FDA recall record

N.A.C. Foods Mi Pepito Camaron Molido Ground Shrimp, Net wt recall — FDA F-1452-2015

Mi Pepto Camaron Molido (Ground Shrimp) contains unallowed dyes: Carmoisine (E122 - acid red 14), Ponceau 4R (E124 acid red 18) and undeclared sulfites.

Class IIclassification
F-1452-2015official record ID
Mar 25, 2015report date

Recall record at a glance

Official recordF-1452-2015
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmN.A.C. Foods
Report dateMar 25, 2015
Recall initiation dateFeb 9, 2015
Quantity42.2 lbs.
LocationPalisades Park, NJ, United States

Official product description

Mi Pepito Camaron Molido Ground Shrimp, Net wt. .75 oz (16 gr), Packaged in a plastic bag, Packed & Distributed by: N.A.C. Corp., Palisades Park, NJ, UPC 707425900051

Why the product was recalled

Mi Pepto Camaron Molido (Ground Shrimp) contains unallowed dyes: Carmoisine (E122 - acid red 14), Ponceau 4R (E124 acid red 18) and undeclared sulfites.

Distribution information

NJ and NY

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: E-Mail.

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.

Related recall records

Other records from the same recalling company are shown first when available.