# FDA recall Z-1522-2022

> **Intera Oncology, Inc.** · Class I · device recall initiated 2022-07-10.

## Product

INTERA 3000 Hepatic Artery Infusion Pump, 30 mL, Sterile, Rx Only. implantable infusion pump.

## Reason for recall

Higher than expected flow rate.

## Distribution

US distribution to states of: AL, CA, IL, KY, MN, MO, NC, NJ, NY, OH, OR, PA, & TX.

## Key facts

- **Recall number:** Z-1522-2022
- **Recalling firm:** Intera Oncology, Inc.
- **Classification:** Class I
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-07-10
- **Report date:** 2022-08-31
- **Termination date:** 2023-09-12

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Wellesley, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1522-2022

## Citation

> AI Analytics. FDA recall Z-1522-2022. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1522-2022. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*