1. TNVitamins Ultrapotent Complete Green Superfood Recall: What To Do

Total nutrition recall notices went out to consumers in June 2026. The U.S. Food and Drug Administration posted the action on June 17, 2026. Total Nutrition Inc recalled two moringa capsule supplements. The agency says the products may be contaminated with Salmonella. Roughly 13,000 units fall inside the recall. The FDA assigned it recall number H-0942-2026. It carries a Class I severity classification. That is the agency’s most serious category. If green superfood capsules sit in your cabinet, read the label details below.

What the Total Nutrition Recall Covers

The total nutrition recall names two specific supplement products. The first is TNVitamins Ultrapotent Complete Green Superfood Moringa Capsules, sold in a 120 count bottle. The second is Doctor s Pride Complete Green Superfood Ultra Potent Moringa 10,000 mg, also sold in 120 capsules. Both are moringa-based green superfood supplements. The labels look different. However, the FDA listed both under the same recall action.

Product names on supplement bottles can run long. As a result, shoppers often remember only the brand. Read the full front panel before you decide you are safe. Look for the words “Complete Green Superfood” and “Moringa” together. Check the capsule count too. Both recalled items are 120-count bottles. If your label matches either description, treat the bottle as recalled.

The scope of the total nutrition recall is listed at 13,000 units. That figure counts bottles in the recalled distribution, not customers. One household may hold several bottles. In most cases, supplement recalls of this size reach multiple states. The agency record available here does not list specific lot codes, retailers, or sale dates. Do not assume your bottle is excluded because you cannot find a lot code.

The recall was dated June 17, 2026. Supplements typically carry long shelf lives. For example, a capsule bottle bought months ago may still be half full. That is why recalled supplements linger in homes far longer than fresh food. Check the official FDA notice linked on this page for any lot-level detail the agency publishes.

The Hazard and Reported Injuries

The hazard behind the total nutrition recall is possible Salmonella contamination. Salmonella is a bacterium that causes foodborne illness. The FDA classified this action as Class I. A Class I designation means the agency believes exposure could cause serious health consequences or death. That classification reflects the agency’s risk judgment. It is not a statement that anyone was hurt.

Salmonella infection usually shows up as diarrhea, fever, and stomach cramps. Symptoms typically begin six hours to six days after exposure. Most healthy adults recover within about a week. However, some people get much sicker. In severe cases, the bacteria can move from the intestines into the bloodstream. That can require hospital care.

Risk is not spread evenly across the population. Young children, adults over 65, and pregnant people face higher risk. So do people with weakened immune systems, including cancer patients and transplant recipients. Supplements are often taken daily by exactly these groups. For example, older adults frequently take greens capsules on a doctor’s suggestion. That overlap is part of why a Class I classification matters here.

The agency record for this total nutrition recall does not state whether any injuries or illnesses were reported. That silence cuts both ways. It does not confirm harm. It also does not confirm that nobody got sick. Be skeptical of any website that claims a confirmed illness count for this recall. Rely on the official FDA notice for updates.

What To Do If You Own This Product

Stop taking the product first. That is the single most important step in any total nutrition recall response. Do not finish the bottle to avoid waste. Do not give it to a family member. Do not donate it to a food pantry or shelter. A recalled supplement should leave the daily routine immediately.

Next, identify what you actually have. Take a clear photo of the front label, the back panel, and any lot or expiration code. Write down where and when you bought it. Keep the receipt or the online order confirmation if you can find it. Typically, this documentation matters more later than people expect. It is far easier to gather now than months from now.

Then follow the official instructions. The remedy terms for this total nutrition recall are set by the company and the FDA, and the notice linked below is the authoritative source. This article does not state what the remedy is. Read the official notice and do exactly what it says. If the notice lists a phone number or email for the company, use that channel first.

View the official FDA recall notice

Watch your health as well. If you took the product and feel sick, contact a healthcare provider. Tell them the exact product name and that it was recalled for possible Salmonella. Mention the recall number, H-0942-2026, if asked. In most cases, providers will want to know how much you took and when. Wash your hands after handling the bottle, and keep it away from food surfaces.

Does a Total Nutrition Recall Mean You Can Sue?

No. A total nutrition recall is a safety action, not a lawsuit. A recall is how a company and a regulator pull a product back from the market. It is administrative. Nobody has been found liable when a recall is announced. No court has ruled on anything. As of this writing, we have not verified any lawsuit filed over this specific recall.

A legal claim generally needs more than a defective or contaminated product. It typically needs an actual injury. It also needs causation, meaning a link between the product and the harm. A person who bought the capsules, never opened them, and never got sick usually has no personal injury claim. That is true even though the recall is real and serious.

If you did get sick, the picture changes. Documentation becomes the center of everything in a total nutrition recall injury claim. Medical records matter. Lab results identifying Salmonella matter a great deal. Proof of purchase matters. Any remaining product matters, so consider keeping the bottle sealed in a bag rather than discarding it, if the official notice allows that.

Talk to a licensed attorney in your state if you believe you were harmed. Depending on the facts, you may be eligible to pursue a claim. Nobody can promise a result, and this article does not. Deadlines called statutes of limitations apply, and they vary by state. As a result, waiting can quietly close a door that was open.

How Recalls Connect to Mass Tort Cases

Recalls and lawsuits are separate. However, they often intersect later. A recall notice creates a dated public record. It shows what the company knew, what the hazard was, and when regulators acted. In litigation, that record can become evidence. Plaintiffs’ lawyers frequently use recall timelines to argue a company knew about a risk before it warned the public.

The Philips CPAP litigation is a well-known example. Philips recalled millions of sleep apnea machines in June 2021 over degrading sound abatement foam. Thousands of lawsuits followed and were consolidated into multidistrict litigation. The recall itself was not the lawsuit. It was the starting gun that pushed regulators, journalists, and attorneys to look harder at the underlying problem.

Takata airbag inflators followed a similar arc. Recalls expanded over years and eventually covered tens of millions of vehicles. Litigation and a bankruptcy followed. In both examples, the pattern was the same. A safety action came first. Investigation came next. Legal claims came only for people who could show real injury and a real causal link.

Frequently Asked Questions

What products are covered by the total nutrition recall?

Two products are named. They are TNVitamins Ultrapotent Complete Green Superfood Moringa Capsules in 120 count, and Doctor s Pride Complete Green Superfood Ultra Potent Moringa 10,000 mg in 120 capsules. Both were recalled by Total Nutrition Inc under FDA recall number H-0942-2026.

Were any illnesses reported from these supplements?

The FDA record for this recall does not state whether illnesses or injuries were reported. That means no conclusion should be drawn in either direction. Check the official FDA notice for any updates the agency publishes.

How do I get a refund or replacement?

Follow the instructions in the official FDA notice linked on this page. The remedy terms come from the company and the agency, not from this article. Contact information for the recalling firm is typically included in that notice.

Were You Injured by a Recalled Product?

A recall by itself is a safety action, not a legal claim. However, if a recalled product caused a real injury, you may be eligible to pursue compensation. A licensed attorney can review your situation at no upfront cost — most work on contingency, meaning you pay nothing unless you recover.

Official Sources & Resources

Verify every recall against the issuing agency before acting:

• U.S. Food and Drug Administration: official recall database — the record of truth for this notice
• CPSC: cpsc.gov — household goods, toys, furniture, appliances
• FDA: fda.gov — food, drugs, and medical devices
• NHTSA: nhtsa.gov — vehicles, tires, and child car seats
• USDA FSIS: fsis.usda.gov — meat, poultry, and egg products

Content last reviewed July 2026. This is general educational information, not legal advice. If you notice outdated information, please contact us.

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• Tort Reform by State — 50-State Comparison

Attorney Advertising. The information on this page is provided for general informational purposes only and does not constitute legal advice. A product recall is a safety action by a manufacturer or regulator and does not by itself establish liability or create a legal claim. No attorney-client relationship is created by accessing or using this content. Every case is unique. If you believe you were harmed by a recalled product, consult a licensed attorney in your jurisdiction.