Frank s Red Hot Buffalo Ranch Seasoning 153g, Plastic Bottles, 36 packages per case
Summary
The FDA issued a Class I for Frank s Red Hot Buffalo Ranch Seasoning 153g, Plastic Bottles, 36 packages per by McCormick & Company - MSS - HQ. Reason: Product may be contaminated with Salmonella..
Details
Source
Food Recall
External ID
F-0900-2021
Action Date
2021-08-18
Status
Terminated
Category
food
Product Description
Frank s Red Hot Buffalo Ranch Seasoning 153g, Plastic Bottles, 36 packages per case
Lot/Code Info: UPC NUMBER: 066200021047 MCCORMICK ITEM NUMBER: 901543520 BB / MA 2022 SEP 06
Quantity Affected: 86 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-0900-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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