FDA recall record

Hillside Quickie Too New York Deli Tofu is is tofu sandwich on bread or a bun recall — FDA F-3239-2015

Product contains wheat bun but the ingredients statement does NOT declare wheat and the Contains statement declared Soy only.

Class IIclassification
F-3239-2015official record ID
Sep 30, 2015report date

Recall record at a glance

Official recordF-3239-2015
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmHillside Quickie Too
Report dateSep 30, 2015
Recall initiation dateAug 25, 2015
Quantitydid not provide
LocationTacoma, WA, United States

Official product description

New York Deli Tofu is is tofu sandwich on bread or a bun, enclosed in a clam shell with label

Why the product was recalled

Product contains wheat bun but the ingredients statement does NOT declare wheat and the Contains statement declared Soy only.

Distribution information

distributed in Washington

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: 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.