McCormick Perfect Pinch Italian Seasoning 1.31 oz. Plastic Bottles, 36 packages per case; 2.25 oz. Plastic bottles, 6
Summary
The FDA issued a Class I for McCormick Perfect Pinch Italian Seasoning 1.31 oz. Plastic Bottles, 36 package by McCormick & Company - MSS - HQ. Reason: Product may be contaminated with Salmonella..
Details
Source
Food Recall
External ID
F-0898-2021
Action Date
2021-08-18
Status
Terminated
Category
food
Product Description
McCormick Perfect Pinch Italian Seasoning 1.31 oz. Plastic Bottles, 36 packages per case; 2.25 oz. Plastic bottles, 6 packages per case
Lot/Code Info: [1.31 oz] UPC NUMBER: 052100049731 MCCORMICK ITEM NUMBER: 901582629 BEST BY MAY 26 24 K, BEST BY MAY 27 24 K, BEST BY JUN 04 24 K, BEST BY JUN 05 24 K; [2.25 oz] UPC NUMBER: 052100038254 MCCORMICK ITEM NUMBER: 901455463 BEST BY JUN 30 24 H, BEST BY JUL 01 24 H
Quantity Affected: 4909 Cases and 760 Cases
Reason for Recall
Product may be contaminated with Salmonella.
Distribution
The recalled product was distributed to the following states : OR,IL,MD,VA,LA,PA,NJ,TX,AR,GA,CA,MA,MI,NH,AR,WI and Canada
Type: Voluntary: Firm initiated
Recall Initiated: 2021-07-26
Company
Hunt Valley, MD
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 56 food recalls issued in the same week, part of 204 food-related FDA actions this month.
McCormick & Company - MSS - HQ has 3 FDA actions in our database, including 3 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 (McCormick & Company - MSS - HQ) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does McCormick & Company - MSS - HQ have FDA actions?
McCormick & Company - MSS - HQ has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0898-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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