Riverpoint Medical, LLC: Medical Device Recall in 2019 - (Recall #: Z-0777-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

RP RIVERPOINT MEDICAL 18G Brachy Grid B&K(TM) style, REF RPG-18 Product Usage: The Riverpoint Brachytherapy Grid is used during Brachytherapy procedures to assist with the precise insertion of the needle or other probes. The Riverpoint Brachytherapy Grid is placed against the skin of the patient to help the user place the needles in a grid pattern. The letters and numbers can also correspond with computerized grids to aid in placement.

Product Classification:

Class III

Date Initiated: January 9, 2018

Date Posted: February 6, 2019

Recall Number: Z-0777-2019

Event ID: 81935

Reason for Recall:

Product is labeled with "CE", but is not yet approved in the European Union.

Status: Terminated

Product Quantity: 443 devices

Code Information:

Lot Numbers: 18061816, 18101521

Distribution Pattern:

US Nationwide Distribution in the states of IL, WA, and FL

Voluntary or Mandated:

Voluntary: Firm initiated