FDA recall record

Atlantic Fisheries Fresh Mahi Mahi Fillets,10 lb Styrofoam case, labeled in part recall — FDA F-2128-2012

Atlantic Fisheries recalled 580 lbs of Mahi Mahi Fillets due to histamine levels over 50 ppm.

Class IIclassification
F-2128-2012official record ID
Sep 12, 2012report date

Recall record at a glance

Official recordF-2128-2012
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmAtlantic Fisheries
Report dateSep 12, 2012
Recall initiation dateAug 13, 2012
Quantity580 lbs
LocationMiami, FL, United States

Official product description

Fresh Mahi Mahi Fillets,10 lb Styrofoam case, labeled in part: "***Mahi Fillets S/ON Costa Rica Wild****KEEP AT 38 OR BELOW Keep refrigerated***ATLANTIC FISHERIES 8195 NW 67TH ST MIAMI FLORIDA 33166***TEL***FAX 305-594-4301***PACK U.S.A.

Why the product was recalled

Atlantic Fisheries recalled 580 lbs of Mahi Mahi Fillets due to histamine levels over 50 ppm.

Distribution information

Product was distributed to Winn Dixie Distribution Centers in FL, AL, and LA.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.