R Thomas Marketing, LLC

Complete recall history across all FDA and CPSC categories — 24 total recalls

R Thomas Marketing, LLC appears in recall records across 1 category. 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.

Drug Recalls (24)

FDA drug safety enforcement actions by R Thomas Marketing, LLC

Date Product Reason Class
Jan 9, 2016 Hard Ten Days, packaged in BIG BOX (6 small boxes / 6 capsules per box / 36 c... Marketed Without An Approved NDA/ANDA Class I
Jan 9, 2016 Bull's Genital, packaged in CASE (10 Cans / 10 capsules per can / 100 capsule... Marketed Without An Approved NDA/ANDA Class I
Jan 9, 2016 African Black Ant, packaged in 8 small boxes / 6 capsules per box / 48 capsul... Marketed Without An Approved NDA/ANDA Class I
Jan 9, 2016 Super Hard, packaged in BIG BOX (20 small boxes / 6 capsules per box / 120 ca... Marketed Without An Approved NDA/ANDA Class I
Jan 9, 2016 Bigger Longer More Time More Sperms, packaged in BIG BOX (6 small boxes / 6 c... Marketed Without An Approved NDA/ANDA Class I
Jan 9, 2016 Herb Viagra, packaged in Big Box (20 small boxes / 4 capsules per box / 80 ca... Marketed Without An Approved NDA/ANDA Class I
Jan 9, 2016 Germany Niubian, packaged in BIG BOX (10 small boxes / 24 capsules per box / ... Marketed Without An Approved NDA/ANDA Class I
Jan 9, 2016 Black Ant, packaged in Big Box (20 small boxes / 4 capsules per box / 80 caps... Marketed Without An Approved NDA/ANDA Class I
Jan 9, 2016 Mojo Risen, packaged in BIG BOX (24 individual cards / 2 capsules per card/ 4... Marketed Without An Approved NDA/ANDA Class I
Jan 9, 2016 Real Skill, packaged in 20 small boxes / 4 capsules per box / 80 capsules tot... Marketed Without An Approved NDA/ANDA Class I
Jan 9, 2016 Weekend Prince, packaged in 24 individual cards / 2 capsules per card/ 48 cap... Marketed Without An Approved NDA/ANDA Class I
Jan 9, 2016 Black Storm, packaged in SMALL BOX (6 capsules), Distributed by: R Thomas Mar... Marketed Without An Approved NDA/ANDA Class I
Jan 9, 2016 Zhen Gong Fu, packaged in BIG BOX (16 small boxes / 2 capsules per box / 32 c... Marketed Without An Approved NDA/ANDA Class I
Jan 9, 2016 Tiger King, packaged in BIG BOX (10 small bottles / 10 capsules per bottle / ... Marketed Without An Approved NDA/ANDA Class I
Jan 9, 2016 African Superman, packaged in BIG BOX (6 small boxes / 8 capsules per box / 4... Marketed Without An Approved NDA/ANDA Class I
Jan 9, 2016 Zhong Hua Niu Bian, packaged in BIG BOX (6 small boxes / 6 capsules per box /... Marketed Without An Approved NDA/ANDA Class I
Jan 9, 2016 Happy Passengers, packaged in BIG BOX (30 small boxes / 1 capsule per box / 3... Marketed Without An Approved NDA/ANDA Class I
Jan 9, 2016 Night Man, packaged in SMALL BOX (6 capsules), Distributed by: R Thomas Marke... Marketed Without An Approved NDA/ANDA Class I
Jan 9, 2016 Samurai-X, packaged in BIG BOX (24 individually wrapped capsules), Distribute... Marketed Without An Approved NDA/ANDA Class I
Jan 9, 2016 Bull, packaged in CASE (10 packs / 3 capsules per can / 30 capsules), Distrib... Marketed Without An Approved NDA/ANDA Class I
Jan 9, 2016 Man King, packaged in BIG BOX (8 small boxes / 5 capsules per box / 40 capsul... Marketed Without An Approved NDA/ANDA Class I
Jan 9, 2016 Plant Vigra, packaged in BIG BOX / (18 cans / 6 capsules per can / 108 capsul... Marketed Without An Approved NDA/ANDA Class I
Jan 9, 2016 Black Ant King, packaged in BIG BOX (10 capsules / can / 12 cans per box / 12... Marketed Without An Approved NDA/ANDA Class I
Jan 9, 2016 Stree Overlord, packaged in 10 small boxes / 1 capsule per box, Distributed b... Marketed Without An Approved NDA/ANDA 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.

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