FDA recall record

Superior Foods Archer Farms Corn & Black Bean Quinoa Blend with pineapple & recall — FDA F-2085-2016

Product contains undeclared wheat

Class IIclassification
F-2085-2016official record ID
Sep 14, 2016report date

Recall record at a glance

Official recordF-2085-2016
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmSuperior Foods
Report dateSep 14, 2016
Recall initiation dateAug 11, 2016
Quantity2021 cases
LocationWatsonville, CA, United States

Official product description

Archer Farms Corn & Black Bean Quinoa Blend with pineapple & red pepper packaged in a flexible plastic bag

Why the product was recalled

Product contains undeclared wheat

Distribution information

OH, CA, IA, FL, TX, MD, MA

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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

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.