Z-0259-2007

Veris Invasive Blood Pressure Interface Cables-Part # 3010478. The product is an accessory to patient...

Name: Z-0259-2007 Veris Invasive Blood Pressure Interface Cables-Part # 3010478. The product is an accessory to patient...
Creator: Medrad Inc
Published: 2006-09-29
License: https://open.fda.gov/license/

Medrad, Inc. / initiated 2006-09-29 / Terminated

FDA source

Medrad Inc began a recall of Veris Invasive Blood Pressure Interface Cables-Part # 3010478. The product is an accessory to patient physiological monitor on 2006-09-29. The reason FDA records is "Interference problems: certain invasive blood pressure transducers connected to these cables are susceptible to interference if exposed to static magnetic field strengths exceeding 300 gauss. In certain orientations...". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0259-2007
Status: Terminated
Initiated: 2006-09-29
Posted: 2006-12-15
Terminated: 2007-06-20
Recalling firm: Medrad, Inc.
Product: Veris Invasive Blood Pressure Interface Cables-Part # 3010478. The product is an accessory to patient physiological monitor.
Product code: MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
Reason for recall: Interference problems: certain invasive blood pressure transducers connected to these cables are susceptible to interference if exposed to static magnetic field strengths exceeding 300 gauss. In certain orientations, the transducer causes the invasive blood pressure readings on the physiological monitor to display inaccurate readings.
FDA root cause: Other
Action: The recalling firm contacted all affected customers via telephone or letter dated November 20, 2006 to inform them of the problem and instruct them to return the cables or apply corrective labeling.
Quantity in commerce: 80 units
Distribution: Worldwide distribution ---- including USA state of CA, CO, HI, IL, IN, MA, MD, NJ, NY, OH, PA, TX, and WA and countries of The Netherlands, Denmark, Australia, Brazil, Italy, and Japan.
Product codes and lots: Catalog number 3010478

Product code MWI

K042569Class II8600 Vital Signs MonitorCriticare Systems, Inc. / cleared 2004-09-29

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)