FDA Recall Terminated

ICU Medical, Transpac IV Monitoring Kit With Safeset Reservoir and Blood Sampling Port, 60" Tubing, Disposable Transducer, 3 ml Squeeze Flush, Macrodrip (Pole Mount), REF: 42640-06, Sterile EO

Recall: Z-1071-2019 · Initiated November 27, 2018

Recall

Recall Number
Z-1071-2019
Event Number
81743
Firm
ICU Medical, Inc.
FEI Number
2025816
Product Code
DRS
Status
Terminated
Root Cause
Process design
Initiated
November 27, 2018
Terminated
February 1, 2022
Address
951 Calle, Amanecer San Clemente, CA, 92673-6212

Description

ICU Medical, Transpac IV Monitoring Kit With Safeset Reservoir and Blood Sampling Port, 60" Tubing, Disposable Transducer, 3 ml Squeeze Flush, Macrodrip (Pole Mount), REF: 42640-06, Sterile EO

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.

Action

On 11/27/18, Urgent Medical Device Recall notices were sent via traceable mailing to customers informing them to discontinue use and distribution of the affected product. In addition, customers were asked to quarantine and return affected product, and to complete and return response forms. Customers were instructed to inform all potential users of the product within their organization, and if the product had been further distributed, to immediately notify these additional customers. Customers with additional questions were encouraged to call: Global Complaint Management @ 1-844-654-7780 ([email protected]), Medical Information @ 1-800-241-4002 option 6 ([email protected]), or Customer Care @ 1-949-366-4208.

Distribution

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

Quantity

280