16 G / 5F Dual Lumen L-Cath catheter only.
FDA Recall Z-0282-06 · Posted 2005-12-15
Recalling FirmBecton Dickinson Medical Systems
Recall StatusTerminated
Product CodeLJS
Date Initiated2005-03-25
Date Terminated2011-08-08
Product Quantity8090 units
Reason for Recall
Aspiration (blood return) could not be achieved on some L-Cath 16 gauge catheters.
Firm Action
Consignees were notified via telephone and fax letter, beginning 04/25/2005.
Root Cause
Other
Distribution Pattern
AL, CA, CO, FL, GA, IL, IN, KY, LA, MA, MD, MI, MN, NJ, OH, OK, PA, TN, TX, WA. No Government or military consignees. Foreign distribution to Australia, Canada, Japan.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.