Acorn Raspberry Creme Filled Cookie found in gift basket: #925 Bakery, Coffee & Cocoa Gift Collection
Summary
The FDA issued a Class I for Acorn Raspberry Creme Filled Cookie found in gift basket: #925 Bakery, Coffee & by Houdini Inc.. Reason: Undeclared allergens; tree nuts.
Details
Source
Food Recall
External ID
F-0595-2024
Action Date
2023-12-20
Status
Terminated
Category
food
Product Description
Acorn Raspberry Creme Filled Cookie found in gift basket: #925 Bakery, Coffee & Cocoa Gift Collection
Lot/Code Info: Gift lot codes: LC597449 and LC600895 Cookie lot code #106052023
Quantity Affected: 4,875 cookies/1,168 gifts (total)
Reason for Recall
Undeclared allergens; tree nuts
Distribution
U.S. distribution to the following: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, 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, WA, WI, WV and WY No foreign distribution.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-11-24
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 143 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-0595-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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