The Recall Desk

Severity 2 of 5

Moderate recalls

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

What “moderate” means here

Severity 2 (Moderate) recalls cover minor labeling errors, low-risk contamination, and voluntary precautionary recalls. The agency's own classification is typically FDA Class III, or the issue is something like incomplete instructions or a small UPC mismatch where the product itself is safe but doesn't meet documentation requirements. Use the same brand-name product safely; follow the manufacturer's instructions for return or exchange if you want a refund.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

7151–7175 of 21595

  • ModerateFDA (Drugs)·D-1139-2020·2020-04-15

    Herbal Doctor Remedies Recalls Immune-2100 Capsules for CGMP Deviations

    Herbal Doctor Remedies is recalling Immune-2100 500mg capsules because they were found to be misbranded as unapproved new drugs due to CGMP deviations.

    Product
    Immune-2100, 500mg Capsules, 90-count bottles, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-1145-2020·2020-04-15

    Herbal Doctor Remedies Recalls Nasal Ez Capsules Due to Misbranding

    Herbal Doctor Remedies is recalling Nasal Ez capsules because they were found to be misbranded as unapproved new drugs.

    Product
    Nasal Ez, 500mg Capsules, 90-count bottles, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-1142-2020·2020-04-15

    Herbal Doctor Remedies Recalls Lupus Care for Unapproved New Drug Status

    Herbal Doctor Remedies is recalling Lupus Care because the product is misbranded as an unapproved new drug. The product was sold online in the US and internationally.

    Product
    Lupus Care, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-1172-2020·2020-04-15

    Herbal Doctor Remedies Recalls Worm Off Capsules Due to Misbranding

    Herbal Doctor Remedies is recalling Worm Off capsules because they are misbranded as unapproved new drugs. The products were sold online in the US and internationally.

    Product
    Worm Off, 500mg Capsules, 90-count bottles, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-1161-2020·2020-04-15

    Herbal Doctor Remedies Recalls Skin Moist Capsules for CGMP Deviations

    Herbal Doctor Remedies is recalling Skin Moist 500mg capsules because they were found to be misbranded as unapproved new drugs.

    Product
    Skin Moist, 500mg Capsules, 90-count bottles, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1655-2020·2020-04-15

    Biomet Recalls Hip Cement Spacer Molds Due to Cleaning Process Concerns

    Biomet, Inc. is recalling StageOne Hip Cement Spacer Molds because of a potentially insufficient cleaning process or inadequate monitoring of cleaning parameters.

    Product
    BIOMET StageOne, Hip Cement Spacer Mold w/Reinforcement, 13 X 145 MM, 57 MM, Silicone, Sterile, Item 431213.
    Category
    Medical Device
    Distribution
    49 states
  • ModerateFDA (Devices)·Z-1686-2020·2020-04-15

    Baxter Recalls GEM Microvascular Couplers Due to Labeling Mismatch

    Baxter Healthcare is recalling 209 GEM Microvascular Anastomotic Coupler Devices because the size labeling on the outer tray may not match the inner tray.

    Product
    GEM Microvascular Anastomotic Coupler Devices - Product Usage: s intended to be used in the anastomosis of veins and arteries normally encountered in microsurgical procedures only in the peripheral vascular system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1645-2020·2020-04-15

    Biomet Recalls Hip Stem Cement Spacer Molds Due to Cleaning Concerns

    Biomet is recalling 230,001 hip stem cement spacer molds due to potentially insufficient cleaning processes or inadequate monitoring of cleaning parameters.

    Product
    BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 13 X 145 MM, Silicone, Sterile, Item 431192.
    Category
    Medical Device
    Distribution
    49 states
  • ModerateFDA (Devices)·Z-1656-2020·2020-04-15

    Biomet Hip Cement Spacer Mold Recalled for Cleaning Process Concerns

    Biomet is recalling StageOne Hip Cement Spacer Molds due to potentially insufficient cleaning processes and inadequate process monitoring.

