Death Wish Nitro Cold Brew Coffee Recall: Clostridium Botulinum Risk
Death Wish Coffee recalls 11oz Nitro Cold Brew Coffee with potential Clostridium Botulinum risk. Consumers should check UPC 851552005599 for affected products.
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Potential for Clostridium Botulinum
Contact the company
What happened, in plain English
Death Wish Coffee is recalling 11-ounce Nitro Canned Cold Brew Coffee due to potential Clostridium Botulinum contamination. This bacteria can cause serious illness, so affected products should not be consumed. Read more at govinfonow.com/recall/20423-death-wish-nitro-cold-brew-coffee-recall-clostridium-botulinum-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/20423-death-wish-nitro-cold-brew-coffee-recall-clostridium-botulinum-risk · Updated October 7, 2026 · FDA enforcement record: FDA #F-0028-2018
Cite this page
“Death Wish Nitro Cold Brew Coffee Recall: Clostridium Botulinum Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/20423-death-wish-nitro-cold-brew-coffee-recall-clostridium-botulinum-risk. Based on FDA recall #F-0028-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0028-2018%22&limit=1).
Why it’s dangerous
Clostridium Botulinum is a bacteria that produces a toxin causing severe food poisoning. This product may contain the bacteria that can lead to serious illness if consumed.
Who’s affected
Owners of Death Wish Nitro Canned Cold Brew Coffee 11 oz with UPC 851552005599 are affected. Anyone who has consumed this product is at risk of serious illness.
How to tell if you have this one
Check for Death Wish Nitro Canned Cold Brew Coffee 11 oz with UPC 851552005599. All date codes on the product are part of the recall.
- Brand
Death Wish- Product
Death Wish Nitro Canned Cold Brew Coffee 11 oz UPC: 851552005599- Category
Food
What to do — step by step
Stop Using Now
Discard the affected product immediately as it may contain Clostridium Botulinum.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 11 months 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-0028-2018 (September 18, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0028-2018 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.