Home » Martinelli’s Recalls 170,000 Apple Juice Bottles Due to Potential Fungal Contamination

Martinelli’s Recalls 170,000 Apple Juice Bottles Due to Potential Fungal Contamination

by TodayUS
Martinelli's recalls 170,000 apple juice bottles due to potential fungal

Martinelli’s Apple Juice Recall: Contamination Risk Identified

Overview of the Recall

In a recent announcement, S. Martinelli & Co. has initiated a recall for over 170,000 bottles of its apple juice, citing potential contamination with patulin, a harmful mycotoxin produced by certain fungi. The recall impacts round glass 10-ounce bottles that feature white metal screw-top lids.

Details of Affected Products

The recalled apple juice bottles were distributed across 28 states, spanning from Alabama to Wisconsin, according to the FDA recall notice. The bottles bear a “best by” date of December 5, 2026, and feature the UPC code 0 41244 04102 2.

Classification and Health Risks

This recall has been classified as Class II by the FDA. This classification indicates that while the product may cause temporary or reversible health issues, the likelihood of serious consequences is minimal. Health effects associated with patulin may include symptoms such as nausea, vomiting, and diarrhea, as highlighted in research published in the journal Toxicon.

Distribution States

The recall includes the following states:

  • Alabama
  • Arkansas
  • Arizona
  • California
  • Connecticut
  • Delaware
  • Florida
  • Georgia
  • Iowa
  • Illinois
  • Indiana
  • Kansas
  • Kentucky
  • Louisiana
  • Michigan
  • Missouri
  • Mississippi
  • North Carolina
  • New Hampshire
  • New Jersey
  • New York
  • Ohio
  • Pennsylvania
  • South Carolina
  • Texas
  • Utah
  • Virginia
  • Wisconsin

For those who may have purchased these products, it is advised to dispose of the bottles and refrain from consuming the juice until further information is disclosed by Martinelli’s. This precaution is critical to ensure consumer safety.

For further updates and inquiries, refer to the FDA’s official recall notice.

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