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Intera Oncology, Inc. recalls INTERA 3000 Hepatic Artery Infusion Pump, 30 mL, Sterile, Rx Only. implantable infusion pump.
Recalled August 31, 2022 · FDA recall Z-1522-2022 · Intera Oncology
Hazard
Higher than expected flow rate. · FDA Class I
Units
50 units
Sold at
US distribution to states of: AL, CA, IL, KY, MN, MO, NC, NJ, NY, OH, OR, PA, & TX.
Description
Higher than expected flow rate.
Product
INTERA 3000 Hepatic Artery Infusion Pump, 30 mL, Sterile, Rx Only. implantable infusion pump.
Manufacturer(s)
Intera Oncology, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →