L'Bri Aloe Juice Recall: Undeclared Sodium Metabisulfite Hazard
L'Bri recalls Pure N' Natural Nutri Aloe Health Juice due to undeclared sodium metabisulfite. Check lot numbers and expiration dates for affected units.
Use caution until it’s fixed
Product contains ingredients that are not on the label including sodium metabisulfite, to which a part of the population may be sensitive.
Contact the company
What happened, in plain English
Cosmetic Labs LP is recalling L'Bri Pure N' Natural Nutri Aloe Health Juice Drink because it contains sodium metabisulfite, an ingredient not listed on the label. This poses a risk to individuals who may be sensitive to sulfites. The recall covers specific lots distributed nationwide in early 2016. Read more at govinfonow.com/recall/25137-l-bri-aloe-juice-recall-undeclared-sodium-metabisulfite-hazard.
Source Summary by GovInfoNow · govinfonow.com/recall/25137-l-bri-aloe-juice-recall-undeclared-sodium-metabisulfite-hazard · Updated October 11, 2026 · FDA enforcement record: FDA #F-1045-2016
Cite this page
“L'Bri Aloe Juice Recall: Undeclared Sodium Metabisulfite Hazard.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/25137-l-bri-aloe-juice-recall-undeclared-sodium-metabisulfite-hazard. Based on FDA recall #F-1045-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1045-2016%22&limit=1).
Why it’s dangerous
The juice contains sodium metabisulfite which is not declared on the ingredient label. People who are sensitive to sulfites may experience adverse reactions if they consume the product.
Who’s affected
Consumers who purchased L'Bri Pure N' Natural Nutri Aloe Health Juice Drink, particularly those with known sensitivities to sodium metabisulfite. The product was sold nationwide throughout the US.
How to tell if you have this one
Check for L'Bri Pure N' Natural Nutri Aloe Health Juice Drink in 960 mL (32 FL. OZ.) or 1 FL OZ./29 mL sizes. Affected lots include 401 5B, 414 1N, 426 3I, 444 2B, 444 2C, 444 2D, 505 2G, 517 3G, 517 3H, 517 3I, 517 3J, and 517 3K.
- Brand
L'Bri- Category
Food
What to do — step by step
Check Product Labels
Verify if your product matches the recalled lot numbers (401 5B, 414 1N, 426 3I, 444 2B, 444 2C, 444 2D, 505 2G, 517 3G, 517 3H, 517 3I, 517 3J, 517 3K).
Avoid Consumption If Sensitive
If you are sensitive to sodium metabisulfite, do not consume the product due to the undeclared ingredient.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide throughout the US” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 14 months after the firm started it.
- Firm started the recall
- FDA classified it Class III
- 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-1045-2016 (March 2, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1045-2016 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 11, 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.