Sunnyside Orchards Apple Cider Recall: Underprocessed Cider Risk
Sunnyside Orchards recalls half-gallon and gallon apple cider in plastic containers due to potential underprocessing. Keep refrigerated; check for colored caps (dark blur, light blue, red, orange).
Lower-risk recall
Apple Cider may be under processed.
Contact the company
What happened, in plain English
Sunnyside Orchards is recalling half-gallon and gallon apple cider containers because the cider may not be processed enough. This could lead to safety issues if the cider is consumed without proper processing. Read more at govinfonow.com/recall/18405-sunnyside-orchards-apple-cider-recall-underprocessed-cider-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/18405-sunnyside-orchards-apple-cider-recall-underprocessed-cider-risk · Updated October 6, 2026 · FDA enforcement record: FDA #F-0627-2019
Cite this page
“Sunnyside Orchards Apple Cider Recall: Underprocessed Cider Risk.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/18405-sunnyside-orchards-apple-cider-recall-underprocessed-cider-risk. Based on FDA recall #F-0627-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0627-2019%22&limit=1).
Why it’s dangerous
The cider may be underprocessed, meaning it could have unsafe bacteria levels if not handled correctly. This risk is higher if the cider is not kept refrigerated as instructed.
Who’s affected
Owners of Sunnyside Orchards apple cider in half-gallon or gallon plastic containers with colored caps (dark blur, light blue, red, or orange) are affected. Those who consume the cider without proper refrigeration may be at risk.
How to tell if you have this one
Check for Sunnyside Orchards apple cider in half-gallon or gallon plastic containers. Look for colored caps: dark blur, light blue, red, or orange.
- Brand
Sunnyside Orchards- Category
Food
What to do — step by step
Check Product Details
Identify if your cider has colored caps (dark blur, light blue, red, or orange) and is in half-gallon or gallon plastic containers.
Where it went and when
Where it was distributed
Distributed in Minnesota.
FDA distribution: “MN” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Minnesota.
Recall timeline
FDA terminated this recall 16 months 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.
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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-0627-2019 (October 12, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0627-2019 to see it in context.
- Plain-language summary written by qwen3:4b on October 6, 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.