Gardner Denver Thomas Inc

FDA Regulatory Profile

Gardner Denver Thomas Inc appears in FDA public data with 3 recalls, 0 510(k) clearances, 4 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-2150-2015, Class II) was initiated on June 4, 2015.

Summary

Total Recalls
3
510(k) Clearances
0
Inspections
4
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-2150-2015Class IITHOMAS by Gardner Denver, MEDI-PUMP(R) Aspirator, Model 1242 Product Usage: medical aspiratorJune 4, 2015
Z-2149-2015Class IITHOMAS by Gardner Denver, MEDI-PUMP(R) Aspirator, Model 1240 Product Usage: medical aspiratorJune 4, 2015
Z-2151-2015Class IITHOMAS by Gardner Denver, MEDI-PUMP(R) Aspirator, Model 1243 Product Usage: medical aspiratorJune 4, 2015