RP Riverpoint Medical recall
RP RIVERPOINT MEDICAL 18G Brachy Grid B&K(TM) style, REF RPG-18 Product Usage: The Riverpoint Brachytherapy Grid is used during Brachytherapy…
Why was RP Riverpoint Medical recalled?
Product is labeled with "CE", but is not yet approved in the European Union.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot Numbers: 18061816, 18101521
- Product
- RP RIVERPOINT MEDICAL 18G Brachy Grid B&K(TM) style, REF RPG-18 Product Usage: The Riverpoint Brachytherapy Grid is used during Brachytherapy…
- Recalling firm
- Riverpoint Medical, LLC
- Quantity
- 443 devices
- Distribution
- US Nationwide Distribution in the states of IL, WA, and FL
- Recall date
- February 6, 2019
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)