Teva Pharmaceutical Industries

FDA Regulatory Profile

Teva Pharmaceutical Industries appears in FDA public data with 1 recall, 0 510(k) clearances, 15 FDA inspections, and 1 compliance action on record. Its most recent recall (D-0521-2016, Class III) was initiated on October 20, 2015.

Summary

Total Recalls
1
510(k) Clearances
0
Inspections
15
Compliance Actions
1

Recent Recalls

NumberClassProductDate
D-0521-2016Class IIIIrbesartan and Hydrochlorothiazide tablets USP 150 mg/ 12.5 mg, 90-count bottles, Rx only, ManufactuOctober 20, 2015