Martin Bauer, Inc.

FDA Regulatory Profile

Martin Bauer, Inc. has 1 FDA recall, 9 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest recall
H-0532-2025 · Class II · Jul 22, 2025
Latest inspection
Jul 20, 2026 · NAI

Reviewing Martin Bauer, Inc. as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Check this supplier

Or check Martin Bauer, Inc. yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.

Get a free API key

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls1Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections9Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Related names

NameRecalls510(k)InspectionsComplianceMost recent recall
Martin Bauer Gmbh And Co. Kg
Same company group
0020—

Recent Recalls

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

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 20, 2026Islandia, NYFood/CosmeticsNo Action Indicated (NAI)3004255622
Jun 13, 2025Secaucus, NJFood/CosmeticsNo Action Indicated (NAI)3012322560
Sep 7, 2021Islandia, NYFood/CosmeticsNo Action Indicated (NAI)3004255622
Oct 21, 2020Secaucus, NJFood/CosmeticsNo Action Indicated (NAI)3012322560
Jun 5, 2018Islandia, NYFood/CosmeticsNo Action Indicated (NAI)3004255622
May 18, 2018Secaucus, NJFood/CosmeticsVoluntary Action Indicated (VAI)3012322560
Feb 10, 2017Nichelino, ItalyFood/CosmeticsNo Action Indicated (NAI)3006556501
Apr 14, 2015Islandia, NYFood/CosmeticsNo Action Indicated (NAI)3004255622
Aug 9, 2010Islandia, NYFood/CosmeticsVoluntary Action Indicated (VAI)3004255622

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 3004255622Islandia, NY5Jul 20, 2026
FEI 3012322560Secaucus, NJ3Jun 13, 2025
FEI 3006556501Nichelino, Italy1Feb 10, 2017

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.