Device product
ARROWg+ard Blue MAC Two-Lumen Central Venous Access Kit The MAC(TM) Multi-Lumen Central Venous Access Device with ARROWg+ard Blue(R) permits venous access and catheter introduction to the central circulation. It may be inserted into the jugular, subclavian, or femoral veins. The ARROWg+ard(R) technology is intended to help provide protection against catheter-related infections. Clinical data have not been collected that demonstrate the use of the ARROWg+ard(R) antimicrobial surface in decreasing catheter-related infections for this device. It is not intended to be used as a treatment for existing infections, nor is it indicated for long-term use.
Z-2255-2017
Product summary
- Event
- Event 76937
- Status
- Terminated
- Classification
- Class II
- Quantity
- unknown-firm reports total devices distributed 43,394 eaches
- Official record key
device-enforcement:Z-2255-2017
Official wording
Reason: Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with certain Arrow products.
Code information: 510K # K011761 and Material numbers CDA-21242-1A, CDA-29803-1A, and CDA-29903-1A
Distribution pattern: Nationwide Distribution
Derived failure modes
-
Unknown
Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with certain Arrow products.