Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
RP RIVERPOINT MEDICAL 18G Brachy Grid B&K(TM) style Recalled by Riverpoint Medical, LLC Due to Product is labeled with "CE", but is not...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Riverpoint Medical, LLC directly.
Affected Products
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.
Quantity: 443 devices
Why Was This Recalled?
Product is labeled with "CE", but is not yet approved in the European Union.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Riverpoint Medical, LLC
Riverpoint Medical, LLC has 47 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report