FDA Recall Terminated

MEDRAD Hand Controller Sheath, Catalog number AVA 500 HCS/3010903, for cardiac catheterization procedures. The Sterile Sheath is specifically intended for use in the x-ray angiography environment to cover the Medrad Avanta Sterile Hand Controller to prevent cross contamination between patients.

Recall: Z-0870-2013 · Initiated November 5, 2012

Recall

Recall Number
Z-0870-2013
Event Number
64329
Firm
Medrad Inc
FEI Number
3006316319
Product Code
DXT
Status
Terminated
Root Cause
Packaging
Initiated
November 5, 2012
Posted
February 21, 2013
Terminated
March 10, 2015
Address
100 Global View Dr, Warrendale, PA, 15086

Description

MEDRAD Hand Controller Sheath, Catalog number AVA 500 HCS/3010903, for cardiac catheterization procedures. The Sterile Sheath is specifically intended for use in the x-ray angiography environment to cover the Medrad Avanta Sterile Hand Controller to prevent cross contamination between patients.

Reason

The seal between the white polyethylene and the clear plastic may be missing on the Hand Controller Sheath package, resulting in a potential breach of the sterility of this accessory.

Action

Medrad sent a Recall letter dated November 5, 2012, to all affected customers. The letter identified the product the problem and the action needed to be taken by the customer. Customer were instructed to review their inventory and quarantine any packages with an expiration date prior to April, 2017. Customers were also given the option of conducting a visual inspection on site to determine if the product should be returned. Alternatively, the customer has the option of returning the affected product. If the customer has affected product, they are instructed to contact Medrad Customer Support to make arrangements for the return and replacement of the product. For further questions please call our Customer Support Team at 1-877-229-3767.

Distribution

Worldwide Distribution including USA nationwide.

Quantity

832,175