V-CATH Insertion Kits, Sterile; Product Code Number: 301-00; Manufactured by Centurion Medical Products for Neo Medical; 42514 Albrae Street, Fremont, CA 94538
FDA Recall Z-2223-2011 · Posted 2011-05-19
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Recalling FirmNeo Medical, Inc.
Recall StatusTerminated
Product CodeLRS
Date Initiated2011-04-05
Date Terminated2011-11-22
Product Quantity1990
Reason for Recall
Firm received recall notice from their contract manufacturer due to visible particulates in Bacteriostatic Sodium Chloride Injection, USP 0.9%, 30 mL vials that are included in insertion kits.
Firm Action
Neo Medical forwarded Urgent Recall Notices to Dealers and customers on April 5, 2011 via fax. Neo Medical Customer Care also contacted customers by phone on April 7, 2011, followed by Urgent Product Recall Notification letters were sent on April 11, 2011 along with a copy of the Recall Notification from Centurion. The letter requested that customers with affected lots immediately discontinue distribution and contact the end users instructing them to stop dispensing the product. Customers were to complete the accountability information even if inventory had been depleted and fax it to 510-353-9025. In order to return the affected product, customers should contact the Complaint Coordinator at 925-719-2197 or [email protected]. Replacement or credit would be issued for all product returned.
Root Cause
Material/Component Contamination
Distribution Pattern
Worldwide Distribution -- USA, including states of MO, WA, PA, CA, OH, UT, TX and Canada.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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