RecallHawk
Class II Recall

Caramel Butter Pecan Cup 14 fl oz. cup (8 per case) Paper cup with paper lid Brand: Eclipse Foods UPC: 810049270490 Fro

ECLIPSE FOODS CO

Summary

The FDA issued a Class II for Caramel Butter Pecan Cup 14 fl oz. cup (8 per case) Paper cup with paper lid Br by ECLIPSE FOODS CO. Reason: Potential ink pen pieces; foreign object..

Details

Source

Food Recall

External ID

F-1381-2023

Action Date

2023-08-16

Status

Terminated

Category

food

Product Description

Caramel Butter Pecan Cup 14 fl oz. cup (8 per case) Paper cup with paper lid Brand: Eclipse Foods UPC: 810049270490 Frozen

Lot/Code Info: Lot #: MC00923041, Best By: 2/10/2024

Quantity Affected: N/A

Reason for Recall

Potential ink pen pieces; foreign object.

Distribution

NC, SC, VA, MD, DC, DE, IL

Type: Voluntary: Firm initiated

Recall Initiated: 2023-06-30

Company

ECLIPSE FOODS CO

Berkeley, CA

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 102 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (ECLIPSE FOODS CO) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does ECLIPSE FOODS CO have FDA actions?

This is the only FDA action we have on record for ECLIPSE FOODS CO in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1381-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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