Fresh From Meijer, Turkey & Provolone Pretzel Roll Sliders, 6.4 Oz., Plastic clam-shell - clear lid, black bottom, UPC 7
Summary
The FDA issued a Class II for Fresh From Meijer, Turkey & Provolone Pretzel Roll Sliders, 6.4 Oz., Plastic cla by Meijer Inc. Reason: undeclared soy lecithin.
Details
Source
Food Recall
External ID
F-0077-2022
Action Date
2021-11-10
Status
Terminated
Category
food
Product Description
Fresh From Meijer, Turkey & Provolone Pretzel Roll Sliders, 6.4 Oz., Plastic clam-shell - clear lid, black bottom, UPC 7-13733-76500-8
Lot/Code Info: Best If Used By - 10/7 Best If Used By - 10/8 Best If Used By - 10/9 Best If Used By - 10/10 Best If Used By - 10/13 Best If Used By - 10/14 Best If Used By - 10/15 Best If Used By - 10/16
Quantity Affected: 9,516 units
Reason for Recall
undeclared soy lecithin
Distribution
Meijer retail locations and DCs in IL, IN, KY, MI, OH, WI
Type: Voluntary: Firm initiated
Recall Initiated: 2021-10-07
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 54 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-0077-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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