Devices

Device Recall Baxter Solution Set for Epidural Use

Model / Serial
product code 2C7554s, lot GR293209 *** The recall was expanded to include lots GR291559 and GR294928 ***
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution - USA including Alabama, Arizona, California, Illinois, Kentucky, Louisiana, New Mexico, North Carolina, Ohio, Oregon, Tennessee and Washington, and internationally to Canada and South Africa.
Product Description
Baxter Solution Set for Epidural Use, 110" (2.8 m), Male Luer Lock Adapter; a sterile, single use, nonpyrogenic fluid pathway for use with 6200 and 6300 series Flo-Gard Volumetric Infusion Pumps; Baxter Healthcare corporation, Deerfield, IL; product code 2C7554s || The tubing set is intended for use with Flo-Gard Infusion Pumps to provide epidural delivery of anesthetic or analgesic drugs for periods up to 96 hours.
Manufacturer
Baxter Healthcare Corp.
1 Event
- Recall of Device Recall Baxter Solution Set for Epidural Use

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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