• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Enforcement Report - Week of June 12, 2013

  • Print
  • Share
  • E-mail
-

Product Detail

Product Description I-Flow ON-Q Pain Relief System, T-Block Needle/Catheter Kit, Model #TB089T The intended use of each component in the finished final trays is consistent with the intended use of the component stated in the respective 510(k) submission.
Recall Number Z-1445-2013
Classification Class II
Code Info Lot # AW207202U
Product Distributed Qty 75 units
Reason For Recall I-Flow initiated two voluntary product removals of the ON-Q Pain Relief System: T-Block Needle/Catheter Tray and T-Block Needle/Catheter Kit because they may have potentially malfunctioned.

Event Detail

Event Id 64826
Product Type Devices
Status Completed
Recalling Firm I-Flow LLC
City Lake Forest
State CA
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2012-06-01
Initial Firm Notification of Consignee or Public E-Mail
Distribution Pattern Nationwide distribution: USA including states of: CA, CT, FL, IL, IN, KY, NY, OH, OR, TN, TX, VA and WI.
-
-