KAYSERBETTEN GMBH & CO. KG

FDA Regulatory Profile

KAYSERBETTEN GMBH & CO. KG appears in FDA public data with 1 recall — including 1 Class I (most serious) —, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-2212-2026, Class I) was initiated on May 4, 2026.

Summary

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

Recent Recalls

NumberClassProductDate
Z-2212-2026Class IPediatric care bed; Product Designation: KayserBett IDA;May 4, 2026