Fire Roasted Half Moon Green Zucchini (McCain Foods) – quality control issue (2018)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Fire Roasted Half Moon Green Zucchini : Sold in 25 lb. and 1200 lb. packaging. Brand Name: Jon-Lin¿
Brand
McCain Foods USA
Lot Codes / Batch Numbers
All products shipped on or after January 1
Products Sold
All products shipped on or after January 1, 2016 Batch numbers: 1001737375 1001746832 1001877722 1002182996 1002255608 1002295640 1002332314 1002044746 1002060760 1002175954 1002205218 1002255607 1002275476 1002288983 1002688419 1001287428 1001592434 1001797353 1001553709 1002081582 1002116108 1002304167 1002376744 1002404838 1002436016 1002454906 1002532861 1002539947 1002700095 1002715214 1001620429 1001718880 1001719989 1001968899 1002135459 1002205219 1002715215 1002744330 1001600073 1001602926 1001620430
McCain Foods USA is recalling Fire Roasted Half Moon Green Zucchini : Sold in 25 lb. and 1200 lb. packaging. Brand Name: Jon-Li due to During an internal audit at the manufacturing location, it was discovered that finished product had been released on numerous occasions after receivin. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
During an internal audit at the manufacturing location, it was discovered that finished product had been released on numerous occasions after receiving presumptive positive test results for Listeria monocytogenes and Salmonella; confirmation was not conducted.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 6, 2026