Kadesh International

FDA Regulatory Profile

Kadesh International appears in FDA public data with 1 recall — including 1 Class I (most serious) —, 0 510(k) clearances, 2 FDA inspections, and 1 compliance action on record. Its most recent recall (D-0250-2019, Class I) was initiated on November 5, 2018.

Summary

Total Recalls
1 (1 Class I)
510(k) Clearances
0
Inspections
2
Compliance Actions
1

Recent Recalls

NumberClassProductDate
D-0250-2019Class Ipuriton EYE RELIEF DROPS, 0.5 oz (15 ml) bottle, Kadesh Inc., NDC#7079600115, UPC 7 36972 16799 0.November 5, 2018