Skip to content
Recall Observatory FDA recall evidence

Device product

ICU Medical, Transpac IV Monitoring Kit With Safeset Reservoir and Blood Sampling Port, 152 cm (60") Tubing, Disposable Transducer, 03 ml Squeeze Flush Device, Macrodrip (Pole Mount), REF: 01C-42640-06, Sterile EO

Z-1070-2019

November 27, 2018

Class II

Product summary

Firm
ICU Medical, Inc.
Event
Event 81743
Status
Terminated
Classification
Class II
Quantity
5000
Official record key
device-enforcement:Z-1070-2019

Official wording

Reason: Reports of pressure tubing separation between the sampling port and the high pressure tubing on certain lots of extravascular blood pressure transducers, which could lead to delay in therapy, and in rare circumstances, pressure tubing separations could lead to blood loss, air embolism, or contamination of the fluid path.

Code information: Lot/UDI: 3514084/ (01)0 0840619 03747 5 (17) 201001 (30) 01 (10) 3514084; 3550279/ (01)0 0840619 03747 5 (17) 201001 (30) 01 (10) 3550279

Distribution pattern: U.S.: CA, TX, WI, NY, NC, GA, PA, and NY. Foreign: Canada

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Reports of pressure tubing separation between the sampling port and the high pressure tubing on certain lots of extravascular blood pressure transducers, which could lead to delay in therapy, and in rare circumstances, pressure tubing separations could lead to blood loss, air embolism, or contamination of the fluid path.