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BASF Corporation

FDA Regulatory Profile

BASF Corporation has 1 FDA recall, 31 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest recall
D-0149-2021 · Class II · Nov 17, 2020
Latest inspection
May 29, 2025 · VAI

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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
Inspections31Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent Recalls

NumberClassProductDate
D-0149-2021Class IIKollidon CL-M Crospovidone Ph.Eur.Type B, USP/NF, JP, micronized, packaged in 30 kg plastic drums…Nov 17, 2020

Recent FDA Inspections

DateSiteProductClassificationFEI
May 29, 2025East Setauket, NYDrugsVoluntary Action Indicated (VAI)1000521506
Dec 4, 2024Edison, NJFood/CosmeticsNo Action Indicated (NAI)3003165270
Sep 11, 2024Bishop, TXDrugsNo Action Indicated (NAI)3001451837
Jul 22, 2024Geismar, LADrugsVoluntary Action Indicated (VAI)2316568
May 25, 2023Ballerup, DenmarkDrugsVoluntary Action Indicated (VAI)1000474076
Sep 17, 2020Geismar, LAVeterinaryNo Action Indicated (NAI)2316568
Feb 27, 2020Ballerup, DenmarkDrugsVoluntary Action Indicated (VAI)1000474076
Oct 9, 2018Geismar, LAVeterinaryNo Action Indicated (NAI)2316568
Dec 12, 2017Washington, NJVeterinaryNo Action Indicated (NAI)2226532
Nov 17, 2017East Setauket, NYDrugsVoluntary Action Indicated (VAI)1000521506
Jul 14, 2016Geismar, LAVeterinaryNo Action Indicated (NAI)2316568
May 18, 2016Washington, NJDrugsNo Action Indicated (NAI)2226532
Oct 23, 2015Bishop, TXDrugsVoluntary Action Indicated (VAI)3001451837
Jun 19, 2015Gunsan-Si, Korea (The Republic Of)Food/CosmeticsNo Action Indicated (NAI)3009954383
Apr 17, 2015Ballerup, DenmarkDrugsVoluntary Action Indicated (VAI)1000474076
Dec 4, 2014Washington, NJVeterinaryVoluntary Action Indicated (VAI)2226532
Feb 20, 2014Geismar, LADrugsNo Action Indicated (NAI)2316568
Oct 25, 2013Bishop, TXDrugsVoluntary Action Indicated (VAI)3001451837
Aug 23, 2013Brattvag, NorwayFood/CosmeticsNo Action Indicated (NAI)1000287173
May 28, 2013Washington, NJDrugsVoluntary Action Indicated (VAI)2226532

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 1000521506East Setauket, NY3May 29, 2025
FEI 3003165270Edison, NJ2Dec 4, 2024
FEI 3001451837Bishop, TX5Sep 11, 2024
FEI 2316568Geismar, LA5Jul 22, 2024
FEI 1000474076Ballerup, Denmark3May 25, 2023
FEI 2226532Washington, NJ7Dec 12, 2017
FEI 3009954383Gunsan-Si, Korea (The Republic Of)1Jun 19, 2015
FEI 1000287173Brattvag, Norway1Aug 23, 2013
FEI 3008189204Kalundborg, Denmark2Mar 22, 2012
FEI 1000080714Florham Park, NJ1Jan 5, 2011
FEI 3008389780Peekskill, NY1Sep 7, 2010

FDA data resources

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