Myers Cider Mill 1 Gallon Apple Cider Recall: Process Deviation Risk
Myers Cider Mill recalls 1-gallon apple cider produced between September 2016 and October 2016 due to a process deviation. Consumers should check UPC 085591001281 for affected products.
Lower-risk recall
Myers Cider Mill LLC, of Monroeville, Ohio has issued a voluntary recall of apple cider due to a process deviation.
Contact the company
What happened, in plain English
Myers Cider Mill is recalling 1-gallon apple cider produced between September 1, 2016 and October 15, 2016 because of a process deviation. This recall affects consumers who purchased the product with the specified UPC code and press dates. Read more at govinfonow.com/recall/23002-myers-cider-mill-1-gallon-apple-cider-recall-process-deviation.
Source Summary by GovInfoNow · govinfonow.com/recall/23002-myers-cider-mill-1-gallon-apple-cider-recall-process-deviation · Updated October 9, 2026 · FDA enforcement record: FDA #F-1954-2017
Cite this page
“Myers Cider Mill 1 Gallon Apple Cider Recall: Process Deviation Risk.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23002-myers-cider-mill-1-gallon-apple-cider-recall-process-deviation. Based on FDA recall #F-1954-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1954-2017%22&limit=1).
Why it’s dangerous
The recall is due to a process deviation during production, which could potentially affect product quality but does not indicate a safety hazard that causes injury or illness.
Who’s affected
Consumers who purchased Myers Cider Mill 1-gallon apple cider with UPC 085591001281 between September 1, 2016 and October 15, 2016 are affected. Those who have the product are most at risk.
How to tell if you have this one
Check for the UPC code 085591001281 on the product label. The product was manufactured between September 1, 2016 and October 15, 2016.
- Brand
Myers Cider Mill- Category
Food
What to do — step by step
Check Product Label
Look for the UPC code 085591001281 and press dates between September 1, 2016 and October 15, 2016.
Where it went and when
Where it was distributed
Distributed in Ohio.
FDA distribution: “Product was only sold in OH” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Ohio.
Recall timeline
FDA terminated this recall 3.2 years after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
Is this cider safe to drink?
The recall is due to a process deviation, not a safety hazard. The product is safe to drink but should be discarded as part of the recall.
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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-1954-2017 (October 19, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1954-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 9, 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.