George J Howe Company, Inc.

FDA Regulatory Profile

George J Howe Company, Inc. has 6 FDA recalls (6 Class I), 13 inspections, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "George J Howe Company, Inc." and its spelling variants "George J Howe Company", "George J Howe".

Latest recall
H-1119-2026 · Class I · Apr 29, 2026
Latest inspection
Apr 8, 2025 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls6 (6 Class I)Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections13Nov 13, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

George J Howe Company, Inc.'s FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

George J Howe Company, Inc.: FDA inspections per year 2017: 1 inspections120172018: 1 inspections120182019: 0 inspections020192020: 1 inspections120202021: 0 inspections020212022: 0 inspections020222023: 0 inspections020232024: 1 inspections120242025: 1 inspections120252026: 0 inspections02026
YearInspectionsOAIWarning lettersRecall recordsClass I
202600066
202510000
202410000
202300000
202200000
202100000
202010000
201900000
201810000
201710000

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.

Recent recalls

6 recall records on Apr 29, 2026.

NumberClassProductDate
H-1119-2026Class I6/11oz No Salt Sunflower SeedsApr 29, 2026
H-1120-2026Class I8/9.5oz Tub Nut - Sunflower SeedApr 29, 2026
H-1118-2026Class I6/11oz Sunflower Seeds SaltedApr 29, 2026
H-1122-2026Class I5# Sunflower Seeds C/NSApr 29, 2026
H-1121-2026Class I5# Sunflower Seeds C/SApr 29, 2026
H-1123-2026Class I25# Sunflower Seeds C/SApr 29, 2026

Recent FDA inspections

13 inspections from Feb 6, 2009 to Apr 8, 2025.

DateSiteProductClassificationFEI
Apr 8, 2025Beaver, PAFood/CosmeticsNo Action Indicated (NAI)3020800865
Jun 7, 2024Grove City, PAFood/CosmeticsNo Action Indicated (NAI)1317926
Jan 30, 2020Grove City, PAFood/CosmeticsNo Action Indicated (NAI)1317926
Jan 9, 2018Grove City, PAFood/CosmeticsNo Action Indicated (NAI)1317926
Mar 8, 2017Grove City, PAFood/CosmeticsNo Action Indicated (NAI)1317926
Jan 3, 2014Grove City, PAFood/CosmeticsVoluntary Action Indicated (VAI)1317926
Sep 30, 2013Grove City, PAFood/CosmeticsNo Action Indicated (NAI)1317926
Dec 20, 2012Grove City, PAFood/CosmeticsVoluntary Action Indicated (VAI)1317926
Aug 4, 2011Grove City, PAFood/CosmeticsNo Action Indicated (NAI)1317926
Mar 9, 2011Grove City, PAFood/CosmeticsNo Action Indicated (NAI)1317926
Apr 15, 2009Grove City, PAFood/CosmeticsNo Action Indicated (NAI)1317926
Apr 1, 2009Grove City, PAFood/CosmeticsNo Action Indicated (NAI)1317926
Feb 6, 2009Grove City, PAFood/CosmeticsNo Action Indicated (NAI)1317926
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

2 inspected sites, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3020800865Beaver, PA1Apr 8, 2025
FEI 1317926Grove City, PA12Jun 7, 2024

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