    Product
    BIOMET StageOne, Hip Cement Spacer Mold w/Reinforcement, 17 X 165 MM, 64 MM, Silicone, Sterile, Item 431217.
    Category
    Medical Device
    Distribution
    49 states
  • ModerateFDA (Drugs)·D-1170-2020·2020-04-15

    Vitiligo Off Ointment Recalled for Being an Unapproved New Drug

    Herbal Doctor Remedies is recalling Vitiligo Off Ointment because it is misbranded as an unapproved new drug.

    Product
    Vitiligo Off Ointment, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-1146-2020·2020-04-15

    Herbal Doctor Remedies Recalls New Life Due to Unapproved New Drug Status

    Herbal Doctor Remedies is recalling New Life because the product is misbranded as an unapproved new drug. The recall covers all lots within expiry sold online in the US and internationally.

    Product
    New Life, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-1129-2020·2020-04-15

    Herbal Doctor Remedies Recalls Hair Back Ex Due to Misbranding

    Herbal Doctor Remedies is recalling Hair Back Ex capsules because they are misbranded as unapproved new drugs.

    Product
    Hair Back Ex, 500mg Capsules, 90-count bottles, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-1143-2020·2020-04-15

    Herbal Doctor Remedies Recalls Max Slim Capsules for Misbranding

    Herbal Doctor Remedies is recalling Max Slim 500mg capsules because the products are misbranded as unapproved new drugs.

    Product
    Max Slim, 500mg Capsules, 90-count bottles, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-1171-2020·2020-04-15

    Herbal Doctor Remedies Recalls Voice Rescue Capsules Due to Misbranding

    Herbal Doctor Remedies is recalling Voice Rescue 500mg capsules because the products were found to be misbranded as unapproved new drugs.

    Product
    Voice Rescue, 500mg Capsules, 90-count bottles, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-1122-2020·2020-04-15

    Herbal Doctor Remedies Recalls Edema Off for CGMP Deviations

    Herbal Doctor Remedies is recalling Edema Off because the product was found to be misbranded as an unapproved new drug due to CGMP deviations.

    Product
    Edema Off, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-1105-2020·2020-04-15

    Herbal Doctor Remedies Recalls Acupuncture Products for Misbranding

    Herbal Doctor Remedies is recalling acupuncture products sold online in the US and internationally because they are misbranded as unapproved new drugs.

    Product
    Acupuncture, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1646-2020·2020-04-15

    Biomet Recalls Hip Stem Cement Spacer Molds Due to Cleaning Concerns

    Biomet, Inc. is recalling 230,001 units of StageOne Select Hip Stem Cement Spacer Molds due to potentially insufficient cleaning processes.

    Product
    BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 15 X 155 MM, Silicone, Sterile, Item 431193.
    Category
    Medical Device
    Distribution
    49 states
  • ModerateFDA (Drugs)·D-1158-2020·2020-04-15

    Herbal Doctor Remedies Recalls Skin De-Tag for Unapproved Drug Status

    Herbal Doctor Remedies is recalling Skin De-Tag because the product is misbranded as an unapproved new drug.

    Product
    Skin De-Tag, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-1127-2020·2020-04-15

    Fungo Lotion Recalled for Being an Unapproved New Drug

    Herbal Doctor Remedies is recalling Fungo Lotion because it is misbranded as an unapproved new drug.

    Product
    Fungo Lotion, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-1151-2020·2020-04-15

    Herbal Doctor Remedies Recalls Pimples Off Solution for Misbranding

    Herbal Doctor Remedies is recalling Pimples Off Solution because the product is misbranded as an unapproved new drug.

    Product
    Pimples Off Solution 60 ML, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600- 0808
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1644-2020·2020-04-15

    Biomet Hip Stem Cement Spacer Mold Recalled for Cleaning Process Concerns

    Biomet is recalling 230,001 units of StageOne Select Hip Stem Cement Spacer Molds due to potentially insufficient cleaning processes and inadequate monitoring.

    Product
    BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 11 X 135 MM, Silicone, Sterile, Item 431191.
    Category
    Medical Device
    Distribution
    49 states