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Terminated

BD DTX Plus, 60'' complete dual-line pressure monitoring kit.

FDA Recall Z-1558-05 · Posted 2005-09-21

Recalling FirmBecton Dickinson Medical Systems
Recall StatusTerminated
Product CodeDXN
Date Initiated2005-07-01
Date Terminated2011-08-09
Product Quantity95 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.

K935782DTX AND DTX PLUS DISPOSABLE PRESSURE TRANSDUCERS AND ACCESSORIESOhmeda Medical · 1994-08-01

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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