PlainRecalls
FDA Devices Moderate Class II Terminated

Iced Thermoset Closed-Loop Injectate Delivery System for cold Injectate. 1 unit per Cavity #6x12x2.6 Cav/10 pieces per case R1-6090

Reported: January 2, 2019 Initiated: October 5, 2018 #Z-0662-2019

Product Description

Iced Thermoset Closed-Loop Injectate Delivery System for cold Injectate. 1 unit per Cavity #6x12x2.6 Cav/10 pieces per case R1-6090

Reason for Recall

Potential for leakage due to defect in the thermoset check valve component.

Details

Recalling Firm
ICU Medical, Inc.
Units Affected
1,760 units
Distribution
United States - AL, CA, CO, DC, FL, GA, IN, KY, LA, MA, ME, MD, MI, MO, MS, MT, NJ, NY, NC, OH, OK, OR, PA, SC, TN, TX, VA, WA, WI, WV, WY
Location
San Clemente, CA

Frequently Asked Questions

What product was recalled?
Iced Thermoset Closed-Loop Injectate Delivery System for cold Injectate. 1 unit per Cavity #6x12x2.6 Cav/10 pieces per case R1-6090. Recalled by ICU Medical, Inc.. Units affected: 1,760 units.
Why was this product recalled?
Potential for leakage due to defect in the thermoset check valve component.
Which agency issued this recall?
This recall was issued by the FDA Devices on January 2, 2019. Severity: Moderate. Recall number: Z-0662-2019.