Manufacturer
26 recalls in our database name Basic Reset Inc. as the manufacturing or recalling firm.
Of the 26 recalls from Basic Reset Inc. we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1 (4%) are Severe.
Which agencies issued them
The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.
Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.
Basic Reset Inc. is recalling AquaLyte dietary supplements because they do not conform to Dietary Supplement CGMP regulations. The product was distributed to all 50 states and several foreign countries.
Basic Reset Inc. is recalling 262 bottles of Beta Factor dietary supplement because the product does not conform to Dietary Supplement CGMP regulations.
Basic Reset Inc. is recalling 1,980 canisters of Vibrant Energy Drink because the products do not conform to Dietary Supplement CGMP regulations.
Basic Reset Inc. is recalling Bee Gold dietary supplements because they do not conform to Dietary Supplement CGMP regulations.
Basic Reset Inc. is recalling Dino Min dietary supplements because they do not conform to Dietary Supplement CGMP regulations. The product was distributed to all 50 states and several foreign countries.
Basic Reset Inc. is recalling Ionyte 4 fl. oz. bottles because the products do not conform to Dietary Supplement CGMP regulations.
Basic Reset Inc. is recalling Trim Up dietary supplement bottles because they do not conform to Dietary Supplement CGMP regulations.
Basic Reset Inc. is recalling pH-FX dietary supplements because they do not conform to Dietary Supplement CGMP regulations. The product was distributed to all 50 states and several foreign countries.
Basic Reset Inc. is recalling SlimUp dietary supplements because they do not conform to Dietary Supplement CGMP regulations. The product was distributed to all 50 states and several foreign countries.
Basic Reset Inc. is recalling Mello-Tonin dietary supplements because they do not conform to Dietary Supplement CGMP regulations. The product was distributed to all 50 states and several foreign countries.
Basic Reset Inc. is recalling Body Mass Reset dietary supplements because they do not conform to Dietary Supplement CGMP regulations.
Basic Reset Inc. is recalling Q-min dietary supplements because they do not conform to Dietary Supplement CGMP regulations. The product was distributed to all 50 states and several foreign countries.
Basic Reset Inc. is recalling GH-C dietary supplements because they do not conform to Dietary Supplement CGMP regulations. The product was shipped to all 50 states and several foreign countries.
Basic Reset Inc. is recalling 6,887 cases of Vibrant Energy Drink 15 g foil pouches because the products do not conform to Dietary Supplement CGMP regulations.
Basic Reset Inc. is recalling Energy FX products because FDA determined the marketing claims rendered the product a medical device that was adulterated and misbranded.
Basic Reset Inc. is recalling 25 bottles of Biogenyx CBD Oil because the product was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Basic Reset Inc. is recalling 98 bottles of CBD Reset 750 because the product was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Basic Reset Inc. is recalling 391 bottles of CBD Reset 2400 because the product was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Basic Reset Inc. is recalling Biogenyx CBD Oil because it was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Basic Reset Inc. is recalling Biogenyx CBD Oil because it was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Basic Reset Inc. is recalling 1,000 bottles of Nuovi Skin Toner because the product was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Basic Reset Inc. is recalling 339 bottles of Nuovi Firming Masque because the product was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Basic Reset Inc. is recalling 554 bottles of CBD Reset 750 oil because the product was marketed without an approved FDA application.
Basic Reset Inc. is recalling Miracle Facelift Masque because it was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Basic Reset Inc. is recalling 949 bottles of Earth Wash Cleaner because the product was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).