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Lower risk Food recall · FDA · Published November 9, 2020

Mayer Brothers Premium Apple Cider Recall: Mixing of Pasteurized and Raw Cider

Mayer Brothers recalls 64 fl oz and 128 fl oz apple cider due to processing error mixing pasteurized and raw cider. Consumers should check UPC codes and lot numbers for affected products.

🇺🇸 FDA recall #F-0151-2021FoodMayer Brothers ›
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Contact the company

Recalling firmMayer Brothers Apple Products, Inc.3300 Transit Rd · West Seneca, NY 14224-2525
✎ GovInfoNow plain-language explainer

Mayer Brothers is recalling two types of apple cider products because a processing error mixed pasteurized and raw cider into the final product. This could lead to unsafe consumption of the cider. Read more at govinfonow.com/recall/15029-mayer-brothers-premium-apple-cider-recall-mixing-of-pasteurized-and.

Source Summary by GovInfoNow · govinfonow.com/recall/15029-mayer-brothers-premium-apple-cider-recall-mixing-of-pasteurized-and · Updated October 4, 2026 · FDA enforcement record: FDA #F-0151-2021

Cite this page

“Mayer Brothers Premium Apple Cider Recall: Mixing of Pasteurized and Raw Cider.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/15029-mayer-brothers-premium-apple-cider-recall-mixing-of-pasteurized-and. Based on FDA recall #F-0151-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0151-2021%22&limit=1).

The FDA announced on Nov. 9, 2020, that Mayer Brothers Apple Products, Inc. voluntarily recalled apple cider due to a processing error mixing pasteurized and raw cider. The recall affects products distributed by Foodhold USA LLC, Aldi, Inc., and others.

How to tell if you have it

  • Giant brand Premium Apple Cider 64 fl. oz., UPCs 00022198008095, 00688267033100, 00884853622707
  • Nature's Nectar 100% Fresh Apple Cider 128 fl. oz., UPC 099100217933, PRO 110720 BB 122220
  • Open Acres Honeycrisp Apple Cider 128 fl. oz., Lot/Unit Numbers PRO 110720, Best by 01/26/21, UPC 884853622707
  • Mayer Bros. Apple Cider 128 fl. oz., Lot/Unit Numbers PRO 110720, product date 2/05/21, UPC 022198008095

The hazard

The recall stems from a processing error resulting in the mixing of pasteurized and raw cider into the final product. The FDA classified this as a Class II recall.

Context

GovInfoNow's records show other recent recalls of similar products include Weis Pasteurized Apple Cider Recall (2026-08-06), Mehadrin Chocolate Leben Recall (2026-08-10), and Joy Sweet Lassi 16oz Recall (2026-04-23).

How to tell if you have this one

Check for the following: 64 fl oz (1.89L) Giant Premium Apple Cider with UPC 688267033100 or lot numbers PRO 110720 BB020521/BB020621; 128 fl oz Nature's Nectar 100% Fresh Apple Cider with UPC 099100217933 or lot numbers PRO 110720; and Open Acres Honeycrisp Apple Cider.

  • Brand
    Mayer Brothers
  • Product
    1. Giant brand " Premium Apple Cider*** 64 fl. oz. (Half Gal) 1.89L***Distributed by Foodhold USA LLC, Landover, MD
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Labels

    Look for the product name, size, and UPC code on the label to determine if it matches the recalled items.

  2. Contact Manufacturer

    If you have the recalled product, contact Mayer Brothers Apple Products, Inc. for further instructions.

Where it went and when

Where it was distributed

Distributed in 3 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: yesMINew York: not listedNYRhode Island: not listedRIMassachusetts: yesMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: yesMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “MD, MA, MI” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Maryland, Massachusetts, Michigan.

Recall timeline

FDA terminated this recall 49 days after the firm started it.

1. Firm started the recall: Nov 9, 202012. Published in FDA’s Enforcement Report: Nov 25, 202023. FDA classified it Class II: Dec 7, 202034. FDA terminated the recall: Dec 28, 202042020
  1. Firm started the recall
  2. Published in FDA’s Enforcement Report
  3. FDA classified it Class II
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-0151-2021 (November 9, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0151-2021 to see it in context.
  • Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA