International safety notice
Corrective action for the Pressure Injectable Central Venous Catheter Product - Multiple-Lumen Central Venous Catheterization Product - Multiple-Lumen Central Venous Catheterization Product with ARROWg+ard® Antimicrobial Surface, Arrow International Inc.
Germany / BfArM · DEU · Jun 2, 2014
Key facts
| Title | Corrective action for the Pressure Injectable Central Venous Catheter Product - Multiple-Lumen Central Venous Catheterization Product - Multiple-Lumen Central Venous Catheterization Product with ARROWg+ard® Antimicrobial Surface, Arrow International Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Pressure Injectable Central Venous Catheter Product - Multiple-Lumen Central Venous Catheterization Product - Multiple-Lumen Central Venous Catheterization Product with ARROWg+ard® Antimicrobial Surface, Arrow International Inc. |
| Manufacturer | Corrective action for the Pressure Injectable Central Venous Catheter Product - Multiple-Lumen Central Venous Catheterization Product - Multiple-Lumen Central Venous Catheterization Product with ARROWg+ard® Antimicrobial Surface, Arrow International Inc. |
| Models | ASK-45854-PSLU, ASK-42854-SH, ASK-45854-UTMC, ASK-42854-PH, DE-24854-KGU, ASK-45854-PPP, GU-24854, ASK-45854-PUC, SE-15854-L, ASK-45854-PSFH, ASK-42854-FAH, ASK-45854-PUCI and 291 more |
| Date | Jun 2, 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