RecallHawk
Class II Recall

Food grade Anhydrous 94-97% Calcium Chloride Pellets, 50 lb. plastic bag

Occidental Chemical Corporation

Summary

The FDA issued a Class II for Food grade Anhydrous 94-97% Calcium Chloride Pellets, 50 lb. plastic bag by Occidental Chemical Corporation. Reason: product may be contaminated with fragments of blue high density polyethylene (HDPE).

Details

Source

Food Recall

External ID

F-0088-2022

Action Date

2021-11-03

Status

Terminated

Category

food

Product Description

Food grade Anhydrous 94-97% Calcium Chloride Pellets, 50 lb. plastic bag

Lot/Code Info: Batches 364JD284A, 364JD284B, and 364JD284C

Quantity Affected: 11,275 bags

Reason for Recall

product may be contaminated with fragments of blue high density polyethylene (HDPE)

Distribution

Distributors in KY, WI, PA, IL, LA, and CANADA

Type: Voluntary: Firm initiated

Recall Initiated: 2021-10-06

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 57 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 (Occidental Chemical Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Occidental Chemical Corporation have FDA actions?

This is the only FDA action we have on record for Occidental Chemical Corporation in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0088-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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