ANNOUNCED ONGOING Drug recall · Reported 12 Nov 2026 · FDA company announcement, classification pending
10 Day Forecast Capsules 3200mg recalled by Game Changer Products
Game Changer Products is recalling 10 Day Forecast Capsules 3200mg, distributed nationwide in the US. The recall was initiated on 12 Nov 2026 and is listed as ongoing.
Recall details
- Recall number
- FDA-PR-74323b963865
- Recalling firm
- Game Changer Products
- Brand
- 10 Day Forecast
- Classification
- Pending
- Status
- Ongoing
- Recall initiated
- 12 Nov 2026
- Reported
- 12 Nov 2026
- Reason category
- Hidden Drug Ingredients
- Drug class
- Pain Medication
Timeline
| 12 Nov 2026 | Recall initiated by company | |
| 12 Nov 2026 | Published in enforcement report | +0 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Tainted with Sildenafil and Acetaminophen. FOR IMMEDIATE RELEASE – November 12, 2026 - Tampa, Florida. Game Changer Products LLC is voluntarily recalling all lots of 10 Day Forecast capsules to the consumer level. FDA analysis has found the product to be tainted with sildenafil and acetaminophen. Sildenafil is an active ingredient in an FDA-approved prescription drug product, used to treat erectile dysfunction. Acetaminophen is a prescription and over-the-counter drug product used to temporarily relieve pain and reduce fever. Products containing sildenafil and acetaminophen cannot be marketed as dietary supplements. 10 Day Forecast capsules are unapproved new drugs for which safety and efficacy have not been established and, therefore, subject to recall. Risk Statement: Consumption of products with undeclared sildenafil may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may cause a significant drop in blood pressure that may be life threatening. People with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. Among the adult male population, who are most likely to use this product, those who use nitrates for cardiac conditions are most at risk. For patients already consuming acetaminophen products, unknowingly consuming additional acetaminophen, may result in life-threatening adverse events including liver damage, ranging from mild liver problems to complete liver failure and death, anaphylaxis and serious skin reactions. To date, Game Changer Prod
Products marketed as supplements sometimes contain undeclared prescription drug ingredients such as sildenafil or sibutramine. These can interact dangerously with other medicines.
Product as listed by the company
10 Day Forecast Capsules 3200mg
Where it was distributed
Nationwide
Nationwide MinnesotaPuerto Rico
Stores named: Online Retailers
Questions about this recall
Why was it recalled?
Tainted with Sildenafil and Acetaminophen. FOR IMMEDIATE RELEASE – November 12, 2026 - Tampa, Florida. Game Changer Products LLC is voluntarily recalling all lots of 10 Day Forecast capsules to the consumer level. FDA analysis has found the product to be tainted with sildenafil and acetaminophen. Sildenafil is an active ingredient in an FDA-approved prescription drug product, used to treat erectile dysfunction. Acetaminophen is a prescription and over-the-counter drug product used to temporarily relieve pain and reduce fever. Products containing sildenafil and acetaminophen cannot be marketed as dietary supplements. 10 Day Forecast capsules are unapproved new drugs for which safety and efficacy have not been established and, therefore, subject to recall. Risk Statement: Consumption of products with undeclared sildenafil may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may cause a significant drop in blood pressure that may be life threatening. People with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. Among the adult male population, who are most likely to use this product, those who use nitrates for cardiac conditions are most at risk. For patients already consuming acetaminophen products, unknowingly consuming additional acetaminophen, may result in life-threatening adverse events including liver damage, ranging from mild liver problems to complete liver failure and death, anaphylaxis and serious skin reactions. To date, Game Changer Prod
Where was it sold?
Nationwide
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does an unclassified recall mean?
The FDA assigns a class once it has assessed the health risk. Until then the recall is listed without one.
Read the official FDA notice · Source record retrieved 12 Nov 2026. This is a company announcement published by the FDA; the FDA has not yet classified the recall. The record is updated when the classification appears in the Enforcement Report. This page reports the record and gives no medical advice.