Distribuidora La Jugosita, Inc. FDA Warning (2017)
Compiled by the Supplement Safety Data Team | Sourced from Official FDA Records on August 17, 2017
Executive Summary
The FDA issued a warning letter to Distribuidora La Jugosita, Inc. on August 17, 2017 citing regulatory violations. The letter was issued by San Juan District Office.
Detailed Analysis
False Claims and Regulatory Violations
The prevention of cross-contamination;
Potential Health Risks
Consumers should be aware of potential risks associated with products from Distribuidora La Jugosita, Inc..
Regulatory Context
The protection of food, food packaging material, and food contact surfaces fromadulteration;
The condition and cleanliness of food contact surfaces;
The document “Record de Control de Sanitización Diaria” [in English: Daily Sanitation Control Record] does not provide for documenting the exact time when the pre-operational and operational sanitation monitoring steps are conducted.
Key Entities Identified
Frequently Asked Questions
- What did the FDA find wrong with Distribuidora La Jugosita, Inc.?
- The FDA issued a warning letter citing regulatory violations related to their products or manufacturing practices.
- Are Distribuidora La Jugosita, Inc. products safe to use?
- Based on the FDA's findings, consumers should exercise caution. The company was found to have regulatory issues that may affect product safety.
- What should I do if I've used Distribuidora La Jugosita, Inc. products?
- If you have used products from Distribuidora La Jugosita, Inc. and experience any adverse effects, contact your healthcare provider immediately. You can also report adverse events to the FDA's MedWatch program.
Source Document
This report is based on an official FDA warning letter. The original document is a public record.
View Original FDA Warning Letter