Z-2235-2015 Class II Terminated
Recall Details
- Product Type
- Devices
- Report Date
- August 5, 2015
- Initiation Date
- February 11, 2015
- Termination Date
- December 30, 2015
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1
Product Description
Medical Device Exchange PT WIRE 300; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number 38931-04; EXP (repackager), Boston Scientific (OEM) Wire, guide, catheter
Reason for Recall
EXP did not register as a medical device establishment, list the devices being recalled, or establish its own quality system and instead relied on the fact that its vendors were registered and had their own quality systems.
Distribution Pattern
Distributed in DC and the states of CO, CA, FL, TX, and AR.
Code Information
OEM Catalog number 38931-04.