Nova Products, Inc.

Complete recall history across all FDA and CPSC categories — 8 total recalls

Nova Products, Inc. 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 (8)

FDA drug safety enforcement actions by Nova Products, Inc.

Date Product Reason Class
Mar 28, 2014 MOJO RISEN ,670 mg, 2 capsule per pouch, Distributed by: Mojo Risen, LLC, Sp... Marketed Without an Approved NDA/ANDA; Nova Products, Inc. of Aston, Pennsylv... Class I
Mar 28, 2014 Xzen 1200, 750 mg, six capsules per bottle, Distributed by: xzen, City of Los... Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston, Pennsylv... Class I
Mar 28, 2014 XZEN GOLD,750 mg, six capsules per bottle, Distributed by: XZEN, City of Los ... Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston, Pennsylv... Class I
Mar 28, 2014 XZONE GOLD, 750 mg, one capsule blister pack, Distributed by: XZONE, Orland... Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston, Pennsylv... Class I
Mar 28, 2014 XZEN PLATINUM, 750 mg, 1 capsule per blister pack, Distributed by: XZEN, City... Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston, Pennsylv... Class I
Mar 28, 2014 Xzone 1200, 750 mg, one capsule per blister pack, Distributed by: Xzone, Orl... Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston, Pennsylv... Class I
Mar 28, 2014 Black Ant, 4600 mg, four capsules per box, , Manufacturer Timpo Bioengineerin... Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston, Pennsylv... Class I
Mar 28, 2014 AFRICAN BLACK ANT, 2800 mg, 6 capsules per box, produced by: Qinghan Hongw... Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston, Pennsylv... 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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