Meijer Recalls Honey Ham & Cheddar Pretzel Roll Sliders for Undeclared Soy
Meijer is recalling Fresh From Meijer Honey Ham & Cheddar Pretzel Roll Sliders due to undeclared soy lecithin. Check your fridge for affected lots.
Use caution until it’s fixed
undeclared soy lecithin
Contact the company
What happened, in plain English
Meijer Inc has recalled Fresh From Meijer Honey Ham & Cheddar Pretzel Roll Sliders because the product contains undeclared soy lecithin. This is a significant issue for anyone with a soy allergy, as they may not be aware of the allergen presence. The recall covers 10,212 units distributed across Meijer stores and distribution centers in Illinois, Indiana, Kentucky, Michigan, Ohio, and Wisconsin. Read more at govinfonow.com/recall/14031-meijer-recalls-honey-ham-cheddar-pretzel-roll-sliders-for-undeclared.
Source Summary by GovInfoNow · govinfonow.com/recall/14031-meijer-recalls-honey-ham-cheddar-pretzel-roll-sliders-for-undeclared · Updated October 10, 2026 · FDA enforcement record: FDA #F-0076-2022
Cite this page
“Meijer Recalls Honey Ham & Cheddar Pretzel Roll Sliders for Undeclared Soy.” GovInfoNow, updated October 10, 2026. https://govinfonow.com/recall/14031-meijer-recalls-honey-ham-cheddar-pretzel-roll-sliders-for-undeclared. Based on FDA recall #F-0076-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0076-2022%22&limit=1).
Why it’s dangerous
The product contains soy lecithin that was not listed on the ingredient label. For people with a soy allergy, consuming this undeclared allergen can trigger an allergic reaction ranging from mild symptoms to severe health complications.
Who’s affected
Consumers who purchased Fresh From Meijer Honey Ham & Cheddar Pretzel Roll Sliders at Meijer retail locations or received them from distribution centers in IL, IN, KY, MI, OH, and WI. Individuals with soy allergies are at the highest risk of an allergic reaction.
How to tell if you have this one
Check for Fresh From Meijer Honey Ham & Cheddar Pretzel Roll Sliders in a plastic clam-shell package with a clear lid and black bottom. The net weight is 6.24 Oz., and the UPC is 7-13733-76501-5. Verify the 'Best If Used By' date on the package, which will be one of: 10/7, 10/8, 10/9, 10/10, 10/13, 10/14, 10/15, or 10/16.
- Brand
Fresh From Meijer- Product
Fresh From Meijer, Honey Ham & Cheddar Pretzel Roll Sliders, 6.24 Oz., Plastic clam-shell - clear lid, black bottom- Category
Food
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
Meijer retail locations and DCs in IL, IN, KY, MI, OH, WI
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| F-0076-2022 | Fresh From Meijer, Honey Ham & Cheddar Pretzel Roll Sliders, 6.24 Oz., Plastic clam-shell - clear lid, black bottom, UPC 7-13733-76501-5; 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 | 10,212 units |
| F-0077-2022 | Fresh From Meijer, Turkey & Provolone Pretzel Roll Sliders, 6.4 Oz., Plastic clam-shell - clear lid, black bottom, UPC 7-13733-76500-8; 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 | 9,516 units |
What to do — step by step
Check Product Dates
Verify if your package has a 'Best If Used By' date between October 7 and October 16.
Stop Consumption
Do not eat the product if it matches the description and date range due to the undeclared soy allergen.
Return for Refund
The record does not specify a return location or refund process; please contact Meijer directly for instructions.
Where it went and when
Where it was distributed
Distributed in 6 states.
FDA distribution: “Meijer retail locations and DCs in IL, IN, KY, MI, OH, WI” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Illinois, Indiana, Kentucky, Michigan, Ohio, Wisconsin.
Recall timeline
FDA terminated this recall 4 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-0076-2022 (October 7, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0076-2022 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.