Food Recall Check
Class II · Moderate risk Terminated Initiated Nov 9, 2020 (6 years ago)

1. Giant brand " Premium Apple Cider*** recall

Recalled by Mayer Brothers Apple Products, Inc. · West Seneca, NY, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Processing error resulting in mixing of pasteurized and raw cider into final product.

These are failures of the safety steps that keep food safe - cooking, pasteurising, keeping cold, sealing - even when no contaminant has yet been found. All processing & sanitation problems recalls.

What was recalled

1. Giant brand " Premium Apple Cider*** 64 fl. oz. (Half Gal) 1.89L***Distributed by Foodhold USA LLC, Landover, MD 20785" 2. "Nature's Nectar 100% Fresh Apple Cider***128 fl. oz.***Distributed by Aldi, Inc. Batavia, IL 60510" 3. Open Acres Honeycrisp Apple Cider, 128 fl. oz 4. Mayer Bros. Apple Cider, 128 fl. oz.

Quantity: 27,189 half gallons and 8,448 gallons (total - 22042.5 gallons)

Food: Fresh fruit

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.

1.Giant Premium Apple Cider 64 fl oz UPC: 688267033100 Codes: PRO 110720 BB020521 and PRO 110820 BB020621 2. UPC: 099100217933 PRO 110720 BB 122220 3.Lot/Unit Numbers: PRO 110720 Best by:01/26/21 UPC Codes: 884853622707 4. Lot/Unit Numbers: PRO 110720 product: 2/05/21 UPC Codes: 022198008095

Where it was sold

Massachusetts Maryland Michigan

FDA's distribution note: MD, MA, 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
Mayer Brothers Apple Products, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Nov 9, 2020
In FDA report of
Nov 25, 2020
Terminated
Dec 28, 2020
FDA recall number
F-0151-2021 · event 86732
Official record
FDA enforcement report search

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