FDA Enforcement Class II Terminated

Central Venous Tray Triple Lumen Polyurethane Catheter, Catalog Identifier: C-UTLMY-501J-CCT Product Usage: The central venous catheter is designed for treatment of critically ill patients and is suggested for: 1. Continuous or intermittent drug infusions; 2. Central venous blood pressure monitoring (CVP); 3. Acute hyperalimentation; 4. Blood sampling; 5. Delivery of whole blood or blood products; 6. Simultaneous, separate infusion of drugs

Recall: Z-0633-2018 · Reported February 21, 2018

Enforcement

Recall Number
Z-0633-2018
Event ID
79050
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Cook Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
E-Mail
Report Date
February 21, 2018
Initiation Date
July 31, 2017
Classification Date
February 15, 2018
Termination Date
May 8, 2019
Address
750 N Daniels Way, Bloomington, IN, 47404-9120, United States

Description

Central Venous Tray Triple Lumen Polyurethane Catheter, Catalog Identifier: C-UTLMY-501J-CCT Product Usage: The central venous catheter is designed for treatment of critically ill patients and is suggested for: 1. Continuous or intermittent drug infusions; 2. Central venous blood pressure monitoring (CVP); 3. Acute hyperalimentation; 4. Blood sampling; 5. Delivery of whole blood or blood products; 6. Simultaneous, separate infusion of drugs

Reason

Central venous catheters may not fit over guide wire potentially causing procedure delay.

Code Info

Lot Number (Expiration date): 5901462 (30-January-2018)

Distribution

Worldwide distribution - US Nationwide in the states of: AL, CA, CO, FL, GA, IA, IL, KY, LA, MD, MI, MN, MO, NC, NY, OH, OK, OR, PA, RI, TN, TX, UT, VA, WA, WI; the District of Columbia and the countries of Belgium, India Italy, Spain, and United Kingdom.

Quantity

50