BD DTX Plus, 60'' complete single-line pressure monitoring kit.
FDA Recall Z-1557-05 · Posted 2005-09-21
Recalling FirmBecton Dickinson Medical Systems
Recall StatusTerminated
Product CodeDXN
Date Initiated2005-07-01
Date Terminated2011-08-09
Product Quantity5470 units
Reason for Recall
Actuating tab may detach from the stopcock body, allowing fluid leak.
Firm Action
Consignees were notified by phone and fax on 07/01/2004.
Root Cause
Other
Distribution Pattern
Nationwide, including VA facilities in NY, SD, IL, OH and military facilities in GA, NC and Guam. Foreign distribution to 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.