The Recall Desk

Hazard

Mis Labeling recalls

9,607 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,607
Critical
160
Severe
588
Most recent
2026-09-10

Of the 9,607 mis labeling recalls we have scored against our rubric, 160 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 588 (6%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all mis labeling recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

2101–2125 of 9607

  • HighFDA (Food)·F-0878-2020·2020-04-15

    FDA Recalls Nature's Earthly Choice Organic Lentil Trio for Gluten Contamination

    Global Juices & Fruits LLC is recalling Nature's Earthly Choice Organic Lentil Trio because the product tested positive for gluten and contained barley and wheat.

    Product
    Nature's Earthly Choice Organic Lentil Trio product containing a blend of red split, black and green lentils, labeled Gluten-Free, packaged in stand up resealable pouch, 12 oz. (340 g), UPC 6 79948 10006 8. The product's label is read in parts: "*** Gluten-Free *** ORGANIC LEN
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0879-2020·2020-04-15

    Audrey's Chia Cookies Recalled for Undeclared Milk Allergen

    Health Harvest, LLC is recalling Audrey's Chia Cookies Chocolate Chip due to undeclared milk allergen. The product was distributed in Arizona and California.

    Product
    Audrey's Chia Cookies Chocolate Chip, 4 OZ flexible pouch packaging, UPC Code: 858652007003, Manufactured for Health Harvest, LLC, P.O. Box 20634, Mesa, AZ 85277. 12 pouches/case.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1674-2020·2020-04-15

    Beckman Coulter MicroScan PROMPT Inoculation System-D Recalled for Incorrect Wands

    Beckman Coulter is recalling 3,472 units of the MicroScan PROMPT Inoculation System-D because they contain incorrect prompt wands, which may cause inaccurate antimicrobial susceptibility test results.

    Product
    Beckman Coulter MicroScan PROMPT Inoculation System-D, Catalog Number B1026-10D, UDI: 15099590659561 - Product Usage: The Prompt Inoculation System-D is used to standardize inocula for microdilution antimicrobial susceptibility test.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0881-2020·2020-04-15

    Audrey's Chia Cookies Lemon Recalled for Undeclared Milk Allergen

    Health Harvest, LLC is recalling Audrey's Chia Cookies Lemon due to undeclared milk allergen. The product was distributed in Arizona and California.

    Product
    Audrey's Chia Cookies Lemon, 4 OZ flexible pouch packaging, UPC Code: 858652007010, Manufactured for Health Harvest, LLC, P.O. Box 20634, Mesa, AZ 85277. 12 pouches/case.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-1111-2020·2020-04-15

    Herbal Doctor Remedies Recalls Asthma Chest Rub for Misbranding

    Herbal Doctor Remedies is recalling Asthma Chest Rub because the product is misbranded as an unapproved new drug.

    Product
    Asthma Chest Rub, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-1136-2020·2020-04-15

    Herbal Doctor Remedies Recalls Herpes V Balm for Unapproved New Drug Status

    Herbal Doctor Remedies is recalling Herpes V Balm because the product is misbranded as an unapproved new drug. The balm was sold online in the US and internationally.

    Product
    Herpes V Balm, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-1162-2020·2020-04-15

    Herbal Doctor Remedies Recalls Sperm Booster for Misbranding

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

    Product
    Sperm Booster, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-1164-2020·2020-04-15

    Herbal Doctor Remedies Recalls Sugar Off Capsules Due to Misbranding

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

    Product
    Sugar 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-1120-2020·2020-04-15

    Herbal Doctor Remedies Recalls Detoxin-S Capsules Due to CGMP Deviations

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

    Product
    Detoxin-S, 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-1147-2020·2020-04-15

    Herbal Doctor Remedies Recalls Pain Away Capsules for CGMP Deviations

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

    Product
    Pain Away, 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-1676-2020·2020-04-15

    Zimmer Oscillating Saw Blade Recalled for Incorrect Width Labeling

    Synvasive Technology is recalling 266 Zimmer oscillating saw blades because the label indicates a width of 25 mm, but the actual blade width is 19 mm.

    Product
    ZIMMER Oscillating Saw Blade -Cutting 75mm x 19mm x 1.00/1.27mm.intended for bone or cartilage in orthopedic procedures. Manufactured By: Synvasive Technology, Inc., a Subsidiary of Zimmer
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-1160-2020·2020-04-15

    Herbal Doctor Remedies Recalls Skin Lift Balm for Unapproved New Drug Status

    Herbal Doctor Remedies is recalling Skin Lift Balm because the product is misbranded as an unapproved new drug. The balm was sold online in the US and internationally.

    Product
    Skin Lift Balm, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-1163-2020·2020-04-15

    Herbal Doctor Remedies Recalls Stomach Cleanser Capsules for CGMP Deviations

    Herbal Doctor Remedies is recalling Stomach Cleanser capsules because the products were found to be misbranded as unapproved new drugs.

    Product
    Stomach Cleanser, 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-1125-2020·2020-04-15

    Fungo Balm Recalled for Being an Unapproved New Drug

    Herbal Doctor Remedies is recalling Fungo Balm because the product is misbranded as an unapproved new drug.

    Product
    Fungo Balm, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1687-2020·2020-04-15

    Baxter Recalls GEM Microvascular Couplers Due to Labeling Mismatch

    Baxter Healthcare is recalling 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 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 (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-1148-2020·2020-04-15

    FDA Recalls Pain Stopper Capsules Due to Unapproved New Drug Status

    Herbal Doctor Remedies is recalling Pain Stopper 500mg capsules because they are misbranded as unapproved new drugs.

    Product
    Pain Stopper, 500mg Capsules, 90-count bottle, 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-1130-2020·2020-04-15

    Herbal Doctor Remedies Recalls Hair Back Lotion for Unapproved New Drug Status

    Herbal Doctor Remedies is recalling Hair Back Lotion because the product is misbranded as an unapproved new drug. The lotion was sold online in the U.S. and internationally.

    Product
    Hair Back Lotion, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-1107-2020·2020-04-15

    Acne Off Recalled for CGMP Deviations and Misbranding as Unapproved New Drug

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

    Product
    Acne Off, 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 (Drugs)·D-1124-2020·2020-04-15

    Herbal Doctor Remedies Recalls Flare Off Capsules Due to Misbranding

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

    Product
    Flare 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-1144-2020·2020-04-15

    Herbal Doctor Remedies Recalls Metabolic Booster Capsules for Misbranding

    Herbal Doctor Remedies is recalling Metabolic Booster 500mg capsules because they are misbranded as unapproved new drugs.

    Product
    Metabolic Booster. 500mg Capsules, 90-count bottles, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    0 states