FDA recall record

Interpac Technologies think Thin Protein & Fiber Oatmeal, Madagascar Vanilla recall — FDA F-3075-2015

A small number of think Thin Madagascar Vanilla with Almonds & Pecans oatmeal have the correct lid but have the incorrect Honey Peanut Butter label around…

Class IIclassification
F-3075-2015official record ID
Sep 9, 2015report date

Recall record at a glance

Official recordF-3075-2015
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmInterpac Technologies
Report dateSep 9, 2015
Recall initiation dateAug 14, 2015
Quantity27, 408 individual cups, 2284 trays of 12 x 1.76 oz. cups.
LocationWoodland, CA, United States

Official product description

think Thin Protein & Fiber Oatmeal, Madagascar Vanilla, Almonds, Pecans; 10 g Protein, 5 g Fiber, 190 calories; Net wt 1.76 oz. (50g); (Nuts are visible in product when lid is opened. Tray - 12 x 1.76 oz cups UPC 753656711881: Individual cup UPC 753656 711874 Ingredients: Whole rolled oats, steel cut oats, almonds, pecans, red quinoa,saved caned syrup, isolated soy protein, crunchy root fiver, natural flavorings, almonds, pecans, sea salt, ground Madagascar vanilla. GMO free Manufactured in a facility that also processes peanuts, tree nuts, wheat, egg and milk. Distributed by Think Thin, LLC, Los Angeles, CA. Product of USA.

Why the product was recalled

A small number of think Thin Madagascar Vanilla with Almonds & Pecans oatmeal have the correct lid but have the incorrect Honey Peanut Butter label around the cup. The nuts are obvious once the lid is removed.

Distribution information

GA, CO, CA, NJ, SC, IL, WI, FL, IA, TN, OR, PA, ID, TX,, NY, NH.

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.