Martin Bauer, Inc.

FDA Regulatory Profile

Martin Bauer, Inc. appears in FDA public data with 1 recall, 0 510(k) clearances, 9 FDA inspections, and 0 compliance actions on record. Its most recent recall (H-0532-2025, Class II) was initiated on July 22, 2025.

Summary

Total Recalls
1
510(k) Clearances
0
Inspections
9
Compliance Actions
0

Recent Recalls

NumberClassProductDate
H-0532-2025Class IIPassionflower Herb Powdered Extract 4%, bulk packaging, individual large box, corrugated cardboard bJuly 22, 2025