FDA Recall: Live it Up Super Greens Original and for Potential Foodborne Illness - Salmonella
Source: FDA
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FDA Recall: Live it Up Super Greens Original and for Potential Foodborne Illness - Salmonella

Live it Up January 15, 2026

Live it Up Super Greens Recall: Salmonella Contamination Risk (All Lots & Stick Packs)

Important safety alert: Do not consume any Live it Up Super Greens powder or single-serve sticks. Products with lot codes that start with “A” (pouches) or “3” (sticks) should be discarded and refunded immediately.

Why Live it Up Super Greens Are Being Recalled

Manufacturer Superfoods Inc.—doing business as Live it Up—has voluntarily recalled every flavor and package size of its Super Greens product line after routine testing and outbreak investigations revealed potential Salmonella contamination. The pathogen can cause serious gastrointestinal illness, particularly in children, older adults and anyone with a weakened immune system.

Recalled Product Details (All Flavors & Sizes)

  • Live it Up Super Greens Original, 8.5 oz pouch — UPC 860013190804
  • Live it Up Super Greens Original, 30 × 0.28 oz sticks — UPC 850077468063
  • Live it Up Super Greens Wild Berry, 8.5 oz pouch — UPC 860013190811
  • Live it Up Super Greens Wild Berry, 30 × 0.32 oz sticks — UPC 850077468070

Lot codes: All pouches beginning with “A” and all stick-pack boxes beginning with “3.” Printed expiration dates range from 08/2026 through 01/2028.

How to Confirm Your Live it Up Super Greens Is Affected

  • Identify green pouches or green-and-white stick-pack cartons.
  • Locate the lot code on the lower back panel; affected codes start with “A” (pouch) or “3” (sticks).
  • Cross-check the UPC and flavor against the list above.

Illnesses Linked to the Live it Up Super Greens Outbreak

As of 15 January 2026, the FDA and CDC have associated 45 confirmed illnesses and 12 hospitalizations nationwide with the recalled products. No deaths have been reported.

What Consumers Should Do Right Now

  • Stop using the product and dispose of it in a sealed bag so others (including pets) cannot access it.
  • Request a refund by emailing recall@artofenso.com. Include your name, order number and a photo of the product showing the lot code.
  • Contact a healthcare professional if you experience fever, diarrhea, nausea, vomiting or abdominal cramps after consuming Live it Up Super Greens.

Sources

Recall Images

Live it Up Super Greens Original front pouch
Source: FDA
Live it Up Super Greens Original back pouch showing lot code
Source: FDA
Live it Up Super Greens Wild Berry front pouch
Source: FDA
Live it Up Super Greens Wild Berry back pouch showing lot code
Source: FDA
Live it Up Super Greens Original stick-pack front
Source: FDA
Live it Up Super Greens Original stick-pack back
Source: FDA
Live it Up Super Greens Wild Berry stick-pack front
Source: FDA
Live it Up Super Greens Wild Berry stick-pack back
Source: FDA

Frequently Asked Questions

1. Which Live it Up Super Greens products are recalled?
All Original and Wild Berry pouches and stick packs with lot codes that start with “A” or “3” and expiration dates between 08/2026 and 01/2028.
2. Where can I find the lot code on Live it Up Super Greens?
The lot code is printed in black on the lower back of each pouch and on the bottom of every stick-pack carton.
3. What if I already consumed Live it Up Super Greens from a recalled lot?
Monitor for Salmonella symptoms (fever, diarrhea, nausea, vomiting or abdominal pain). Seek medical advice if you feel unwell and mention potential exposure to contaminated greens powder.
4. Are other Live it Up products affected by this recall?
No. The recall is limited to Live it Up Super Greens Original and Wild Berry in all sizes. No other Live it Up supplements have been implicated.
5. How do I claim a refund for Live it Up Super Greens?
Email recall@artofenso.com with your name, order number and a photograph clearly showing the product and lot code.
6. How many illnesses are linked to Live it Up Super Greens so far?
As of 15 January 2026, authorities have confirmed 45 illnesses and 12 hospitalizations connected to the recalled product.

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