Device recall

Z-0795-2020: Riverpoint Medical 18G Brachy Grid, B&K style, REF RPG-18, Sterile, Rx. The firm…

FDA device recall · Class II · Riverpoint Medical, LLC

Key facts

Recall number (Z-number) Z-0795-2020
Recall event 84528
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.
Product code IWJ
Recalling firm Riverpoint Medical, LLC
Recall class Class II
Status Terminated
Termination date Apr 28, 2021
FEI number 3006981798

At a glance

  • None Linked 510(k)s
  • 1–9 Products in the same recall event
  • 10–99 Recalled products with this product code

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device recalls (products)

Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.

Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database

Browse all FDA device recalls (products)