Bakemark Canada White Cross Topping Mix Recall: E. coli O121 Contamination Risk
Bakemark Canada recalls White Cross Topping Mix 10 lb due to potential E. coli O121 contamination. Consumers should avoid using affected lots.
Lower-risk recall
Product may be contaminated with E. coli O121.
Contact the company
What happened, in plain English
Bakemark Canada is recalling White Cross Topping Mix 10 lb products that may contain E. coli O121 bacteria. This contamination could cause foodborne illness if the product is consumed. Read more at govinfonow.com/recall/20839-bakemark-canada-white-cross-topping-mix-recall-e-coli-o121.
Source Summary by GovInfoNow · govinfonow.com/recall/20839-bakemark-canada-white-cross-topping-mix-recall-e-coli-o121 · Updated October 8, 2026 · FDA enforcement record: FDA #F-2138-2017
Cite this page
“Bakemark Canada White Cross Topping Mix Recall: E. coli O121 Contamination Risk.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/20839-bakemark-canada-white-cross-topping-mix-recall-e-coli-o121. Based on FDA recall #F-2138-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2138-2017%22&limit=1).
Why it’s dangerous
The product may be contaminated with E. coli O121 bacteria, which can cause food poisoning. This bacteria is typically spread through contaminated food and can lead to stomach cramps, diarrhea, and fever.
Who’s affected
Anyone who purchased the White Cross Topping Mix 10 lb from the listed lot numbers. People with compromised immune systems are at higher risk of foodborne illness.
How to tell if you have this one
Check the product label for the lot numbers 4-16-326-01 or 4-16-326-02. The product is a 10 lb White Cross Topping Mix with UPC 0 64278 50623 7.
- Brand
Bakemark Canada- Product
BAKEMARK CANADA White Cross Topping Mix 10 lb 4.54 kg; BakeMark NDS Item Code: 50623; UPC: 0 64278 50623 7- Category
Food
What to do — step by step
Check Product Label
Look for lot numbers 4-16-326-01 or 4-16-326-02 on the packaging.
Where it went and when
Where it was distributed
Distributed in Connecticut and New Jersey.
FDA distribution: “CT NJ” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Connecticut, New Jersey.
Recall timeline
FDA terminated this recall 58 days 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-2138-2017 (June 13, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2138-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 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.