WillowWood Global Llc

FDA Regulatory Profile

WillowWood Global Llc appears in FDA public data with 1 recall, 0 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1594-2021, Class II) was initiated on April 20, 2021.

Summary

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

Recent Recalls

NumberClassProductDate
Z-1594-2021Class IIAlpha Interlock Suspension System Lanyard Body: An external prosthetic device. The Alpha Lanyard incApril 20, 2021