Prime Food Processing LLC. food recall: Prime Food Processing Dried Croaker Fish
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Ongoing
- Event ID
- 98390
- Recall initiated
- Feb 3, 2026
- Classified by FDA
- Feb 20, 2026
- Posted in Enforcement Report
- Mar 4, 2026
- Recalling firm
- Prime Food Processing LLC.
- Firm location
- Brooklyn, NY, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Products in this event
- 1
What to do
Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.
Reason for recall
Uneviscerated Fish
What the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on Feb 3, 2026. FDA classified it 17 days later, on Feb 20, 2026. Distribution reported by FDA: AZ, CA, FL, GA, HI, ID, MA, MD, MO, NJ, NV, NY, OH, OK, PA, VA, WA, WI Prime Food Processing LLC. has 4 recalls in our records.
Recalled products (1)
H-0519-2026 Class I Ongoing
Prime Food Processing Dried Croaker Fish; NET WT: 8oz (227g); Ingredients: Croaker Fish, Salt; CONTAINS: FISH (CROAKER FISH); DISTRIBUTED BY: PFP LLC, Brooklyn, NY, 11211, USA; Product must be thoroughly cleaned and cooked before consumption.; PRODUCT OF VIETNAM; UPC: 6 946976 818000
Codes / lots: Item #AF1410 Expiration: 12-28-27 UPC Codes: #946976818000
Quantity: 79 cases
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
- Official notice
- FDA Enforcement Report, event 98390
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.