / BfArM · DEU · Sep 21, 2015
Key facts
| Title | Corrective action for the Valved Entry Systems sold as stand-alone, within CONSTELLATION® TOTALPLUS® Paks, and within Alcon CUSTOM-PAKS, Alcon Laboratories Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Valved Entry Systems sold as stand-alone, within CONSTELLATION® TOTALPLUS® Paks, and within Alcon CUSTOM-PAKS, Alcon Laboratories Inc. |
| Manufacturer | Corrective action for the Valved Entry Systems sold as stand-alone, within CONSTELLATION® TOTALPLUS® Paks, and within Alcon CUSTOM-PAKS, Alcon Laboratories Inc. |
| Models | 8065751443, 99338, DE03680700300262658800, 1304-200, 79108, 1304-338, 1304-0, 8065750837, DE39313110, DEUTDE6FXXX, DE142102094 |
| Date | Sep 21, 2015 |
| 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