Wellesley, MA, United States
Intera Oncology, Inc. recalls
1 recall recorded since 2018, most recently on 10 July 2022. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)1
Terminated Class I Medical devices
- Recall started
- 10 July 2022
- Terminated
- 12 September 2023
- Reason
- Higher than expected flow rate.
- Distribution
- US distribution to states of: AL, CA, IL, KY, MN, MO, NC, NJ, NY, OH, OR, PA, & TX.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-1522-2022
- INTERA 3000 Hepatic Artery Infusion Pump, 30 mL, Sterile, Rx Only. implantable infusion pump.
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.