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
FDA Recall Z-1070-2019 · Posted None
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Recalling FirmICU Medical, Inc.
Recall StatusTerminated
Product CodeDRS
Date Initiated2018-11-27
Date Terminated2022-02-01
Product Quantity5000
Reason for Recall
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.
Firm 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.
Root Cause
Process design
Distribution Pattern
U.S.: CA, TX, WI, NY, NC, GA, PA, and NY. Foreign: Canada
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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