The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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126–150 of 810

  • CriticalFDA (Drugs)·D-1538-2020·2020-08-19

    Itech 361 LLC Recalls All Clean Hand Sanitizer Due to Methanol

    Itech 361 LLC is recalling 18,760 bottles of All Clean Hand Sanitizer because the product contains undeclared methanol.

    Product
    All Clean Hand Sanitizer, Fresh Scent, 1 Liter bottles, Ethyl Alcohol 70.00%, Produced by Eskbiochem SA de CV Ave Mexico Japon 50 Celaya, Gto. Mexico 38010, Distributed by All Clean Natural LTD, UPC Code 6 28055 37013 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1473-2020·2020-08-12

    Tasty Drops CBD Oil Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling Tasty Drops CBD oil due to elevated levels of undeclared lead. Consumers should stop using the product.

    Product
    Tasty Drops, Hemp Oil Extract, Spearmint, 500MG CBD, 1 FL. OZ (30ML) bottles, Dist by: Tasty Hemp Oil, Jenison, MI, UPC 6 96305 29081 1
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1450-2020·2020-08-12

    Tasty Drops Hemp Oil Extract Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling Tasty Drops Hemp Oil Extract because it contains elevated levels of undeclared lead.

    Product
    Tasty Drops Hemp Oil Extract, Vanilla, 1 FL. OZ (30ML) bottles, 300MG CBD, Dist by: Tasty Hemp Oil, Jenison, MI, UPC 8 02991 76471 4
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1455-2020·2020-08-12

    A Clean Choice CBD Tincture Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling A Clean Choice CBD tinctures due to elevated levels of undeclared lead. Consumers should stop using the product.

    Product
    A Clean Choice CBD, Hemp Oil Extract Tincture, Strawberry Creme, 1000mg, 1 fl oz (30 ml) bottles, Made in Michigan for A Clean Choice, A Division of A Clean Cigarette, Inc., 3055 Bay Rd Suite 1, Saginaw, MI 48603
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1474-2020·2020-08-12

    Tasty Drops CBD Oil Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling Tasty Drops CBD oil bottles due to elevated levels of undeclared lead. The product was sold nationwide via internet and retail channels.

    Product
    Tasty Drops, Hemp Oil Extract, Spearmint, 1000MG CBD, 1 FL. OZ (30ML) bottles, Dist by: Tasty Hemp Oil, Jenison, MI, UPC 8 02991 76539 1
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1453-2020·2020-08-12

    Hemp Extract Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling 496 bottles of Made by Hemp 1000MG Hemp Extract due to elevated levels of undeclared lead.

    Product
    Made by Hemp 1000MG Hemp Extract, Strawberry Creme, 1 OZ (30 ML) bottles, Dist by: MHR Brands, Jenison, MI, UPC 8 02991 76554 4
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1477-2020·2020-08-12

    Tasty Drops Hemp Oil Extract Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling Tasty Drops Hemp Oil Extract due to elevated levels of undeclared lead. Consumers should stop using the product.

    Product
    Tasty Drops, Hemp Oil Extract, Vanilla, 1500MG CBD,1 FL. OZ (30ML) bottles, Dist by: Tasty Hemp Oil, Jenison, MI, UPC 6 96305 29086 6
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1464-2020·2020-08-12

    Pathway To Wellness CBD Oil Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling 100 bottles of Pathway To Wellness CBD Oil due to elevated levels of undeclared lead. The product was sold nationwide via internet and retail channels.

    Product
    Pathway To Wellness, CBD Oil, Premium Hemp Oil Drops, Natural, 1000MG CBD, 1 FL OZ (30 ML) bottles, Distributed by: Pathway to Wellness
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1408-2020·2020-07-29

    Mystic Shield Hand Sanitizer Recalled for Undeclared Methanol

    Transliquid Technologies is recalling Mystic Shield hand sanitizer bottles due to the presence of undeclared methanol.

