Z-1561-05

BD DTX Plus, 12'' single-line neonatal pressure monitoring kit

Name: Z-1561-05 BD DTX Plus, 12'' single-line neonatal pressure monitoring kit
Creator: Becton Dickinson Medical Systems
Published: 2005-07-01
License: https://open.fda.gov/license/

Becton Dickinson Infusion Therapy Systems Inc. / initiated 2005-07-01 / Terminated

FDA source

Becton Dickinson Medical Systems began a recall of BD DTX Plus, 12'' single-line neonatal pressure monitoring kit on 2005-07-01. The reason FDA records is "Actuating tab may detach from the stopcock body, allowing fluid leak". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-1561-05
Status: Terminated
Initiated: 2005-07-01
Posted: 2005-09-21
Terminated: 2011-08-09
Recalling firm: Becton Dickinson Infusion Therapy Systems Inc.
Product: BD DTX Plus, 12'' single-line neonatal pressure monitoring kit.
Product code: DXN System, Measurement, Blood-Pressure, Non-Invasive
Reason for recall: Actuating tab may detach from the stopcock body, allowing fluid leak.
FDA root cause: Other
Action: Consignees were notified by phone and fax on 07/01/2004.
Quantity in commerce: 1060 units
Distribution: Nationwide, including VA facilities in NY, SD, IL, OH and military facilities in GA, NC and Guam. Foreign distribution to Japan.
Product codes and lots: Part number 682040, Part numbers 407033, 408053.

Product code DXN

K935782Class IIDtx and Dtx Plus Disposable Pressure Transducers and AccessoriesOhmeda Medical / cleared 1994-08-01

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)