Lymol Medical

FDA Regulatory Profile

Lymol Medical appears in FDA public data with 1 recall, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (D-0858-2016, Class II) was initiated on April 28, 2016.

Summary

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

Recent Recalls

NumberClassProductDate
D-0858-2016Class IISclerosol Intrapleural Aerosol (sterile talc powder), Intrapleural administration, 4 g Canister, Rx April 28, 2016