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U.S. Department of Health and Human Services

Enforcement Report - Week of December 11, 2013

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Product Detail

Product Description VersaSafe Extension Set, Model No. 21000M-007
Recall Number Z-0435-2014
Classification Class II
Code Info Lot No. 13066550
Product Distributed Qty 3500 units
Reason For Recall CareFusion is recalling the VersaSafe Extension Intravascular Administration Set because it may have excessive adhesive which will prevent the male spin collar to operate as intended.

Event Detail

Event Id 66758
Product Type Devices
Status Ongoing
Recalling Firm CareFusion 303, Inc.
City San Diego
State CA
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2013-11-08
Initial Firm Notification of Consignee or Public Letter
Distribution Pattern Nationwide Distribution.
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