Brownie Points Schmurtle 2oz Packaged in food grade cellophane only used as gift basket filler - not sold individua
Summary
The FDA issued a Class II for Brownie Points Schmurtle 2oz Packaged in food grade cellophane only used as by Brownie Points LLC. Reason: Contains Statement on Label does not include all allergens - Peanuts.
Details
Source
Food Recall
External ID
F-0615-2022
Action Date
2022-02-02
Status
Terminated
Category
food
Product Description
Brownie Points Schmurtle 2oz Packaged in food grade cellophane only used as gift basket filler - not sold individually
Lot/Code Info: Lot Number: 754
Quantity Affected: 209 units
Reason for Recall
Contains Statement on Label does not include all allergens - Peanuts
Distribution
AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY
Type: Voluntary: Firm initiated
Recall Initiated: 2022-01-10
Company
Columbus, OH
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 117 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (Brownie Points LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Brownie Points LLC have FDA actions?
This is the only FDA action we have on record for Brownie Points LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0615-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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