Thistle Watermelon Berry Cold-Pressed Organic Juice watermelon strawberry lime chia 32 FL OZ (355 mL) Keep Refrigerated
Summary
The FDA issued a Class II for Thistle Watermelon Berry Cold-Pressed Organic Juice watermelon strawberry lime c by THISTLE HEALTH INC. Reason: Manufactured using organic strawberries potentially contaminated with Hep A..
Details
Source
Food Recall
External ID
F-1313-2022
Action Date
2022-06-22
Status
Terminated
Category
food
Product Description
Thistle Watermelon Berry Cold-Pressed Organic Juice watermelon strawberry lime chia 32 FL OZ (355 mL) Keep Refrigerated Distributed By: Thistle Health, Inc., Vacaville, CA 95688
Lot/Code Info: Lot 76 Code Date 6/12/22
Quantity Affected: 965 bottles
Reason for Recall
Manufactured using organic strawberries potentially contaminated with Hep A.
Distribution
U.S. distribution to the following: CA, NV, OR, WA No foreign distribution.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-05-31
Company
Vacaville, 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 175 food recalls issued in the same week, part of 204 food-related FDA actions this month.
THISTLE HEALTH INC has 2 FDA actions in our database, including 2 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 (THISTLE HEALTH INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does THISTLE HEALTH INC have FDA actions?
THISTLE HEALTH INC has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1313-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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