J.M. Smucker HUNGRY JACK Pancake Mix Recall: Salmonella Risk
J.M. Smucker recalls HUNGRY JACK Original Pancake & Waffle Mix due to salmonella contamination. Consumers should avoid using affected products to prevent foodborne illness.
Lower-risk recall
Product tested positive for salmonella.
Contact the company
What happened, in plain English
J.M. Smucker is recalling HUNGRY JACK Original Pancake & Waffle Mix because it tested positive for salmonella. This poses a risk of foodborne illness if the product is consumed. Read more at govinfonow.com/recall/19261-j-m-smucker-hungry-jack-pancake-mix-recall-salmonella-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/19261-j-m-smucker-hungry-jack-pancake-mix-recall-salmonella-risk · Updated October 7, 2026 · FDA enforcement record: FDA #F-1107-2018
Cite this page
“J.M. Smucker HUNGRY JACK Pancake Mix Recall: Salmonella Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19261-j-m-smucker-hungry-jack-pancake-mix-recall-salmonella-risk. Based on FDA recall #F-1107-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1107-2018%22&limit=1).
Why it’s dangerous
The product tested positive for salmonella, a bacterium that can cause food poisoning. Consuming contaminated food may lead to symptoms like diarrhea, fever, and stomach cramps. The risk is low for most people but can be more severe for vulnerable groups.
Who’s affected
Anyone who owns or uses the recalled HUNGRY JACK Original Pancake & Waffle Mix. Children and elderly individuals may be at higher risk due to increased vulnerability to foodborne illnesses.
How to tell if you have this one
Check for the product name 'HUNGRY JACK Original Pancake & Waffle Mix' with a net weight of 32 oz (2 lb) or 907 g. The recall includes specific lot numbers: 7331 501, 7332 501, and 7333 501.
- Brand
J.M. Smucker- Category
Food
What to do — step by step
Check Product Lot Number
Look for the lot numbers 7331 501, 7332 501, or 7333 501 on the product packaging.
Where it went and when
Where it was distributed
Distributed in 25 states.
FDA distribution: “Product was distributed in the following states: AL, CA, FL, HI, IA, IL, IN, KS, LA, MD, MI, MN, MO, MS, NC, ND, NE, NY, OH, OK, PA, TN, TX, VA & WI” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, California, Florida, Hawaii, Illinois, Indiana, Iowa, Kansas, Louisiana, Maryland, Michigan, Minnesota, Mississippi, Missouri, Nebraska, New York, North Carolina, North Dakota, Ohio, Oklahoma, Pennsylvania, Tennessee, Texas, Virginia, Wisconsin.
Recall timeline
FDA terminated this recall 2.3 years 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.
Questions people ask
What should I do if I have the recalled product?
Do not consume the product. Check the lot number to confirm if it is affected and contact J.M. Smucker for further instructions.
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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-1107-2018 (April 6, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1107-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 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.