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Agropur MSI Ingredients LLC Recall: JayRobb Unflavored Egg White Protein Product is being recalled due to undeclared milk.

United States

TerminatedClass I

Company
Agropur MSI Ingredients LLC
Product
Jay Robb Unflavored Egg White Protein, Net Weight 24 oz (1.5…
Recall date
November 16, 2018
Terminated
April 9, 2019
Source
FDA

Reason for recall

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

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Jay Robb Unflavored Egg White Protein, Net Weight 24 oz (1.5lbs) 680g. Dietary Supplement. UPC 03907-00492. Jay Robb, Inc., Jupiter, FL 33458 03907-00492 1,956 pouches lot 8080-2C3 Best if used by: 03/2020 lot 8056-4C3 Best if used by: 02/2020

Distribution

  • Nationwide

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0717-2019
Event ID
81591
Status
Terminated
Classification
Class I
Company
Agropur MSI Ingredients LLC
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
Quantity
1,956 pouches
Reason
JayRobb Unflavored Egg White Protein Product is being recalled due to undeclared milk.
Recall initiation date
November 16, 2018
Report date
December 12, 2018
Classification date
Not published in this source record
Termination date
April 9, 2019
Distribution pattern
Nationwide
UPC, lot, and code information
UPC 03907-00492; lot 8080-2C3 Best if used by: 03/2020 lot 8056-4C3 Best if used by: 02/2020
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Agropur MSI Ingredients LLC

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.