FDA recall record

Ricker Hill Farms recall — FDA F-0004-2018

Product contains patulin at levels higher than the FDA established limit of 50ppb

Class IIclassification
F-0004-2018official record ID
Oct 11, 2017report date

Recall record at a glance

Official recordF-0004-2018
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmRicker Hill Farms
Report dateOct 11, 2017
Recall initiation dateSep 28, 2017
Quantity230 cases (9/cs Half-Gallon) and 62 cases (24/cs12 oz bottles
LocationTurner, ME, United States

Official product description

(1) Ricker Hill Orchards Apple Cider packaged in plastic Half Gallon UV Treated (64 fl. oz.) Jugs UPC 7461380009 (2) Northland Apples Sweet Maine Cider, 12 oz plastic bottle UPC 7461360009

Why the product was recalled

Product contains patulin at levels higher than the FDA established limit of 50ppb

Distribution information

Maine

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.