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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6151–6175 of 7496

  • SevereFDA (Devices)·Z-1095-2022·2022-05-25

    Dragonfly OpStar Imaging Catheter Recall Due to Proximal Marker Separation Risk

    Abbott Vascular recalls 14,544 Dragonfly OpStar Imaging Catheters due to potential separation of the proximal marker. The affected devices were distributed throughout the US and internationally.

    Product
    Dragonfly OpStar Imaging Catheter, REF 1014651/1014652, 0.068 in, 0.014 in, 135 cm, STERILE EO
    Category
    Medical Device
    Distribution
    44 states
  • SevereFDA (Devices)·Z-1076-2022·2022-05-25

    Atrium Advanta V12 Covered Stent System Recalled for Delivery Catheter Separation

    Atrium Medical is recalling the Advanta V12 Covered Stent System worldwide for potential separation of the balloon or catheter hub during withdrawal, which may cause procedural delays and serious complications including embolism and organ infarction.

    Product
    Atrium Advanta V12 Covered Stent System (OUS only). Product Code/Part Number: 85320 85321 85322 85323 85324 85325 85326 85327 85328 85329 85330 85331 85332 85333 85334 85335 85336 85337 85338 85339 85340 85341 85342 85343 85344 85345 85350 85351 85352 85353 85354 85355 85360
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0867-2022·2022-05-25

    Milk of Magnesia USP Recalled for Microbial Contamination

    Plastikon Healthcare LLC is recalling Milk of Magnesia USP (2400 mg/30 mL) distributed in Indiana due to microbial contamination in this non-sterile product. The FDA classified this as a Class I recall.

    Product
    MILK OF MAGNESIA USP, (Magnesium Hydroxide), 2400 mg/30 mL, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Distributed by Major Pharmaceuticals, Livonia, MI 48152, NDC 0904-6846-73.
    Category
    Drug
    Distribution
    0 states
  • SevereNHTSA·22V374000·2022-05-25

    2022 Freightliner Cascadia commercial trucks recalled for brake system defect

    The 2022 Freightliner Cascadia is being recalled because a faulty valve in the air brake system can trap air and impair braking or lock the rear axle while the truck is moving.

    Product
    FREIGHTLINER — 2022 FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0868-2022·2022-05-25

    Antacid suspension product recalled due to microbial contamination

    Plastikon Healthcare LLC is recalling 23,300 antacid suspension cups due to microbial contamination. The product was distributed in Indiana for institutional use.

    Product
    Magnesium Hydroxide 1200mg, Aluminum Hydroxide 1200mg, Simethicone 120mg, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Distribute by Major Pharmaceuticals, Livonia, MI 48152, NDC: 0904-6838-73.
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Food)·F-1060-2022·2022-05-25

    Doux South Pickles Curry Cauliflower Recalled for Listeria Contamination

    Doux South Specialties LLC has recalled Bakkavor Curry Cauliflower pickles due to positive Listeria monocytogenes test results. The recall affects 145 five-gallon pails distributed to California and North Carolina.

    Product
    DOUX SOUTH PICKLES EAT WITH A SOUTHERN ACCENT BAKKAVOR CURRY CAULIFLOWER 5 GALLON
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-1069-2022·2022-05-25

    Yes! Enoki Mushrooms recalled due to Listeria monocytogenes contamination

    Yes! Enoki Mushrooms (Lot 6021053, UPC 825382736947) distributed to CA, FL, TX, and NY are being recalled because Listeria monocytogenes was detected in the product. Consumers should not consume the product and should discard it.

    Product
    Yes! Enoki Mushrooms; Pesticide Free Produce: Vacuumed packed. Product of China UPC: 825382736947 Net Wt 200g/7.05 oz Distributed by YES Produce City of Industry, CA 91746
    Category
    Food
    Distribution
    4 states
  • SevereNHTSA·22V367000·2022-05-23

    School buses recalled for steering wheels that may loosen and detach

    Navistar is recalling certain 2022-2023 IC BUS school buses. The steering wheel retaining nut may have been tightened incorrectly, allowing the steering wheel to loosen or detach. Owners should not drive their vehicles until repaired.

    Product
    IC BUS — 2023 IC BUS EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V355000·2022-05-19

    2022 International CV Vehicles Brake Sensor Fitting May Cause Brake Failure

    Navistar is recalling certain 2022 International CV vehicles because the pressure sensor fitting on the brake line assembly may not be tightened correctly, potentially causing brake fluid loss and brake failure.

    Product
    INTERNATIONAL — 2022 INTERNATIONAL CV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V354000·2022-05-19

    Hyundai Elantra and Accent seat belt pretensioners may explode in crash

    Hyundai is recalling certain 2020-2022 Accent and 2021-2022 Elantra models due to seat belt pretensioners that may explode during a crash, potentially projecting metal fragments and injuring occupants. Dealers will secure them with a cap at no charge.

