International safety notice
Corrective Action for Dimension Vista V-LYTE fluids, Siemens Healthcare
Germany / BfArM · DEU · Jan 19, 2012
Key facts
| Title | Corrective Action for Dimension Vista V-LYTE fluids, Siemens Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Dimension Vista V-LYTE fluids, Siemens Healthcare |
| Manufacturer | Corrective Action for Dimension Vista V-LYTE fluids, Siemens Healthcare |
| Models | KA1G01, KA1J01, 19714-6101, 11-16, 888-588-3916, KE1J01, KB1K01, KB1J01, KE1H01, KA1H01, 302-631-8467, 800-441-9250 and 3 more |
| Date | Jan 19, 2012 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 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