Panera Bread Broccoli Cheddar Soup Recall: Foreign Object Hazard
Panera Bread recalls 48 oz. broccoli cheddar soup with foreign object risk. Check UPC 077958790918 for affected lots. Stop using if you have this product.
Lower-risk recall
Presence of Foreign object
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What happened, in plain English
Panera Bread is recalling broccoli cheddar soup due to a foreign object in the product. This could cause injury if the object is swallowed. Consumers should check the UPC code and lot numbers to see if they have the affected product. Read more at govinfonow.com/recall/22956-panera-bread-broccoli-cheddar-soup-recall-foreign-object-hazard.
Source Summary by GovInfoNow · govinfonow.com/recall/22956-panera-bread-broccoli-cheddar-soup-recall-foreign-object-hazard · Updated October 9, 2026 · FDA enforcement record: FDA #F-0475-2017
Cite this page
“Panera Bread Broccoli Cheddar Soup Recall: Foreign Object Hazard.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/22956-panera-bread-broccoli-cheddar-soup-recall-foreign-object-hazard. Based on FDA recall #F-0475-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0475-2017%22&limit=1).
Why it’s dangerous
The soup contains a foreign object that could be swallowed, leading to potential injury. This is a food safety hazard that requires immediate attention to prevent harm.
Who’s affected
Panera Bread customers who purchased the 48 oz. broccoli cheddar soup with UPC 077958790918 between specific dates. People who consume the soup are at risk if they have the foreign object.
How to tell if you have this one
Check the UPC code 077958790918 on the soup sleeve. Look for lot codes 092616-5F or 092616-6F. The product was sold refrigerated and expired by December 5, 2016.
- Brand
Panera Bread- Product
Panera Bread Broccoli Cheddar Soup, 48 oz. sleeve (2/24 oz. cups/sleeve). Refrigerated UPC Code: 077958790918- Category
Food
What to do — step by step
Check Product Details
Look for the UPC code 077958790918 and lot codes 092616-5F or 092616-6F on the soup sleeve.
Where it went and when
Where it was distributed
Distributed in 8 states.
FDA distribution: “CA, IL, IN, WY, FL, PA, CT, OK” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Connecticut, Florida, Illinois, Indiana, Oklahoma, Pennsylvania, Wyoming.
Recall timeline
FDA terminated this recall 40 days after the firm started it.
- Firm started the recall
- FDA classified it Class III
- 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-0475-2017 (November 2, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0475-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 9, 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.