Bruder Healthcare Company, LLC

FDA Regulatory Profile

Bruder Healthcare Company, LLC appears in FDA public data with 9 recalls, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1361-2024, Class II) was initiated on February 21, 2024.

Summary

Total Recalls
9
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Known Names

bruder healthcare company, bruder healthcare

Recent Recalls

NumberClassProductDate
Z-1361-2024Class IIThermalon Sinus Compress, Item Number 24332February 21, 2024
Z-1365-2024Class IIThermalon Stye Compress, Item Number 24352February 21, 2024
Z-1367-2024Class IIMediBeads King Pad, Item Numbers: 34120, 34120PM, 34125RFebruary 21, 2024
Z-1360-2024Class IIThermalon Sinus Compress (French), Item Number 24332FFebruary 21, 2024
Z-1359-2024Class IIThermalon Eye Compress, Item Number 2434February 21, 2024
Z-1366-2024Class IIMediBeads Neck Wrap, Item Number 34320February 21, 2024
Z-1363-2024Class IIThermalon Neck Wrap, Item Number 24322February 21, 2024
Z-1362-2024Class IIThermalon Back Wrap, Item Number 24312February 21, 2024
Z-1364-2024Class IIThermalon Heating Pad, Item Number 24002February 21, 2024