The Crooked Row - Nkratable 4.5g per bite - 3 bites per pack
Summary
The FDA issued a Class II for The Crooked Row - Nkratable 4.5g per bite - 3 bites per pack by Cannihelp Hemp Co LLC dba The Crooked Row. Reason: Unapproved food additive: kratom.
Details
Source
Food Recall
External ID
F-1699-2023
Action Date
2023-10-11
Status
Terminated
Category
food
Product Description
The Crooked Row - Nkratable 4.5g per bite - 3 bites per pack
Lot/Code Info: Batch No. mc70mb8962823 Best By 07/06/24
Quantity Affected: 261 packs
Reason for Recall
Unapproved food additive: kratom
Distribution
Single retail consignee within TN
Type: Voluntary: Firm initiated
Recall Initiated: 2023-09-14
Company
Crossville, TN
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 163 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 (Cannihelp Hemp Co LLC dba The Crooked Row) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Cannihelp Hemp Co LLC dba The Crooked Row have FDA actions?
This is the only FDA action we have on record for Cannihelp Hemp Co LLC dba The Crooked Row in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1699-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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