Lower riskFood recall · FDA · Published November 5, 2019
Cain Food OXIBAKE YF: Possible Salmonella Contamination Risk
Cain Food Industries recalls OXIBAKE YF packaged in 50 lb. paper bags with polyethylene liners due to possible Salmonella contamination. Consumers should check lot numbers for affected products.
“Cain Food OXIBAKE YF: Possible Salmonella Contamination Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/16283-cain-food-oxibake-yf-possible-salmonella-contamination-risk. Based on FDA recall #F-0244-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0244-2020%22&limit=1).
Cain Food Industries, Inc. recalled OXIBAKE YF due to possible Salmonella contamination, the FDA said on Nov. 5, 2019. The voluntary Class I recall affects 1,000 pounds of product distributed in Michigan, Illinois, New York, Texas, Kansas, Arkansas, and North Carolina.
How to tell if you have it
Brand: Cain Food Industries
Product: OXIBAKE YF
Packaging: 50 lb. Multi-wall paper bag with polyethylene liner
Lot code: 215-19-0009
Quantity: 1,000 pounds
The hazard
The product poses a possible contamination with Salmonella. The FDA classified the recall as Class I.
Context
GovInfoNow's records show other recent recalls of similar products include Taylor Fresh Foods Diced Jalapenos Recall on Aug. 7, 2026, NatureBest Jalapeno Products Recall on Aug. 5, 2026, and Mellace Wegmans Mixed Nuts Recall on Dec. 2, 2025.
How to tell if you have this one
Check for OXIBAKE YF products in 50 lb. Multi-wall paper bags with polyethylene liners. The affected lot number is 215-1:0009.
Brand
Cain Food Industries
Category
Food
FDA recall event · 9 products
All 9 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 I
Status
Terminated
Distribution
MI, IL, NY, TX, KS, AR, NC
Recall number
Product, codes & lots
Quantity
F-0238-2020
Vitamin D2 Blend packaged in 50 lb. Multi-wall paper bag with polyethylene liner bags; lot 073-19-0017
2000 pounds
F-0239-2020
ASCORBO 150 POWDER packaged in 50 lb. Multi-wall paper bag with polyethylene liner; lot 265-19-0026
200 pounds
F-0240-2020
Ascorbo 160-2 Powder packaged in 50 lb. Multi-wall paper bag with polyethylene liner; lot 065-19-0008
50 pounds
F-0241-2020
BETA P-130 packaged in 50 lb. Multi-wall paper bag with polyethylene liner; lot 090-19-0003
2200 pounds
F-0242-2020
CDC-2010 packaged in 50 lb. Multi-wall paper bag with polyethylene liner; lot 047-19-0008
600 pounds
F-0243-2020
OXIBAKE CL packaged in 50 lb. Multi-wall paper bag with polyethylene liner; lot 218-19-0014
4000 pounds
F-0244-2020
OXIBAKE YF packaged in 50 lb. Multi-wall paper bag with polyethylene liner; lot 215-19-0009
1000 pounds
F-0245-2020
SLB-R POWDER packaged in 50 lb. Multi-wall paper bag with polyethylene liner; lot 242-19-0009
2000 pounds
F-0246-2020
TREM 21 POWDER packaged in 50 lb. Multi-wall paper bag with polyethylene liner; lot 068-19-0010
4000 pounds
Based on the official FDA remedy
What to do — step by step
Check Product Lot Number
Look for the lot number 215-19-0009 on the packaging.
Where it went and when
Where it was distributed
Distributed in 7 states.
Listed by the agency
Not listed
FDA distribution: “MI, IL, NY, TX, KS, AR, NC” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arkansas, Illinois, Kansas, Michigan, New York, North Carolina, Texas.
Recall timeline
FDA terminated this recall 5 months after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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-0244-2020 (November 5, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0244-2020 to see it in context.
Plain-language summary written by qwen3:4b on October 5, 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.