WISSNER-BOSSERHOFF GMBH

FDA Regulatory Profile

WISSNER-BOSSERHOFF GMBH appears in FDA public data with 1 recall, 0 510(k) clearances, 1 FDA inspection, and 1 compliance action on record. Its most recent recall (Z-0329-2025, Class II) was initiated on July 11, 2022.

Summary

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

Recent Recalls

NumberClassProductDate
Z-0329-2025Class IISafeControl handset (a component of the Sentida bed which moves and positions the bed), Model NumberJuly 11, 2022