Novacare, LLC

Complete recall history across all FDA and CPSC categories — 14 total recalls

Novacare, LLC appears in recall records across 2 categories. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Food Recalls (1)

FDA food safety enforcement actions by Novacare, LLC

Date Product Reason Class
May 27, 2015 Glucosamine 750 mg 120 ct, Capsule, Dosage: 12 capsules, 750 mg ea., three t... TSN Labs is conducting a field action on Glucosamine 750 mg 120 ct due to ina... Class II

Drug Recalls (13)

FDA drug safety enforcement actions by Novacare, LLC

Date Product Reason Class
Aug 24, 2015 Thin and Slim Burn Fat Now Dietary Supplement packaged in 90 capsule containe... Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence of... Class I
Aug 24, 2015 TruTrim (product not labeled) Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence of... Class I
Aug 24, 2015 Xcellerator (product not labeled) Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence of... Class I
Aug 24, 2015 The Store Thin and Slim Thermogenic Fat Burner Dietary Supplement packaged in... Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence of... Class I
Aug 24, 2015 Black Widow 25 Ephedra Super Potent Fat Burner Dietary Supplement packaged in... Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence of... Class I
Aug 24, 2015 Methyldrene Original 25 Ephedra ECA Stack Extra-Potent Fat Burner Dietary Sup... Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence of... Class I
Aug 24, 2015 MetaPro 360 Metabolic Accelerator Dietary Supplement packaged in 120 capsule ... Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence of... Class I
Aug 24, 2015 The People's Chemist Thermo FX Barely Legal Thermogenic Aid, packaged in 90 c... Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence of... Class I
Aug 24, 2015 Thin and Slim Extreme Stack Fat Burner Dietary Supplement packaged in 90 caps... Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence of... Class I
Aug 24, 2015 Thin and Slim Naturally The Natural Alternative AM Dietary Supplement package... Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence of... Class I
Aug 24, 2015 Thin and Slim Fataway Ultimate Stack with Chromium, packaged per 120 capsules... Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence of... Class I
Aug 24, 2015 Asia Black 25 Ephedra Extreme Fat Burner Potent Dietary Supplement packaged i... Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence of... Class I
Aug 24, 2015 Thin and Slim MaxOut Body Max Out FX Fat Burner with Ephedra packaged in cont... Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence of... Class I

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.

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