RecallHawk
Class I Recall

SALUTE SEASONINGS; Ground All Spice; Net Wt 16oz; Unistel Industries 650 Blossom Road Rochester, NY 14610; UPC: 7 69203

Unistel Industries Inc.

Summary

The FDA issued a Class I for SALUTE SEASONINGS; Ground All Spice; Net Wt 16oz; Unistel Industries 650 Blossom by Unistel Industries Inc.. Reason: Product may be contaminated with Salmonella..

Details

Source

Food Recall

External ID

H-0666-2026

Action Date

2026-04-29

Status

Ongoing

Category

food

Product Description

SALUTE SEASONINGS; Ground All Spice; Net Wt 16oz; Unistel Industries 650 Blossom Road Rochester, NY 14610; UPC: 7 69203 01617 0

Lot/Code Info: Lot: A6040, A6054, A6068

Quantity Affected: 330 units

Reason for Recall

Product may be contaminated with Salmonella.

Distribution

CA, HI, WA

Type: Voluntary: Firm initiated

Recall Initiated: 2026-03-24

Company

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 12 food recalls issued in the same week, part of 204 food-related FDA actions this month.

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

How often does Unistel Industries Inc. have FDA actions?

This is the only FDA action we have on record for Unistel Industries Inc. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0666-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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