Medrad Inc Veris Invasive Blood Pressure Interface Cables-Part # 3010478. The product is an accessory to patient physiological monitor. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Veris Invasive Blood Pressure Interface Cables-Part # 3010478. The product is an accessory to patient physiological monitor.
Brand
Medrad Inc
Lot Codes / Batch Numbers
Catalog number 3010478
Products Sold
Catalog number 3010478
Medrad Inc is recalling Veris Invasive Blood Pressure Interface Cables-Part # 3010478. The product is an accessory to patie due to Interference problems: certain invasive blood pressure transducers connected to these cables are susceptible to interference if exposed to static magn. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, CO, HI, IL, IN, MD, MA, NJ, NY, OH, PA, TX, WA
Page updated: Jan 10, 2026