True Goodness by Meijer Oat-Based Plain Yogurt Alternative, 24oz plastic tub, UPC: 7-13733-03918-5
Summary
The FDA issued a Class II for True Goodness by Meijer Oat-Based Plain Yogurt Alternative, 24oz plastic tub, UP by Meijer Inc. Reason: almond-based product was packaged in tubs labeled as oat-based with almond based lid.
Details
Source
Food Recall
External ID
F-0246-2023
Action Date
2023-01-18
Status
Terminated
Category
food
Product Description
True Goodness by Meijer Oat-Based Plain Yogurt Alternative, 24oz plastic tub, UPC: 7-13733-03918-5
Lot/Code Info: Lot | Date Code: #2002 | 21 DEC 2022
Quantity Affected: 1,590 tubs
Reason for Recall
almond-based product was packaged in tubs labeled as oat-based with almond based lid
Distribution
IL, IN, KY, MI, OH, WI
Type: Voluntary: Firm initiated
Recall Initiated: 2022-12-16
Company
Grand Rapids, MI
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 49 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Meijer Inc has 18 FDA actions in our database, including 18 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 (Meijer Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Meijer Inc have FDA actions?
Meijer Inc has 18 FDA actions in our database, including 18 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0246-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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