Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
INTERA 3000 Hepatic Artery Infusion Pump Recalled by Intera Oncology, Inc. Due to Higher than expected flow rate.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Intera Oncology, Inc. directly.
Affected Products
INTERA 3000 Hepatic Artery Infusion Pump, 30 mL, Sterile, Rx Only. implantable infusion pump.
Quantity: 50 units
Why Was This Recalled?
Higher than expected flow rate.
Where Was This Sold?
This product was distributed to 13 states: AL, CA, IL, KY, MN, MO, NJ, NY, NC, OH, OR, PA, TX
About Intera Oncology, Inc.
Intera Oncology, Inc. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report