Recall archive / FDA company announcement
Live it Up: Super Greens Original and Wild Berry Flavored pouches and packs — FDA announcement Jan 20, 2026
Published notice; closure not supplied
A company announcement posted by FDA. The listing date can differ from the original announcement date. The absence of a termination marker does not prove the recall is currently ongoing.
Source date Jan 20, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Super Greens Original and Wild Berry Flavored pouches and packs
- Reason
- Potential Foodborne Illness - Salmonella
- Classification
- Not supplied
- Recalling firm
- Superfoods, Inc. DBA as Live it Up
- Quantity
- Not supplied
- Agency-reported status
- Company recall announcement
- Source record identifier
- 96592977450b82de
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Live it Up Super Greens, NET WT 8.5oz (240g) with UPC 860013190804; Live it Up Super Greens, 30 – 0.28oz (8g) sticks, NET WT. 8.47oz (240g) with UPC 850077468063; Live it Up Super Greens, Wild Berry, NET WT 9.49oz (269.16g), with UPC 860013190811; Live it Up Super Greens, Wild Berry, 30 – 0.32oz (9g) Sticks, NET WT. 9.52oz (270g), with UPC 850077468070; The recalled products are packaged in green pouches. The lot code is printed on the bottom back of the packaging in black and begins with the letter “A” or the number “3” for a stick pack product. Additionally, the affected product has expiration dates from 08/2026 to 01/2028. Please see the example packaging and lot code below.; Customers who have purchased the affected product are asked to dispose of it immediately, do not eat, sell, or serve the product. Customers may request a refund by contacting Live it Up at [email protected] and provide your name, order number and a photo of the product with lot codes beginning with “A” and stick pack products. |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
The recalled product was sold to consumers located nationwide in the United States, including Puerto Rico, Guam, and Virgin Islands. Additionally, product was sold to consumers located in the United Kingdom. Products were sold through our direct-to-consumer website since September 2024 and on Amazon.com since July 30, 2025. We are also aware that there may be unauthorized 3rd party distribution to consumers through ebay.com, Walmart.com, or other sites.
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
- Alaska
- Alabama
- Arkansas
- Arizona
- California
- Colorado
- Connecticut
- Delaware
- Florida
- Georgia
- Hawaii
- Iowa
- Idaho
- Illinois
- Indiana
- Kansas
- Kentucky
- Louisiana
- Massachusetts
- Maryland
- Maine
- Michigan
- Minnesota
- Missouri
- Mississippi
- Montana
- North Carolina
- North Dakota
- Nebraska
- New Hampshire
- New Jersey
- New Mexico
- Nevada
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Rhode Island
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Virginia
- Vermont
- Washington
- Wisconsin
- West Virginia
- Wyoming
Dates in the source
- Fda listing date
- Jan 20, 2026
- Company announcement date
- Jan 15, 2026
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.