PlainRecalls
FDA Devices Moderate Class II Terminated

Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as Primary PLUM Set 0.2 Micron Filter, Prepierced Y-Site, Polyethylene Lined Light Resistant Tubing, Distal Microbore Tubing, Secure Lock, 104 Inch. 1 unit per pouch; 50 pouches per case

Reported: October 23, 2019 Initiated: July 29, 2019 #Z-0127-2020

Product Description

Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as Primary PLUM Set 0.2 Micron Filter, Prepierced Y-Site, Polyethylene Lined Light Resistant Tubing, Distal Microbore Tubing, Secure Lock, 104 Inch. 1 unit per pouch; 50 pouches per case

Reason for Recall

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

Details

Recalling Firm
ICU Medical Inc
Units Affected
78,877 units
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.
Location
Lake Forest, IL

Frequently Asked Questions

What product was recalled?
Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as Primary PLUM Set 0.2 Micron Filter, Prepierced Y-Site, Polyethylene Lined Light Resistant Tubing, Distal Microbore Tubing, Secure Lock, 104 Inch. 1 unit per pouch; 50 pouches per case. Recalled by ICU Medical Inc. Units affected: 78,877 units.
Why was this product recalled?
Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.
Which agency issued this recall?
This recall was issued by the FDA Devices on October 23, 2019. Severity: Moderate. Recall number: Z-0127-2020.