FDA recall record

Ballester Hermanos Product in cans of 4 1/4 oz and 8 1/4 oz net weight recall — FDA F-0003-2017

Product label states name and ingredients as Octopus and real content is Squid.

Class IIclassification
F-0003-2017official record ID
Oct 12, 2016report date

Recall record at a glance

Official recordF-0003-2017
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmBallester Hermanos, Inc.
Report dateOct 12, 2016
Recall initiation dateMay 12, 2016
Quantity166 CASES
LocationCatano, PR, United States

Official product description

Product in cans of 4 1/4 oz and 8 1/4 oz net weight. Label reading in part as: "Coloso***PULPO EN ACEITE PICANTE***OCTOPUS IN HOT OIL***NET WEIGHT ***Fabricado en Espa¿a (Manufactured in Spain)***Packed by: POYO PONTEVEDRA SPAIN***PACKED FOR COLOSO FOODS, INC.*** MERCADO CENTRAL PUERTO NUEVO SAN JUAN PUERTO RICO".

Why the product was recalled

Product label states name and ingredients as Octopus and real content is Squid.

Distribution information

Puerto Rico only.

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.