    Product
    Mystic Shield PROTECTION, ALCOHOL ANTISEPTIC 70%, Topical Solution, Antiseptic Hand Rub, Non-sterile Solution, Extra strength Formula*, 8.45 fl. oz. (250 ml) bottle, Labeled with green or blue labels, Manufactured by Mystic Intl S.A. de C.V. UPC barcode: 7 87790 33952 6
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1299-2020·2020-06-10

    Acella Recalls NP Thyroid 15 Tablets Due to Superpotent Drug Risk

    Acella Pharmaceuticals is voluntarily recalling 29,304 bottles of NP Thyroid 15 tablets because the drug is superpotent. The recall covers products distributed nationwide in the US and Puerto Rico.

    Product
    NP THYROID 15 — NP THYROID 15 (LEVOTHYROXINE, LIOTHYRONINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1300-2020·2020-06-10

    Acella Recalls Superpotent NP Thyroid 15 Thyroid Tablets Nationwide

    Acella Pharmaceuticals is voluntarily recalling 49,128 bottles of NP Thyroid 15 tablets because they are superpotent. The FDA classified this as a Class I recall.

    Product
    NP THYROID 15 — NP THYROID 15 (LEVOTHYROXINE, LIOTHYRONINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1298-2020·2020-06-10

    Acella Recalls Superpotent NP Thyroid 15 Tablets Nationwide

    Acella Pharmaceuticals is voluntarily recalling 112,140 bottles of NP Thyroid 15 tablets because the drug is superpotent. The recall covers distribution across the US and Puerto Rico.

    Product
    NP THYROID 15 — NP THYROID 15 (LEVOTHYROXINE, LIOTHYRONINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1080-2020·2020-04-08

    Natural Remedies Active Male Formula Recalled for Undeclared Tadalafil

    FDA is recalling Natural Remedies Active Male 500 mg dietary supplements because they contain undeclared Tadalafil, an FDA-approved drug for erectile dysfunction.

    Product
    Natural Remedies Active Male 500 mg Male Pleasure Formula Dietary Supplement Manufactured For: Natural Remedies San Antonio, TX, USA 1(877)543-3501
    Category
    Drug
    Distribution
    2 states
  • CriticalFDA (Drugs)·D-1036-2020·2020-03-25

    UP2 Libido Supplement Recalled for Undeclared Sildenafil

    Med Man Distribution is recalling UP2 dietary supplements because FDA analysis found undeclared sildenafil, a prescription drug, in the product.

    Product
    UP2, Dietary Supplement, All Natural Libido for Men & Women, a) one pack, b) four pack, c) ten pack capsules per carton, Exclusively Manufactured and Formulated by: Buy Wise Marketing, 4234 I-75 Business Spur, Sault Ste Marie, MI 49783, Ultimatepleasure2.com.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0867-2020·2020-02-19

    RemedyRepack Recalls Ketorolac Tromethamine Injections Due to Particulate Matter

    RemedyRepack Inc. is recalling 75 vials of Ketorolac Tromethamine 30 mg/1mL injections distributed in Oklahoma and Louisiana due to the presence of small black particles.

    Product
    Ketorolac Trom, 30 mg/1mL Inj. for I.V./I.M. Use, Rx Only, QTY: 1 ml, Repackaged by: RemedyRepack Inc., Indiana, PA 15701 NDC 70518-1239-00
    Category
    Drug
    Distribution
    2 states
  • CriticalFDA (Drugs)·D-0864-2020·2020-01-22

    Hikma Recalls Ketorolac Tromethamine Injection Due to Particulate Matter

    Hikma Pharmaceuticals is recalling specific lots of Ketorolac Tromethamine Injection because of the presence of polydimethylsiloxane particles.

    Product
    KETOROLAC TROMETHAMINE — KETOROLAC TROMETHAMINE (KETOROLAC TROMETHAMINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0656-2020·2020-01-22

    FDA Recalls Rhino 7 Platinum 30000 Capsules for Unapproved Tadafila Content

    Motto International Corp is recalling Rhino 7 Platinum 30000 Capsules because FDA analysis found the product contains tadalafil, an unapproved active ingredient.

    Product
    Rhino 7 Platinum 30000 Capsules, in blue,orange,black background with red,white,blue,gray text in hologram paper packaging, packaged in 2, 4, and 10 count blister cards, Motto International, Dallas, TX
    Category
    Drug
    Distribution
    1 state
  • CriticalFDA (Drugs)·D-0657-2020·2020-01-22

    FDA Recalls Panther Platinum 30000 Capsules for Unapproved Tadalfil Content

    Motto International Corp is recalling Panther Platinum 30000 Capsules because FDA analysis found the product contains tadalfil and was marketed without an approved NDA or ANDA.

