FDA Recall Terminated

Lifeguard Infusion Set with Smartsite, 20Ga, 1, CLGY-2010 Huber type needle set used for the infusion of medical fluids into implantable ports.

Recall: Z-0914-2013 · Initiated January 21, 2013

Recall

Recall Number
Z-0914-2013
Event Number
64464
Firm
Churchill Medical Systems, Inc.
FEI Number
1000120555
Product Code
FPA
Status
Terminated
Root Cause
Under Investigation by firm
Initiated
January 21, 2013
Posted
March 6, 2013
Terminated
September 10, 2013
Address
87 Venture Drive, Dover, NH, 03820-5914

Description

Lifeguard Infusion Set with Smartsite, 20Ga, 1, CLGY-2010 Huber type needle set used for the infusion of medical fluids into implantable ports.

Reason

The label on the device states that the item number is CLGY-2210 when the item number on the device label should read CLGY-2010. This is a 20Ga Huber needle set; however, the product label states the pouch contains a 22Ga set.

Action

Vycon sent an Urgent Medical Device Recall letter dated January 21, 2013, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed check their stock for the affected product and immediately cease use and distribution and quarantine all affected product immediately. Count and document their affected inventory on the Recall Acknowledgement and Inventory Return Form. Customers were instructed to fax or email the form to Vygon including customer contact information. All affected product would be credited or replaced at no cost to the customer. Customers with questions were instructed to call 1-800-473-5414, or by e-mail at [email protected]. For questions regarding this recall call 603-743-5988.

Distribution

Nationwide Distribution including MO, IL, FL, PA, VA, MO, NY, NE, NH, and OH.

Quantity

2340