RecallHawk
Class II Recall

Ziyad cinnamon powder, retail 4.5oz plastic jar with shaker cap UPC 074265007432, 12 retail jars per wholesale case

ZB Importing LLC

Summary

The FDA issued a Class II for Ziyad cinnamon powder, retail 4.5oz plastic jar with shaker cap UPC 074265007432 by ZB Importing LLC. Reason: Elevated levels of lead.

Details

Source

Food Recall

External ID

F-0830-2023

Action Date

2023-05-17

Status

Terminated

Category

food

Product Description

Ziyad cinnamon powder, retail 4.5oz plastic jar with shaker cap UPC 074265007432, 12 retail jars per wholesale case

Lot/Code Info: LOT 21321G2 Best by 01/2024

Quantity Affected: 3,456 units

Reason for Recall

Elevated levels of lead

Distribution

AL, AR, AZ, CA, CT, DE, FL, IA, IL, IN, KS, LA, MA, MD, MI, MN, MO, NC, ND, NE, NM, NV, NY, OH, OK, PA, PR, SC, TN, TX, USVI, UT, VA, VT, WA, WI

Type: Voluntary: Firm initiated

Recall Initiated: 2023-04-25

Company

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

ZB Importing LLC has 8 FDA actions in our database, including 8 recalls.

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

How often does ZB Importing LLC have FDA actions?

ZB Importing LLC has 8 FDA actions in our database, including 8 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0830-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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