The Recall Desk

Manufacturer

Pharma-Natural Inc.

17 recalls in our database name Pharma-Natural Inc. as the manufacturing or recalling firm.

What the numbers show

Total
17
Critical
0
Severe
2
Most recent
2023-10-04

Of the 17 recalls from Pharma-Natural Inc. we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2 (12%) are Severe.

Which agencies issued them

About this listing

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.

1–17 of 17

  • ModerateFDA (Food)·F-1615-2023·2023-10-04

    Pharma Natural Biotin 5000 mcg Dietary Supplement Recalled for Sub-Potency

    Pharma-Natural Inc. is recalling Pharma Natural Biotin 5000 mcg dietary supplement (Lot PN10686, Exp. Date 01/24) distributed in Puerto Rico because FDA testing found the biotin content was below the detection limit.

    Product
    Pharma Natural, Biotin 5000 mcg, Maximum Strength, Dietary Supplement, 30 Tablets
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1498-2019·2019-07-31

    Pharma-Natural Recalls Double Tussin DM Due to Manufacturing Violations

    Pharma-Natural Inc. is recalling 500 bottles of Double Tussin DM because the product was manufactured with current good manufacturing practice violations.

    Product
    DOUBLE TUSSIN DM (Dextromethorphan Hbr 20 mg, Guaifenesin 300 mg) in each 5ml teaspoon, 4 FL OZ (120 mL) bottle, Distributed by: Pamby Dist., Miami, FL 33414, NDC 63708-121-04.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1507-2019·2019-07-31

    Pharma-Natural Recalls Workvie Pain Roll-On for Manufacturing Violations

    Pharma-Natural Inc. is recalling Workvie Instant Pain Relieving Roll On due to current good manufacturing practice deviations, including lack of process and cleaning validation.

    Product
    Workvie Instant Pain Relieving Roll On (Lidocaine HCL 4% + Menthol 1% & Arnica), 2.5oz (71 g) roll on bottle, Exclusively Distributed by: Marketite, LLC., Coral Gables, FL 33134, NDC 72393-201-25.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1493-2019·2019-07-31

    Pharma-Natural Recalls AbeeMed Cream Due to Manufacturing Violations

    Pharma-Natural Inc. is recalling AbeeMed cream because it was manufactured with current good manufacturing practice violations, including a lack of process and cleaning validation.

    Product
    AbeeMed cream (Menthol 1.48% and Histamine DHCL 0.05%), 2 OZ jar, Manufactured exclusively for: Cas, P.O. Box 520248, Miami, FL 33152, UPC 8 50993 00402 4.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1505-2019·2019-07-31

    Pharma-Natural Recalls SORBUGEN Cough Syrup Due to Manufacturing Violations

    Pharma-Natural Inc. is recalling 7,392 bottles of SORBUGEN cough syrup because the product was manufactured with current good manufacturing practice violations.

    Product
    SORBUGEN — SORBUGEN (DEXTROMETHORPHAN HYDROBROMIDE, GLYCEROL GUAIACOLATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1501-2019·2019-07-31

    Lido E.R. Lidocaine Cream Recalled for Manufacturing Violations

    Pharma-Natural Inc. is recalling Lido E.R. Lidocaine Cream due to current good manufacturing practice violations, including lack of process and cleaning validation.

    Product
    Lido E.R. (Lidocaine HCL 4%) Pain Relieving Topical Analgesic Cream, 4 oz (113 g) jar, Distributed by Diabetic Supply of Suncoast, Inc., P.O. Box 2102, Vega Alta, PR 00692, NDC 63788-115-04.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1497-2019·2019-07-31

    Pharma-Natural Recalls GENCONTUSS Cough Syrup Due to Manufacturing Violations

    Pharma-Natural Inc. is recalling 3,000 bottles of GENCONTUSS cough syrup because it was manufactured with current good manufacturing practice violations.

    Product
    GENCONTUSS — GENCONTUSS (CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1496-2019·2019-07-31

    Pharma-Natural Recalls Army Health Pain Reliever Gel Due to CGMP Violations

    Pharma-Natural Inc. is recalling Army Health Pain Reliever Gel with Curcumin because it was manufactured with current good manufacturing practice violations.

    Product
    ARMY HEALTH Pain Reliever Gel With CURCUMIN (Menthol 3.00%), 0.5 OZ jar, Manufactured exclusively for: Manufactured exclusively for: Crossover Telecom, LLC., P.O. Box 520248, Miami, FL 33122, UPC 8 50993 00461 1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1500-2019·2019-07-31

    FDA Recalls Dermanak Skin Cream Due to Manufacturing Violations

    Pharma-Natural Inc. is recalling Dermanak Skin Fade Cream because it was manufactured with current good manufacturing practice violations.

    Product
    Dermanak original crema blanqueador (Hydroquinone 2%) Skin Fade Cream, 2 OZ. (56.7 g) jar, Manufactured by: Pamby Distributors, Inc., Miami, FL 33126, NDC 63788-108-02.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1504-2019·2019-07-31

    Pharma-Natural Recalls Tusslin Cough Syrup Due to Manufacturing Violations

    Pharma-Natural Inc. is recalling Tusslin cough syrup because it was manufactured with current good manufacturing practice violations, including a lack of process validation.

