WOM World Of Medicine AG

FDA Regulatory Profile

WOM World Of Medicine AG appears in FDA public data with 5 recalls, 0 510(k) clearances, 5 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-2243-2024, Class II) was initiated on May 24, 2024.

Summary

Total Recalls
5
510(k) Clearances
0
Inspections
5
Compliance Actions
0

Known Names

wom world of medicine, w.o.m. world of medicine

Recent Recalls

NumberClassProductDate
Z-2243-2024Class IIWOM Tube Set for lrrlgatlon, single-use- Intended to transport irrigation fluid to the patient in enMay 24, 2024
Z-2629-2023Class IIAquilex Fluid Control System-Intended to provide fluid distension of the uterus during diagnostic anJuly 17, 2023
Z-2561-2021Class IICovidien HysteroLux Fluid Management System Control Unit, REF: 72205000June 18, 2021
Z-2767-2019Class IIAquilex Fluid Control System component: Bag deflector, REF AQL-100CBS Product Usage: Distends August 14, 2019
Z-0508-2019Class IIPNEUMOCLEAR Heated High-Flow Tube Set Product Usage: The Heated High-Flow Tube Set is a single October 22, 2018