FDA Enforcement Class II Terminated

T090-000 90" 20 Drop IV Admin Set. 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-2223-2016 · Reported July 27, 2016

Enforcement

Recall Number
Z-2223-2016
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

T090-000 90" 20 Drop IV Admin Set. 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: 020-300197. Lot Number: 1406082, 1407122, 1408126, 1408128, 1410078D, 1410079D, 1410080D, 1410081D, 1410082D, 1411025D, 1411026D, 1501022D, 1501109D, 1503083D, 1507012D

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

2757 cases