Martina brand Fresh Whole Mangoes
Reason Product may be contaminated with Salmonella
Eden Organic Apple Juice in 32floz recall
Recalled by Eden Foods, Inc · Clinton, MI, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
culling not performed to remove rotted apples, excessive levels of patulin found in 1 lot
Some of these cause harm only with repeated exposure (lead in spices, for example), others act within hours (histamine poisoning from spoiled fish). All chemical contamination recalls.
What was recalled
Eden Organic Apple Juice in 32floz., 64floz., and 1.82L sizes, all sizes in glass bottle. Glass bottles packed 12, 32floz. bottles per wholesale case and 6, 64floz. / 1.82L bottles per wholesale case. 32floz. UPC code: 0 0024182 00067 2 32floz. GTIN case code: 1 0024182 00067 9 64floz. UPC code: 0 0024182 00064 1 64floz. GTIN case code: 1 0024182 00064 8 1.82 Liter UPC code: 0 0024182 00364 2 1.82 Liter GTIN case code: 1 0024182 00364 9
Quantity: 1,070.2314 cases
Food: Fresh fruit Juice & beverages
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot 1057 Best By 2024FE26 Lot 2042 Best By 2025FE11
Where it was sold
Nationwide.
California Illinois Michigan Minnesota New York Ohio Oklahoma Oregon Pennsylvania Texas Virginia
FDA's distribution note: Wholesale: CA, IL, MI, MN, NY, OH, OK, OR, PA, TX, VA. CANADA CHILE JAPAN SIGNAPORE ecommerce: US Nationwide CANADA Recalling firm's retail store front Clinton, MI
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Eden Foods, Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Aug 19, 2022
- In FDA report of
- Oct 19, 2022
- Terminated
- May 11, 2023
- FDA recall number
- F-0033-2023 · event 90814
- Official record
- FDA enforcement report search
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