Presource PBDS, Shoulder Arthroscopy, Kit, Circulator
Recall
- Recall Number
- Z-1200-2013
- Event Number
- 64736
- Firm
- Cardinal Health, Medical Products & Services 1430 Waukegan Road Attn V. Mueller Qa Park City IL 60085
- FEI Number
- 3001236905
- Product Code
- OFP
- Status
- Terminated
- Root Cause
- Packaging process control
- Initiated
- March 26, 2013
- Posted
- May 3, 2013
- Terminated
- April 12, 2017
Description
Presource PBDS, Shoulder Arthroscopy, Kit, Circulator
Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit that may contain outer plastic packaging on one or more components. If the packaging is removed without disassembling the components, remnants of the plastic from the packaging material may become lodged in the filter potentially causing an obstruction of airflow.
Affected consignees were notified with a letter, dated March 26, 2013, sent via FedEx Priority, of this action. Cardinal Sales Representatives will also be advised and will verbally communicate the action to affected customers. The letter identified the affected product and the problem. Customers are to locate any affected product and quarantine them. In addition, clinicians should be informed of the issue; and, warning labels should be affixed to the front of each kit instructing users to remove and discard the Anesthesia Circuit and Filter Assembly. In order to confirm receipt of this action and completion of labeling the product, the enclosed Acknowledgement Form should be completed and returned to the number provided. If customers do now wish to accept overlabeled product or to overlabel the product in their possession, they are to contact Presource Sales Operations at 800-766-0706, or their sales representative for further instruction. Customers are to contact Cardinal Health Quality Systems at 800-292-9332, if they have any questions or need special assistance.
Distributed in the states of AR, MS, SC, and TN.
4,571 Kits total