    Product
    TUSSLIN (Dextromethorphan HBr, 28 mg; Guaifenesin, 388 mg; Phenylephrine HCl, 10 mg) in each 5 mL tsp, Grape Flavor, 16 Fl.oz. (474 mL) bottle, Kramer Novis, San Juan, PR 00917, NDC 52083-622-16.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1495-2019·2019-07-31

    FDA Recalls Oliver's Harvest CBD+Lidocaine Cream for Manufacturing Violations

    Pharma-Natural Inc. is recalling Oliver's Harvest CBD+Lidocaine HCL 4% Pain Relief Cream due to current good manufacturing practice violations, including lack of process and cleaning validation.

    Product
    Oliver's Harvest CBD+Lidocaine HCL 4% Pain Relief (Lidocaine HCL 4%) Topical Analgesic Cream, 4 OZ (113.4 g) bottle with pump, Distributed by: Coast to Coast Natural, Inc., Wellington, FL 33414, NDC 63766-119-04.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1503-2019·2019-07-31

    Pharma-Natural Recalls Dayma Pain Gel for Manufacturing Violations

    Pharma-Natural Inc. is recalling 1,000 jars of Dayma SUPER FORTE XL10 Pain Relieving Topical Analgesic Gel due to current good manufacturing practice violations.

    Product
    Dayma SUPER FORTE XL10 (Camphor 0.5%, Menthol 2%, Methyl Salicylate 2%) Pain Relieving Topical Analgesic Gel, 4 Oz (113.4 g) jar, Distributed by: Biosfera International Distribution, LLC., Miami Lakes, FL 33016, NDC 63788-118-04.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1506-2019·2019-07-31

    Pharma-Natural Recalls NEOGEN-D Cough Syrup Due to Manufacturing Violations

    Pharma-Natural Inc. is recalling 2,052 bottles of NEOGEN-D cough syrup because the product was manufactured with current good manufacturing practice violations, including a lack of process and cleaning validation.

    Product
    NEOGEN-D (Dextromethorphan HBr, 30 mg; Guaifenesin, 200 mg; Phenylephrine HCl, 7.5 mg) in each 5 mL tsp, Raspberry Flavor, 16 fl oz (473 mL) bottle, Manufactured in the USA for Kramer Novis, San Juan, PR 00917, NDC 52083-699-16.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1502-2019·2019-07-31

    Pharma-Natural Recalls Lid O Creme Due to Manufacturing Violations

    Pharma-Natural Inc. is recalling Lid O Creme topical analgesic cream because it was manufactured with current good manufacturing practice violations, including lack of process validation.

    Product
    Lid O Creme (Lidocaine HCL 4% and Menthol 1%) Topical Analgesic Cream, 2.5 Oz (71 g) roll on bottle, Manufactured & Distributed by: Pharma Natural, Inc. Hialeah, FL 33016, NDC 63788-111-25.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1494-2019·2019-07-31

    Pharma-Natural Recalls Army Health Pain Reliever Roll-On for CGMP Violations

    Pharma-Natural Inc. is recalling Army Health Pain Reliever Roll-On bottles due to manufacturing process violations. The product was distributed in Florida and Texas.

    Product
    ARMY HEALTH With CURCUMIN (Menthol 3.00%) Pain Reliever Roll-On, 2.5 FL OZ (73ML) roll on bottle, Manufactured exclusively for: Crossover Telecom, LLC., P.O. Box 520248, Miami, FL 33122, UPC 8 50993 00408 6.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1492-2019·2019-07-31

    Pharma-Natural Recalls Oliver's Harvest CBD+Capsaicin Cream for CGMP Violations

    Pharma-Natural Inc. is recalling 998 bottles of Oliver's Harvest CBD+Capsaicin 0.2% Pain Relief Cream due to current good manufacturing practice violations.

    Product
    Oliver's Harvest CBD+Capsaicin 0.2% Pain Relief (Capsaicin 0.2%) Topical Analgesic Cream, 4 OZ (113.4 g) bottle with pump, Distributed by: Coast to Coast Natural, Inc., Wellington, FL 33414, NDC 63788-120-04.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1499-2019·2019-07-31

    Pharma-Natural Recalls LidoAID Gel Due to Manufacturing Violations

    Pharma-Natural Inc. is recalling LidoAID topical analgesic gel because it was manufactured with current good manufacturing practice violations, including a lack of process and cleaning validation.

    Product
    LidoAID (Lidocaine HCL 4%) portable pain relieving TOPICAL ANALGESIC GEL, 0.17 Oz (4 g) roll on bottle, Distributed by: Diabetic Supply of Suncoast, Inc., dba Advocate Diabetes, PO Box 2102, Vega Alta, PR 00692, NDC 63788-114-04.
    Category
    Drug
    Distribution
    Distributed nationwide