FDA recall record

Agropur MSI Ingredients Jay Robb Unflavored Egg White Protein, Net Weight 24 oz recall — FDA F-0717-2019

JayRobb Unflavored Egg White Protein Product is being recalled due to undeclared milk.

Class Iclassification
F-0717-2019official record ID
Dec 12, 2018report date

Recall record at a glance

Official recordF-0717-2019
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmAgropur MSI Ingredients LLC
Report dateDec 12, 2018
Recall initiation dateNov 16, 2018
Quantity1,956 pouches
LocationLa Crosse, WI, United States

Official product description

Jay Robb Unflavored Egg White Protein, Net Weight 24 oz (1.5lbs) 680g. Dietary Supplement. UPC 03907-00492. Jay Robb, Inc., Jupiter, FL 33458

Why the product was recalled

JayRobb Unflavored Egg White Protein Product is being recalled due to undeclared milk.

Distribution information

Nationwide

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.