FDA Enforcement Class II Terminated

T100-000WF, IV Set with Upper Y-Site, Lower Y-Site, Back Check Valve, and Free Flow Clip. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.

Recall: Z-2231-2016 · Reported July 27, 2016

Enforcement

Recall Number
Z-2231-2016
Event ID
74437
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
WalkMed Infusion, LLC
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
N/A
Report Date
July 27, 2016
Initiation Date
June 14, 2016
Classification Date
July 18, 2016
Termination Date
December 1, 2016
Address
6555 S Kenton St Ste 304, N/A, Englewood, CO, 80111-6838, United States

Description

T100-000WF, IV Set with Upper Y-Site, Lower Y-Site, Back Check Valve, and Free Flow Clip. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.

Reason

WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton Administration Sets Due to the Potential Presence of Particulate In or On the Administration Sets.

Code Info

Product Number: 020-300644. Lot Number: 1406019, 1406020, 1407020, 1407021, 1407022, 1407120, 1407121, 1408133, 1501111D, 1506067D, 1507020D, 1507060D, 1508073D

Distribution

US Nationwide Distribution in the states of AL, AZ, CA, FL, IL, MA, MS, NJ, NV, NY, OH, PA, TN, UT, and WA.

Quantity

2198 cases