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FDA device recall Z-2304-2011 · posted 2011-05-27 · Terminated

Recall details

Recalling firm
Centurion Medical Products Corporation
Reason for recall
This voluntary sub-recall was initiated because the vials of Bacteriostatic Sodium Chloride Injection, USP, 0.9% utilized to make the products may contain visible particulates.
Action taken
Centurion Medical Products Corporation issued press on April 1, 2011, and sent an Urgent Voluntary Recall letter dated March 15, 2011, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to discontinue use of the kits immediately and instructions were provided for the return of the kits. Customers were also asked to complete a form to fax or email back to the firm regarding the number of kits the firm has in their possession. Customers were instructed to provide recall notification to other firm's who received the recalled kits from their direct account. For any questions regarding this recall call 631-924-4000, ext 142.
Root cause
Material/Component Contamination
Status
Terminated
Product code
LRS
Quantity affected
390
Distribution
Nationwide Distribution
Date initiated
2011-03-31
Date posted
2011-05-27
Date terminated
2011-09-13
Location
Williamston, MI

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