FDA recall record

Northern Valley Baking Co The Other Macaroon G'nache P'nache 5.3 oz recall — FDA F-1747-2014

Northern Valley Baking Company did not declare milk or soy on the allergen statement of G'nache P'nache.

Class IIclassification
F-1747-2014official record ID
Apr 16, 2014report date

Recall record at a glance

Official recordF-1747-2014
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmNorthern Valley Baking Co.
Report dateApr 16, 2014
Recall initiation dateFeb 13, 2014
Quantity600 containers
LocationDumont, NJ, United States

Official product description

The Other Macaroon G'nache P'nache 5.3 oz. Manufactured and Distributed by:Northern Valley Baking Co LLC, Dumont, New Jersey USA

Why the product was recalled

Northern Valley Baking Company did not declare milk or soy on the allergen statement of G'nache P'nache.

Distribution information

Nationwide.

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.