Summary
The FDA issued a Class II for Cerebelly Smart Bar; Apple Kale flavor; 5 pk and 7 pk; ambient storage by CEREBELLY INC. Reason: Surface mold visible on product.
Details
Source
Food Recall
External ID
F-0003-2024
Action Date
2023-10-04
Status
Terminated
Category
food
Product Description
Cerebelly Smart Bar; Apple Kale flavor; 5 pk and 7 pk; ambient storage
Lot/Code Info: Lots 23086BW (Mfg date 03/27/23; Exp date 12/22/23), 23083BW (Mfg date 03/24/23; Exp date 12/19/23), 23087BW (Mfg date 03/28/23; Exp date 12/23/23)
Quantity Affected: 152,655 (5pks) and 1,895 (7pks), total of 154,554 selling cartons for all products
Reason for Recall
Surface mold visible on product
Distribution
U.S. distribution to all 50 states and territories. No foreign distribution.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-09-11
Company
Los Gatos, CA
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 185 food recalls issued in the same week, part of 204 food-related FDA actions this month.
CEREBELLY INC has 4 FDA actions in our database, including 4 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 (CEREBELLY INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does CEREBELLY INC have FDA actions?
CEREBELLY INC has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0003-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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