RecallHawk
Class I Recall

Litehouse item 15533 Ranch dressing packaged in 1.25 oz. plastic cup with seal, 336 cups per case. It is printed on the

Litehouse Inc

Summary

The FDA issued a Class I for Litehouse item 15533 Ranch dressing packaged in 1.25 oz. plastic cup with seal, by Litehouse Inc. Reason: Undeclared anchovies..

Details

Source

Food Recall

External ID

F-0016-2022

Action Date

2021-10-20

Status

Terminated

Category

food

Product Description

Litehouse item 15533 Ranch dressing packaged in 1.25 oz. plastic cup with seal, 336 cups per case. It is printed on the side of a plastic cup as 1231 1.25 OZ 02 83027 15533 RANCH. These cups are un-labeled and not intended for sale as individual cup at retail stores. The master case label is read in parts: "***RANCH DRESSING*** Keep Refrigerated ***15533***336/1.25 OZ UL/RPC RANCH ***Packed By Litehouse Inc. Sandpoint, ID***".

Lot/Code Info: lot 15533 02 011622 15533 = Litehouse Item Code. 02= facility code Lowell Michigan 011622 = best if used by date Jan. 16, 2022

Quantity Affected: 1063 cases (336 cups per case)

Reason for Recall

Undeclared anchovies.

Distribution

distributed in GA and NJ.

Type: Voluntary: Firm initiated

Recall Initiated: 2021-09-20

Company

Litehouse Inc

Sandpoint, ID

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 17 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Litehouse Inc has 2 FDA actions in our database, including 2 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

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 (Litehouse Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Litehouse Inc have FDA actions?

Litehouse Inc has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0016-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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