Class II
Medical Device Recall: Regard Kit containing the Microtek decanter
ROi CPS LLC · June 17, 2024
Reason for Recall
Decanters may have pin holes and tears in sterile packaging that cannot be identified visually.
Distribution
US Nationwide distribution in the state of MO.
States Affected
NATIONWIDE
Quantity Affected
78 Kits
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2685-2024
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.