Riverpoint Medical 18G Brachy Grid — Class II medical device recall Z-0795-2020
Terminated recall by Riverpoint Medical, LLC, reported 2020-01-22, distributed in FL, IL, TX, WA. The integrity of the sterile grid packaging is potentially compromised.
| Recall number | Z-0795-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Riverpoint Medical, LLC, Portland, OR, United States |
| Recall initiated | 2019-02-08 |
| Classified | 2020-01-10 |
| Reported by FDA | 2020-01-22 |
| Terminated | 2021-04-28 |
| Distributed | FL, IL, TX, WA |
| Quantity | 3,234 devices |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 00812444028638 |
| Lot numbers | 16032422, 16051814, 16051815, 16052425, 17042430, 17050936, 17052532, 17061214, 17121823, 17122820, 18040922, 18061816, 18101521, 18120705 |
| Model numbers | RPG-18 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0795-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.