PLANET OAT Chocolate Chip Cookie Dough; OATMILK NON-DAIRY FROZEN DESSERT WITH COOKIE DOUGH & CHOCOLATE FLAVORED CHIPS
Summary
The FDA issued a Class II for PLANET OAT Chocolate Chip Cookie Dough; OATMILK NON-DAIRY FROZEN DESSERT WITH CO by HP Hood LLC. Reason: Product may contain undeclared peanuts..
Details
Source
Food Recall
External ID
F-1265-2022
Action Date
2022-06-15
Status
Terminated
Category
food
Product Description
PLANET OAT Chocolate Chip Cookie Dough; OATMILK NON-DAIRY FROZEN DESSERT WITH COOKIE DOUGH & CHOCOLATE FLAVORED CHIPS
Lot/Code Info: Best By Date 12/17/22; UPC 44100709906; Item No: 70990
Quantity Affected: 4,479 cases
Reason for Recall
Product may contain undeclared peanuts.
Distribution
FL, ME, CA, MA, CT, MD, LA, VT, PA, NY, OR, CO, ID
Type: Voluntary: Firm initiated
Recall Initiated: 2022-05-11
Company
Lynnfield, MA
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 197 food recalls issued in the same week, part of 204 food-related FDA actions this month.
HP Hood LLC has 15 FDA actions in our database, including 15 recalls.
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 (HP Hood LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does HP Hood LLC have FDA actions?
HP Hood LLC has 15 FDA actions in our database, including 15 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1265-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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