Dole Baby Spinach Recall Issued Due to Salmonella Poisoning Risk

Certain Dole baby spinach products may carry a risk of salmonella food poisoning, resulting in a nationwide recall.

The FDA announced the Dole baby spinach recall on August 9, after random sample testing conducted by the Department of Agriculture in Michigan discovered the presence of salmonella bacteria. However, no illnesses or food poisoning outbreak has yet been linked to the products.

Did You Know?

Ticketmaster Data Breach Impacts Millions of Customers

A massive Ticketmaster data breach exposed the names, addresses, phone numbers, credit card numbers and other personal information of more than 560 million customers, which have now been released on the dark web. Lawsuits are being pursued to obtain financial compensation.

Learn More

The recalled baby spinach products were packaged in clear 6-ounce bags with lot code W20308A and UPC code 0-71430-00964-2 and 10-ounce bags of Dole baby spinach clamshells packages with lot code W203010 and UPC code 0-71430-00016-8.

According to the recall notice, the impacted lots have a “Use-by” date of August 5, 2019 and should no longer be available on store shelves. However, officials are encouraging customers to check for the recalled baby spinach products in their homes and discard any remaining recalled items.

The spinach was distributed to various grocery stores in Illinois, Indiana, Kentucky, Michigan, New Jersey, New York, Ohio, Tennessee, Virginia and Wisconsin. A list of affected grocers and retailers was not been released.

Retailers and customers with additional questions or concerns regarding the recall are being asked to contact Dole Customer Center at 1-800-356-3111.

Salmonella food poisoning can cause mild to severe health consequences depending upon the individual. The bacteria may cause a healthy person to experience fever, diarrhea, nausea, vomiting, and abdominal pain whereas the young or elderly with weakened immune systems may face more severe consequences, including fatal infections.

Among pregnant women, salmonella poisoning may cause still births and miscarriages. Occasionally, salmonella infections may travel through the bloodstream and produce illnesses such as arterial infections, endocarditis and arthritis, which can cause severe to potentially life threatening health consequences.

The U.S. Centers for Disease Control and Prevention (CDC) estimates salmonella causes approximately 1.2 million illnesses annually. Of those cases, an average of 1,200 hospitalizations and 450 deaths occur every year from salmonella infections.

0 Comments

Share Your Comments

I authorize the above comments be posted on this page*

Want your comments reviewed by a lawyer?

To have an attorney review your comments and contact you about a potential case, provide your contact information below. This will not be published.

NOTE: Providing information for review by an attorney does not form an attorney-client relationship.

This field is for validation purposes and should be left unchanged.

More Top Stories

Ozempic MDL Court To Evaluate Need for Gastroparesis Diagnostic Testing in GLP-1 Lawsuits
Ozempic MDL Court To Evaluate Need for Gastroparesis Diagnostic Testing in GLP-1 Lawsuits (Posted yesterday)

A federal judge has agreed to divide lawsuits over gastroparesis injuries linked to drugs like Ozempic and Mounjaro into multiple phases, examining how the condition is diagnosed and whether plaintiffs' claims are preempted by federal laws.

Adult Woman Files Similac Lawsuit Over NEC Injuries Experienced as a Newborn
Adult Woman Files Similac Lawsuit Over NEC Injuries Experienced as a Newborn (Posted 2 days ago)

Lawsuit alleges that Abbott Laboratories failed to provide families and the medical community with adequate warnings about the risks associated with it’s cow’s milk-based Similac formula, which a now adult woman indicates has left her with life-long NEC injuries.

Amended Lawsuit Over BioZorb Implant Side Effects Outlines Problems Caused By Tissue Marker Design Defects
Amended Lawsuit Over BioZorb Implant Side Effects Outlines Problems Caused By Tissue Marker Design Defects (Posted 3 days ago)

Six breast cancer patients have asked a federal judge for permission to amend a complaint filed in March 2024, which describes problems linked to the device and painful side effects experienced when the tissue marker migrated out of position or shattered inside their bodies.