FDA Medical Device Recalls (openFDA)
Riverpoint Medical, LLC: 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.
- Recall number
- Z-0795-2020
- Recalling firm
- Riverpoint Medical, LLC
- 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.
- Status
- Terminated
- Initiated
- 2019-02-08
- Posted
- 2020-01-10
- Terminated
- 2021-04-28
- Reason
- The integrity of the sterile grid packaging is potentially compromised.
- Root cause
- Packaging
- Action
- Recall notifications dated 2/8/2019 were issued via email and overnight mail on 2/8/2019.
- Quantity
- 3,234 devices
- Distribution
- Distribution was made to IL, FL, TX, and WA. There was no foreign/military/government distribution.
- Lot, serial or model codes
- Lot numbers 16032422, 16051814, 16051815, 16052425, 17042430, 17050936, 17052532, 17061214, 17121823, 17122820, 18040922, 18061816, 18101521, and 18120705; UDI number 00812444028638.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- IWJ
- Firm FEI
- 3006981798
- Firm city
- Portland
- Firm state
- OR
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28