FDA Enforcement Class II Terminated

Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Epidural Set Yellow-Striped Microbore, 0.2 Micron Filter, PAV 123 inch. 1 unit per pouch; 50 pouches per case

Recall: Z-0132-2020 · Reported October 23, 2019

Enforcement

Recall Number
Z-0132-2020
Event ID
83549
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
ICU Medical Inc
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
October 23, 2019
Initiation Date
July 29, 2019
Classification Date
October 14, 2019
Termination Date
January 12, 2024
Address
600 N Field Dr, N/A, Lake Forest, IL, 60045-4835, United States

Description

Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Epidural Set Yellow-Striped Microbore, 0.2 Micron Filter, PAV 123 inch. 1 unit per pouch; 50 pouches per case

Reason

Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.

Code Info

Product Code: 163730455, Lot number (UDI Number): 896225H (20887787007408, 10887787007401), 916845H (20887787007408, 10887787007401), 925825H (20887787007408, 10887787007401), 948155H (20887787007408, 10887787007401)

Distribution

Nationwide distribution to AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VI, VT, WA, WI, WV, WY. International distribution to Canada, Chile, France, Germany, Greece, Hong Kong, Ireland, Italy, Oman, Philippines, Poland, Saudi Arabia, South Africa, Spain, Taiwan, Turkey, United Arab Emirates, United Kingdom.

Quantity

26,700 units