CLASS I ONGOING Food recall · Reported 1 Jul 2026 · FDA Enforcement Report

Dried Herring Fish recalled by Prime Food Processing

Prime Food Processing is recalling Dried Herring Fish, distributed in 19 states. The recall was initiated on 2 Jun 2026 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot Code: 26020. Expiration: 06.12.28 UPC Codes: 6946976817911
Quantity recalled69 cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-1080-2026
FDA event ID
99147
Recalling firm
Prime Food Processing, Brooklyn, NY
Classification
Class I
Status
Ongoing
Recall initiated
2 Jun 2026
FDA classified
22 Jun 2026
Reported
1 Jul 2026
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Botulism
Product category
Fish

Timeline

2 Jun 2026Recall initiated by company
22 Jun 2026Classified by FDA+20 days
1 Jul 2026Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Improperly eviscerated which may result in Clostridium botulinum contamination

Product as listed by the FDA

Dried Herring Fish 7 oz.

Where it was distributed

AZ, CA, FL, HI, IL, KS, LA, MD, MO, NC, NH, NV, NY, OK, OR, PA, TX, UT, WA

ArizonaCaliforniaFloridaHawaiiIllinoisKansasLouisianaMarylandMissouriNorth CarolinaNew HampshireNevadaNew YorkOklahomaOregonPennsylvaniaTexasUtahWashington

Questions about this recall

Why was it recalled?

Improperly eviscerated which may result in Clostridium botulinum contamination

Which lots are affected?

Lot Code: 26020. Expiration: 06.12.28 UPC Codes: 6946976817911

Where was it sold?

AZ, CA, FL, HI, IL, KS, LA, MD, MO, NC, NH, NV, NY, OK, OR, PA, TX, UT, WA

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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