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Dr. Ma's Laboratories Inc.

Hypericum Perforatum

LNHPD
23084919
Catalog
120
products
With avoid flag
0
products
FDA recalls
14
history
CAERS
0
reports
Recall historyObjective label signals
Flagged excipients
0
none
FDA recalls
14
14 Class I / II
CAERS reports
0
FDA consumer events
Certifications
0
none recorded
14 FDA recalls on file. · Every flag below links to the authority's published citation.

Supplement Facts

0 active ingredients
IngredientAmount% DV
Recall history

14 FDA recalls

  1. Class III2025-06-24brand-level

    Lithium Orotate, Weyland Brain Nutrition ; 60 vegetarian capsules, Dietary Supplement; Distributed by Enjoy Nutirtion, LLC. San Francisco, CA 94108, (415) 894-0537 2.5 mg UPC#: X001SBI13J 5 mg UPC#: X000PY16Z5 10 mg UPC#: X000T9B9B7 20 mg UPC#: X001VBLW8H 1000 MCG UPC#: X003SBV661

    Reason: Downstream recall of a dietary supplement ingredient that was manufactured out of specification.

    FDA record →
  2. Class III2025-06-24brand-level

    Lithium Orotate 2.5; 60 vegetarian capsules, Dietary Supplement; Distributed by Mecene LLC. 447 Sutter St., Suite 405, San Fransisco, CA 94108 2.5 mg UPC#: X002T4OPLL 10 mg UPC#: X0031AXVE9

    Reason: Downstream recall of a dietary supplement ingredient that was manufactured out of specifications.

    FDA record →
  3. Class II2021-10-06brand-level

    MidNite Tablet (Melatonin 1.5 mg) supplement, ULTRAtab Laboratories, Inc., Highland, NY

    Reason: cGMP Deviations

    FDA record →
  4. Class II2021-10-06brand-level

    Melatonin ER 5 mg caplet (supplement), ULTRAtab Laboratories, Inc., Highland, NY

    Reason: cGMP Deviations

    FDA record →
  5. Class II2021-10-06brand-level

    Melatonin ER 2 mg caplet (supplement), ULTRAtab Laboratories, Inc., Highland, NY

    Reason: cGMP Deviations

    FDA record →
  6. Class II2021-10-06brand-level

    Caffeine 150 mg with B6 and B12 vitamins (supplement), ULTRAtab Laboratories, Inc., Highland, NY

    Reason: cGMP Deviations

    FDA record →
  7. Class II2021-10-06brand-level

    Ephrine Plus Tablet (Caffeine 200 mg, Vitamin C 25 mg) Supplement, ULTRAtab Laboratories, Inc., Highland, NY

    Reason: cGMP Deviations

    FDA record →
  8. Class II2021-10-06brand-level

    Caffeine 125 mg with B6 and B12 vitamins (supplement), ULTRAtab Laboratories, Inc., Highland, NY

    Reason: cGMP Deviations

    FDA record →
  9. Class II2021-10-06brand-level

    Melatonin ER 0.5 mg caplet (supplement), ULTRAtab Laboratories, Inc., Highland, NY

    Reason: cGMP Deviations

    FDA record →
  10. Class II2021-10-06brand-level

    Caffeine 175 mg with B6 and B12 vitamins (supplement), ULTRAtab Laboratories, Inc., Highland, NY

    Reason: cGMP Deviations

    FDA record →
  11. Class III2020-03-24brand-level

    CALCI-MAX Dietary Supplement, 60 capsules, Manufactured for: DOMEL

    Reason: FDA sample analysis of Calci-Max lot 31453 showed the product zinc content to be 0.0% of label claim.

    FDA record →
  12. Class II2014-03-25brand-level

    OPTIMUM E-1000 IU Gluten Free Dietary Supplement 100 SOFTGELS Product is packaged in a white HDPE bottle with foil cap under the white plastic cap. Bottle contains 100 softgel caps. UPC 0 43292 56291 7.

    Reason: Magno Humphries Laboratories is recalling Vitamin E softgels because the principle display panel states the product contains 1000 IU of Vitamin E however the Supplement Facts label indicated 200 IU of Vitamin E. The supplement actually contains 1000 IU of Vitamin E.

    FDA record →
  13. Class I2012-06-04brand-level

    Product is a liquid dietary supplement packaged in white plastic bottles with a shrink wrap sleeve label. The product comes in 3 sizes, 2 oz, 16oz. and 33.8oz. The product label reads in part: "Fast Absorbing Liquid 1-OZ A DAY***WELLESSE***Digestive 3-in-1 Health Soluble Fiber Prebiotics Aloe Vera Promotes Gentle Regularity Supports Health Bacteria Balances Stomach Acidity***Isomaltooligosaccha

    Reason: Product ("Digestive 3 in 1 Health") was manufactured using a raw ingredient that tested positive for Salmonella by the raw ingredient supplier.

    FDA record →
  14. Class II2009-12-08brand-level

    Dietary supplement. Product is labeled as :" Rescue Me***911 Damage Control***brantley living herbal formulas***HERBAL SUPPLEMENT 15 INDIVIDUAL PACKETS 4 VEGAN CAPSULES PER PACKET (2-368mg/2-584mg Each)***DISTRIBUTED EXCLUSIVELY BY: Living Herbal Pharmacy, LLC PO Box 56-2410, Miami, FL 33256-2410***".

    Reason: The firm recalled because the product lot contained mispackaged product wherein some capsules were missing from the finished packaged product.

    FDA record →