Summary
The FDA issued a Class I for Ministry of Snacks Sweet and Savory Collection #8700 by Houdini Inc.. Reason: Potential Salmonella contamination of Quaker Oats Chewy Granola Bars packed in gift baskets..
Details
Source
Food Recall
External ID
F-0721-2024
Action Date
2024-01-24
Status
Terminated
Category
food
Product Description
Ministry of Snacks Sweet and Savory Collection #8700
Lot/Code Info: Gift lot codes LC 595922, LC 596339, LC 597305, LC 597306, LC 597910, LC601543 and LC 607376 For Quaker Oats Chewy Granola Bar Peanut Butter Chocolate Chip and Chocolate Chip lot codes are: Best before of Aug-02-2024 and any earlier dater
Quantity Affected: 926 units
Reason for Recall
Potential Salmonella contamination of Quaker Oats Chewy Granola Bars packed in gift baskets.
Distribution
U.S. distribution to the following: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, IA, ID, IL, IN. KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM. NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV and WY No foreign distribution.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-12-19
Company
Fullerton, CA
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 81 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Houdini Inc. has 10 FDA actions in our database, including 10 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 (Houdini Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Houdini Inc. have FDA actions?
Houdini Inc. has 10 FDA actions in our database, including 10 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0721-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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