Riverpoint Medical, LLC: Medical Device Recall in 2020 - (Recall #: Z-0795-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: February 8, 2019

Date Posted: January 22, 2020

Recall Number: Z-0795-2020

Event ID: 84528

Reason for Recall:

The integrity of the sterile grid packaging is potentially compromised.

Status: Terminated

Product Quantity: 3,234 devices

Code Information:

Lot numbers 16032422, 16051814, 16051815, 16052425, 17042430, 17050936, 17052532, 17061214, 17121823, 17122820, 18040922, 18061816, 18101521, and 18120705; UDI number 00812444028638.

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated