BUNGE NORTH AMERICA INC FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

BUNGE NORTH AMERICA INC has 1 FDA recall, 21 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "BUNGE NORTH AMERICA INC" is on file.

What these totals cover: FDA records filed under the name "BUNGE NORTH AMERICA INC" and its spelling variant "Bunge North America".

Latest recall
H-0354-2025 · Class II · Jul 14, 2025
Latest inspection
Nov 13, 2025 · NAI

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
Inspections21Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

BUNGE NORTH AMERICA INC's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

BUNGE NORTH AMERICA INC: FDA inspections per year 2017: 3 inspections320172018: 1 inspections120182019: 1 inspections120192020: 0 inspections020202021: 1 inspections120212022: 0 inspections020222023: 0 inspections020232024: 2 inspections220242025: 2 inspections220252026: 0 inspections02026
YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202520010
202420000
202300000
202200000
202110000
202000000
201910000
201810000
201730000

Inspections are counted by the date they ended, warning letters by the date FDA issued them and recall records by the recall start date. FDA lists one recall record per recalled product, so one recall event can add several.

Reviewing BUNGE NORTH AMERICA 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 BUNGE NORTH AMERICA 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

Recent recalls

1 recall record on Jul 14, 2025.

NumberClassProductDate
H-0354-2025Class IINH EUROPEAN STYLE BUTTER BLEND, BUNGE, NET WT 1 LB, MFD IN USA BY: Bunge Oils, Chesterfield, MO…Jul 14, 2025

Recent FDA inspections

21 inspections from Jun 20, 2012 to Nov 13, 2025. Showing the 20 most recent. View all 21 inspections

DateSiteProductClassificationFEI
Nov 13, 2025Gibson City, ILFood/CosmeticsNo Action Indicated (NAI)3000718480
Apr 15, 2025Saint Charles, MOFood/CosmeticsNo Action Indicated (NAI)3013639068
Oct 30, 2024Remington, INFood/CosmeticsNo Action Indicated (NAI)3009891804
Feb 21, 2024Dyersburg, TNFood/CosmeticsNo Action Indicated (NAI)1029689
Dec 1, 2021Saint Charles, MOFood/CosmeticsNo Action Indicated (NAI)3013639068
Sep 5, 2019Hickman, KYFood/CosmeticsNo Action Indicated (NAI)3004292225
Feb 26, 2018Gibson City, ILFood/CosmeticsNo Action Indicated (NAI)3009726923
Oct 6, 2017Memphis, TNFood/CosmeticsNo Action Indicated (NAI)3004292777
Sep 19, 2017Lettsworth, LAFood/CosmeticsNo Action Indicated (NAI)2317712
Aug 25, 2017Vidalia, LAFood/CosmeticsVoluntary Action Indicated (VAI)3004292175
Nov 7, 2016Dyersburg, TNFood/CosmeticsNo Action Indicated (NAI)1029689
Aug 11, 2016Mayersville, MSFood/CosmeticsNo Action Indicated (NAI)1025671
Apr 5, 2016Waterloo, INFood/CosmeticsNo Action Indicated (NAI)1818880
Oct 15, 2015Hull, ILFood/CosmeticsNo Action Indicated (NAI)3004292030
Jul 9, 2015Remington, INFood/CosmeticsNo Action Indicated (NAI)3009891804
Jul 8, 2015Remington, INFood/CosmeticsNo Action Indicated (NAI)3009891804
Mar 16, 2015Hickman, KYVeterinaryNo Action Indicated (NAI)3004292225
Apr 23, 2013Mayersville, MSFood/CosmeticsNo Action Indicated (NAI)3010171538
Mar 11, 2013Memphis, TNFood/CosmeticsNo Action Indicated (NAI)3004292777
Nov 8, 2012Cincinnati, OHFood/CosmeticsNo Action Indicated (NAI)1514954
NAI
No objectionable conditions or practices were found during the inspection.
VAI
Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI
Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-inspected facilities

15 inspected sites, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3000718480Gibson City, IL1Nov 13, 2025
FEI 3013639068Saint Charles, MO2Apr 15, 2025
FEI 3009891804Remington, IN3Oct 30, 2024
FEI 1029689Dyersburg, TN2Feb 21, 2024
FEI 3004292225Hickman, KY2Sep 5, 2019
FEI 3009726923Gibson City, IL1Feb 26, 2018
FEI 3004292777Memphis, TN2Oct 6, 2017
FEI 2317712Lettsworth, LA1Sep 19, 2017
FEI 3004292175Vidalia, LA1Aug 25, 2017
FEI 1025671Mayersville, MS1Aug 11, 2016
FEI 1818880Waterloo, IN1Apr 5, 2016
FEI 3004292030Hull, IL1Oct 15, 2015
FEI 3010171538Mayersville, MS1Apr 23, 2013
FEI 1514954Cincinnati, OH1Nov 8, 2012
FEI 1453125Gibson City, IL1Jun 20, 2012

BUNGE NORTH AMERICA INC and the FDA: common questions

Has BUNGE NORTH AMERICA INC received an FDA warning letter?

No FDA warning letter addressed to the name "BUNGE NORTH AMERICA INC" is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has BUNGE NORTH AMERICA INC received an FDA Form 483?

FDA has not published a Form 483 for "BUNGE NORTH AMERICA INC" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect BUNGE NORTH AMERICA INC?

The most recent FDA inspection on file ended Nov 13, 2025 at Gibson City, IL and was classified NAI. FDA has 21 inspections of BUNGE NORTH AMERICA INC on file.

Has BUNGE NORTH AMERICA INC had an FDA recall?

Yes. BUNGE NORTH AMERICA INC has 1 FDA recall on record. The most recent started Jul 14, 2025.

Need more than this page shows? Ask about BUNGE NORTH AMERICA INC in Claude or ChatGPT and get every site's inspections, Form 483s, warning letters and import alerts, with a link to the FDA source for each record. The API key is free: no card.

Get a free API key

Prefer a PDF? Request a free supplier snapshot.

Is this your company or a supplier you list? Link to this FDA record from your site with a free button.

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