Recall Z-0109-2014— Baxter Healthcare Corp.
Class II · Terminated
Class II FDA medical device recall by Baxter Healthcare Corp., initiated 2013-08-30, terminated 2017-04-19. FDA's recall record names no specific 510(k) clearance for this event. Product: Vented Spike Adapter Product Code 2C0471, Sterile, nopyrogenic. Manufactured by an affiliate of Baxter Healthcare Corporation, Clintec Nutrition Division, Deerfield IL 60015 USA. An IV transfer device, used to transfer fluids in pharmacy compounding system.. Reason: Potential tears in the pouch of six lots of Vented Spike Adapter Product Code 2C0471.
- Recalling firm
- Baxter Healthcare Corp.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2013-08-30
- Terminated
- 2017-04-19
- Firm location
- Deerfield, IL, United States
Product description
Vented Spike Adapter Product Code 2C0471, Sterile, nopyrogenic. Manufactured by an affiliate of Baxter Healthcare Corporation, Clintec Nutrition Division, Deerfield IL 60015 USA. An IV transfer device, used to transfer fluids in pharmacy compounding system.
Reason for recall
Potential tears in the pouch of six lots of Vented Spike Adapter Product Code 2C0471
Data sourced from openFDA. This site is unofficial and independent of the FDA.