supplementhackr
Herbal Fx

LumbarGarde

Serving
3 Capsule(s)
Form
capsule-unknown
DSLD
239703
Formula hash
e4e7fa35ebd2
Brand context
Herbal Fx
Catalog
1
products
With avoid flag
0
products
FDA recalls
46
history
CAERS
35
reports
Recall historyObjective label signals
Flagged excipients
0
none
FDA recalls
20
20 Class I / II
CAERS reports
35
FDA consumer events
Certifications
0
none recorded
20 FDA recalls on file. · Every flag below links to the authority's published citation.

Supplement Facts

1 active ingredients
IngredientAmount% DV
Proprietary Blend
Proprietary Blend (Combination)other
1350 mg—
Recall history

20 FDA recalls

  1. Class II2020-06-30brand-level

    "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***WHITE JOINTA***1 oz.***USES: NERVES, COLD, ASTHMA, BRONCHITIS, MUCOUS FEVER MENSTRUAL PROBLEMS***"; packaged in clear plastic zip-top bags

    Reason: Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

    FDA record →
  2. Class II2020-06-30brand-level

    "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***DOG BLOOD***1 oz.***USES: FIBROIDS, CYST, CLEANS WOMB, WOMAN IMBALANCE, PREVENT MISCARRIAGE***"; packaged in clear plastic zip-top bag

    Reason: Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

    FDA record →
  3. Class II2020-06-30brand-level

    "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***WHITE SAGE***2 oz.***USES: EXCESS SWEATING, FEMALE HORMONE, SINUS INFECTION, INDIGESTION, KILLS BACTERIA***"; packaged in clear plastic zip-top bags

    Reason: Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

    FDA record →
  4. Class II2020-06-30brand-level

    "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***BREAD NUT***1oz.***USES: CHOLESTEROL, OMEGA 3, BI POLAR, ANTIOXIDANT, BUILDS BONES, ACNE***"

    Reason: Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

    FDA record →
  5. Class II2020-06-30brand-level

    "SUNDIAL***TRADITIONAL HERBAL FORMULA***Flu-Allergies HayFever***" packaged in boxes

    Reason: Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

    FDA record →
  6. Class II2020-06-30brand-level

    "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***QUASSIA WOOD***2 oz.***USES: ALCOHOLISM, LIVER, STOMACH COMPLAINTS, DIGESTIVE SYSTEM, KILLS LICE & PARASITES***"; packaged in clear plastic zip-top bags

    Reason: Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

    FDA record →
  7. Class II2020-06-30brand-level

    "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***CINNAMON***1 oz.***USES: STOMACH PAIN, MUCOUS CONGESTION, COLDS, NOSE BLEED, STIMULANT, FLAVORING***"; packaged in clear plastic zip-top bags

    Reason: Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

    FDA record →
  8. Class II2020-06-30brand-level

    "SUNDIAL***TRADITIONAL HERBAL FORMULA***BLOOD PRESSURE***" packaged in boxes

    Reason: Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

    FDA record →
  9. Class II2020-06-30brand-level

    "SUNDIAL***TRADITIONAL HERBAL FORMULA***HEART***" packaged in boxes

    Reason: Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

    FDA record →
  10. Class II2020-06-30brand-level

    "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***BITTER WOOD***2 oz.***USES: EXPELS WORMS IN THE WEST INTESTINES, DESTROYS PARASITES, LEUKEMIA, DESTROY APPETITE FOR ALCOHOL***"

    Reason: Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

    FDA record →
  11. Class II2020-06-30brand-level

    "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***MOJO BUSH***1 oz.***USES: SKIN, BLOOD PURIFIER, STOMACH & INTESTINAL CLEANSER, REMOVES PARASITES***"; packaged in clear plastic zip-top bags

    Reason: Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

    FDA record →
  12. Class II2020-06-30brand-level

    "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***KING OF THE FOREST***1 oz.***USES: HYPERTENSION, ASTHMA, THROAT, KIDNEY, LIVER SPOTS, HERPES RASHES***"; packaged in clear plastic zip-top bags

    Reason: Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

    FDA record →
  13. Class II2020-06-30brand-level

    "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***JACK IN THE BUSH***1oz.***USES: COLD MEDICINE (ESP. IN CHILDREN), CALMS THE NERVES, RELIEVES DEPRESSION***"; packaged in clear plastic zip-top bags

    Reason: Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

    FDA record →
  14. Class II2020-06-30brand-level

    "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***PURPLE SAGE***1 oz.***USES: DEPRESSION, INSECT BITES, INSOMNIA, RELIEVES CONGESTION***"; packaged in clear plastic zip-top bags

    Reason: Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

    FDA record →
  15. Class II2020-06-30brand-level

    "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***FIG LEAF***1oz.***USES: FIBER, CALCIUM, DIABETES, HIGH BLOOD PRESSURE, GENITAL WARTS, LIVER, ULCERS***"; packaged in clear zip-top bags

    Reason: Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

    FDA record →
  16. Class II2020-06-30brand-level

    "SUNDIAL***TRADITIONAL HERBAL FORMULA***ARTHRITIS***" packaged in boxes

    Reason: Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

    FDA record →
  17. Class II2020-06-30brand-level

    "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***RED WATER GRASS***1 oz.***USES: FEMALE PROBLEMS, FIBROIDS, INFERTILITY, HIGH BLOOD PRESSURE***" packaged in clear plastic zip-top bags

    Reason: Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

    FDA record →
  18. Class II2020-06-30brand-level

    "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***TRUMPET LEAF***1 oz.***USES: DIABETES, ASTHMA, CONGESTION, SKIN BATH, ULCERS, SORES, PARKINSON'S DISEASE, KIDNEY***"; packaged in clear plastic zip-top bags

    Reason: Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

    FDA record →
  19. Class II2020-06-30brand-level

    SUNDIAL Traditional Herbal Products***Mahogany Bark ***2 oz.***USES: BODY WEAKNESSES, MALE REPRODUCTIVE ORGANS, INFERTILITY***" packaged in zip-top plastic bag

    Reason: Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

    FDA record →
  20. Class II2020-06-30brand-level

    "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***GUINEA HEN WEED***1 oz.***USES: ARTHRITIS, RHEUMATISM, STIMULATE IMMUNE SYSTEM, FIGHTS CANCER CELLS, VIRUSES, YEAST***"; packaged in clear plastic zip-top bags

    Reason: Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

    FDA record →
FDA CAERS · adverse event context
35
consumer-submitted adverse event reports filed with the FDA CFSAN Adverse Event Reporting System mentioning this product or its brand.

CAERS reports are unverified consumer submissions — not adjudicated causality. Large well-known brands accumulate proportionally more reports simply due to broader use. About CAERS →

Chemically equivalent

Same formula, different brand

Products with identical sorted (ingredient, amount) tuples.