Devices

Device Recall Baxter Solution Set with DuoVent Spike

Model / Serial
Product Code 1C8507s, lot numbers GR291542, GR292409, GR292797 and GR294454.
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
(USA) Nationwide Distribution including the states of Alabama, California, Iowa, Illinois, Indiana, Massachusetts, Maryland, Michigan, North Carolina, New Hampshire, Ohio, Pennsylvania, Tennessee and Virginia.
Product Description
Baxter Solution Set with Duo-Vent Spike; 109" (2.8 m), Male Luer Lock Adapter 10 drops/mL. || Baxter Healthcare Corporation. || A sterile, single use, nonpyrogenic fluid pathway for use with rigid nonvented and flexible containers.
Manufacturer
Baxter Healthcare Corp.
1 Event
- Recall of Device Recall Baxter Solution Set with DuoVent Spike

Manufacturer

Baxter Healthcare Corp.

Manufacturer Address
Baxter Healthcare Corp., Rt. 120 & Wilson Rd, Round Lake IL 60073
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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