Recall Z-0795-2020— Riverpoint Medical, LLC
Class II · Terminated
Class II FDA medical device recall by Riverpoint Medical, LLC, initiated 2019-02-08, terminated 2021-04-28. FDA's recall record names no specific 510(k) clearance for this event. 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.. Reason: The integrity of the sterile grid packaging is potentially compromised..
- Recalling firm
- Riverpoint Medical, LLC
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2019-02-08
- Terminated
- 2021-04-28
- Firm location
- Portland, OR, United States
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.
Reason for recall
The integrity of the sterile grid packaging is potentially compromised.
Data sourced from openFDA. This site is unofficial and independent of the FDA.