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Pharma-Natural Inc.

Complete recall history across all FDA and CPSC categories — 17 total recalls

Recall Summary

1 Food Recalls 16 Drug Recalls

Pharma-Natural Inc. 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 Pharma-Natural Inc.

Date Product Reason Class
Aug 15, 2023 Pharma Natural, Biotin 5000 mcg, Maximum Strength, Dietary Supplement, 30 Tab... FDA sample analysis of Pharma Natural Biotin 5000 mcg Maximum Strength (30 ta... Class III

Drug Recalls (16)

FDA drug safety enforcement actions by Pharma-Natural Inc.

Date Product Reason Class
Jun 21, 2019 ARMY HEALTH With CURCUMIN (Menthol 3.00%) Pain Reliever Roll-On, 2.5 FL OZ (7... CGMP Deviations: products were manufactured with lack of process validation, ... Class II
Jun 21, 2019 Oliver's Harvest CBD+Capsaicin 0.2% Pain Relief (Capsaicin 0.2%) Topical Anal... CGMP Deviations: products were manufactured with lack of process validation, ... Class II
Jun 21, 2019 Dermanak original crema blanqueador (Hydroquinone 2%) Skin Fade Cream, 2 OZ. ... CGMP Deviations: products were manufactured with lack of process validation, ... Class II
Jun 21, 2019 NEOGEN-D (Dextromethorphan HBr, 30 mg; Guaifenesin, 200 mg; Phenylephrine HCl... CGMP Deviations: products were manufactured with lack of process validation, ... Class II
Jun 21, 2019 Lido E.R. (Lidocaine HCL 4%) Pain Relieving Topical Analgesic Cream, 4 oz (11... CGMP Deviations: products were manufactured with lack of process validation, ... Class II
Jun 21, 2019 TUSSLIN (Dextromethorphan HBr, 28 mg; Guaifenesin, 388 mg; Phenylephrine HCl,... CGMP Deviations: products were manufactured with lack of process validation, ... Class II
Jun 21, 2019 Lid O Creme (Lidocaine HCL 4% and Menthol 1%) Topical Analgesic Cream, 2.5 Oz... CGMP Deviations: products were manufactured with lack of process validation, ... Class II
Jun 21, 2019 Oliver's Harvest CBD+Lidocaine HCL 4% Pain Relief (Lidocaine HCL 4%) Topical ... CGMP Deviations: products were manufactured with lack of process validation, ... Class II
Jun 21, 2019 LidoAID (Lidocaine HCL 4%) portable pain relieving TOPICAL ANALGESIC GEL, 0.1... CGMP Deviations: products were manufactured with lack of process validation, ... Class II
Jun 21, 2019 SORBUGEN NR (Dextromethorphan HBr, 15 mg; Glyceryl Guaiacolate (Guaifenesin),... CGMP Deviations: products were manufactured with lack of process validation, ... Class II
Jun 21, 2019 Workvie Instant Pain Relieving Roll On (Lidocaine HCL 4% + Menthol 1% & Arnic... CGMP Deviations: products were manufactured with lack of process validation, ... Class II
Jun 21, 2019 AbeeMed cream (Menthol 1.48% and Histamine DHCL 0.05%), 2 OZ jar, Manufacture... CGMP Deviations: products were manufactured with lack of process validation, ... Class II
Jun 21, 2019 ARMY HEALTH Pain Reliever Gel With CURCUMIN (Menthol 3.00%), 0.5 OZ jar, Manu... CGMP Deviations: products were manufactured with lack of process validation, ... Class II
Jun 21, 2019 DOUBLE TUSSIN DM (Dextromethorphan Hbr 20 mg, Guaifenesin 300 mg) in each 5ml... CGMP Deviations: products were manufactured with lack of process validation, ... Class II
Jun 21, 2019 Dayma SUPER FORTE XL10 (Camphor 0.5%, Menthol 2%, Methyl Salicylate 2%) Pain ... CGMP Deviations: products were manufactured with lack of process validation, ... Class II
Jun 21, 2019 GENCONTUSS (Chlorpheniramine Maleate, 2mg; Dextromethorphan HBr, 10 mg; Pheny... CGMP Deviations: products were manufactured with lack of process validation, ... Class II

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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