    Product
    Panther Platinum 30000 Capsules, in green, black background with white, red text in hologram paper packaging, packaged in 2, 4, and 10 count blister cards, Motto International, Dallas, TX
    Category
    Drug
    Distribution
    1 state
  • CriticalFDA (Drugs)·D-0655-2020·2020-01-22

    FDA Recalls Unapproved Stallion Platinum 30000 Capsules Containing Tadalafil

    Motto International Corp is recalling Stallion Platinum 30000 Capsules because FDA analysis found the unapproved product contains tadalafil.

    Product
    Stallion Platinum 30000 Capsules in blue,orange,white background with red,white text in hologram paper packaging, packaged in 2, 4, 10 count blister cards, Motto International, Dallas, TX
    Category
    Drug
    Distribution
    1 state
  • CriticalFDA (Drugs)·D-0654-2020·2020-01-22

    FDA Recalls Unapproved Bull Platinum 30000 Capsules Containing Tadalafil

    Motto International Corp is recalling Bull Platinum 30000 Capsules because FDA analysis found the product contains tadalafil, a prescription drug, and it was marketed without an approved NDA or ANDA.

    Product
    Bull Platinum 30000 Capsules, 1000 mg, in orange, white, yellow background with silver text, packaged in 2, 4 and 10 count blister cards, Motto International, Dallas, TX
    Category
    Drug
    Distribution
    1 state
  • CriticalFDA (Drugs)·D-0633-2020·2020-01-08

    FDA Recalls Silver Bullet Male Enhancement Capsules for Undeclared Active Ingredient

    The FDA is recalling Silver Bullet male enhancement capsules because they contain an undeclared active ingredient (Sildenafil) and were marketed without an approved NDA/ANDA.

    Product
    Silver Bullet, Get Bigger and Harder, Works in Minutes, Lasts for Days, 10 male enhancement capsules in blister foil package, 725mg per capsule, Distributed by Silver Bullet Ltd, Golden Springs, CO, USA, UPC: 610877392698.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0351-2020·2019-11-13

    Green Lumber Natural Fuel For Men capsules recalled for undeclared Tadalafil

    Green Lumber Holdings is recalling Natural Fuel For Men capsules because FDA analysis found undeclared Tadalafil, an approved drug for erectile dysfunction.

    Product
    Green Lumber Natural Fuel For Men capsule, packaged in packs of 2, 4 and 10 capsules, 2618 San Miguel Drive, Suite #296, Newport Beach, CA 92660 (949) 426-8622.
    Category
    Drug
    Distribution
    0 states
  • CriticalFDA (Drugs)·D-0320-2020·2019-11-06

    Mero Macho Liquid Supplement Recalled for Tadalafil Contamination

    Fitoterapia USA Inc. is recalling Mero Macho Passion Fruit Vitamin C Liquid Supplement because it was marketed without an approved NDA/ANDA and found to be tainted with Tadalafil.

    Product
    Mero Macho Artificially Flavored Passion Fruit Vitamin C Liquid Supplement, 2.04 fl oz (60 mL) bottle, Manufactured By: Zaphiredelcor Cia, LTDA. Pasaje Luis Tola 9A Y Calle Juan Campuzano, Sector Carcelen, Quito-Ecuador 170302 Distributed By: Fitoterapia USA Inc., 500 NW 141 Ave.
    Category
    Drug
    Distribution
    3 states
  • CriticalFDA (Drugs)·D-0036-2020·2019-10-02

    Natpara Injection Cartridges Recalled for Potential Needle Clogging

    Shire is recalling Natpara injection cartridges because rubber stopper particles may clog the needle, potentially causing underdosing.

    Product
    Natpara (parathyroid hormone) for Injection, 50 mcg, 2 pack medication cartridges, Rx only, For subcutaneous use only, Manufactured for: Shire-NPS Pharmaceuticals, Inc., Lexington, MA NDC 68875-0203-02
    Category
    Drug
    Distribution
    0 states