# FDA recall Z-0795-2020

> **Riverpoint Medical, LLC** · Class II · device recall initiated 2019-02-08.

## Product

Riverpoint Medical 18G Brachy Grid, B&K style, REF RPG-18, Sterile, Rx.  The firm name on the label is Riverpoint Medical, LLC, Portland, OR.

## Reason for recall

The integrity of the sterile grid packaging is potentially compromised.

## Distribution

Distribution was made to IL, FL, TX, and WA.  There was no foreign/military/government distribution.

## Key facts

- **Recall number:** Z-0795-2020
- **Recalling firm:** Riverpoint Medical, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-02-08
- **Report date:** 2020-01-22
- **Termination date:** 2021-04-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Portland, OR, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0795-2020

## Citation

> AI Analytics. FDA recall Z-0795-2020. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0795-2020. Source: US FDA. Licensed CC0.

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