FDA recall record

AMS Health Sciences Saba Shark Cartilage Complex Dietary Supplement, 500 mg, 60 recall — FDA F-0462-2015

The product is being recalled due to the potential presence of Salmonella.

Class Iclassification
F-0462-2015official record ID
Nov 12, 2014report date

Recall record at a glance

Official recordF-0462-2015
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmAMS Health Sciences
Report dateNov 12, 2014
Recall initiation dateOct 15, 2014
Quantity2,014 bottles
LocationOklahoma City, OK, United States

Official product description

Saba Shark Cartilage Complex Dietary Supplement, 500 mg, 60 Capsules, Distributed by Saba 711 NE 39th Street, Oklahoma City, OK 73105

Why the product was recalled

The product is being recalled due to the potential presence of Salmonella.

Distribution information

Nationwide throughout the US and in Canada

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement 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.

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