    Product
    HYUNDAI — 2021 HYUNDAI ELANTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1058-2022·2022-05-18

    Valencian Almonds Recalled Due to Undeclared Peanut Contamination

    Culinary Collective is recalling Valencian Almonds due to potential peanut contamination not declared on the label. The affected products were distributed in Colorado, Montana, New York, and Oregon.

    Product
    Valencian Almonds FS Skinless, MZ502, packaged in bulk package 5 KG. Net Wt. 352 oz./22 lb. (2 bags @ 11 lb.). UPC 5 901234 123457. Ingredients: Valencian Almonds, sunflower oil, sea salt and antioxidants (mixed tocopherols and rosemary extract to preserve freshness). IMPORT
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-1057-2022·2022-05-18

    Ramen Hero vegan shoyu ramen recalled for undeclared egg allergen

    Ramen Hero is recalling certain lots of its Vegan Shoyu Ramen meal kits because they contain egg noodles despite egg not being listed on the label, posing a risk to people with egg allergies.

    Product
    Ramen Hero - Vegan Shoyu ramen (Hippie Van) Ramen noodles in a soy sauce infused vegan broth with a vegan meat ragu, roasted tomato, bell pepper and zucchini blend, and seaweed. Kits are in a frosted meal kit stand up pouch. Net Wt. 20.05 oz. (1.25 lb.) 568 g UPC: 60003
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-1045-2022·2022-05-18

    COVID-19 Antigen Test Kit Distributed Without FDA Authorization or Clearance

    The FDA is recalling 17,000 units of Joysbio SARS-CoV-2 Antigen Rapid Test Kits distributed in Alabama and Georgia. The tests were sold without FDA clearance or authorization for marketing in the United States.

    Product
    Joysbio SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold); COVID 19 Test
    Category
    Medical Device
    Distribution
    2 states
  • SevereFDA (Devices)·Z-1044-2022·2022-05-18

    COVID-19 Rapid Antigen Test Kits Recalled for Unauthorized Distribution

    Woodside Acquisitions Inc. recalled 34,240 Oral Rapid SARS-CoV-2 Antigen Test Kits distributed in Alabama and Georgia. The tests were distributed without FDA clearance or authorization for marketing.

    Product
    Oral Rapid SARS-CoV-2 Antigen Rapid Test Kit; COVID 19 Test
    Category
    Medical Device
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0856-2022·2022-05-18

    SyrSpend SF Suspending Base Recalled for Burkholderia Contamination

    Fagron is recalling SyrSpend SF Suspending Base, Cherry Flavored (NDC 51552-1123-5 and 51552-1123-9) due to contamination with Burkholderia gladioli. This FDA Class I recall affects medication used in compounding.

    Product
    SyrSpend SF Suspending Base, Cherry Flavored, packaged in a) 500mL bottles (NDC 51552-1123-5) and b) 4L bottles (NDC 51552-1123-9), Rx Only, Manufactured for Fagron, Inc., St. Paul, MN 55120.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1009-2022·2022-05-18

    FDA Recalls Accula SARS-CoV-2 Test for False Positive Risk

    Mesa Biotech is recalling approximately 6,162 units of the Accula SARS-CoV-2 Test due to an increased risk of false positive results, which could delay correct diagnosis and treatment.

    Product
    Accula SARS-CoV-2 Test, REF: COV4100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V346000·2022-05-17

    2021 Ford Expedition and Navigator: Engine Compartment Fire Risk Recall

    Ford is recalling certain 2021 Expedition and Lincoln Navigator vehicles due to risk of engine compartment fire while driving or parked. Owners should park vehicles outside away from structures until repairs are available.

    Product
    FORD — 2021 FORD EXPEDITION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V339000·2022-05-16

    2022 Freightliner Cascadia trucks recalled for disabled antilock brakes and stability control

    Daimler Trucks North America is recalling approximately 17 certain 2022 Freightliner Cascadia trucks because the antilock brakes and electronic stability control can be manually disabled, violating federal safety standards and increasing crash risk. The company will repurchase affected vehicles.

    Product
    FREIGHTLINER — 2022 FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1044-2022·2022-05-11

    TOP SAVOR Licorice Flavored Olive Recalled for Undeclared Sulfites

    A & C Best Food Trading is recalling TOP SAVOR Licorice Flavored Olive products for containing undeclared sulfites. The recalled item was distributed across 12 U.S. states.

    Product
    Olive; TOP SAVOR Licorice Flavored Olive; Net wt: 500g (17.63oz); Ingredients: olive, sugar, salt, licorice extract, food additives (citric acid, saccharin sodium, sodium benzoate, potassium sorbate), edible spices; Store in a cool and dry place. Away from direct sunlight. Distri
    Category
    Food
    Distribution
    12 states
  • CriticalFDA (Food)·F-1046-2022·2022-05-11

    Pickled Plums Recalled for Undeclared Sulfites and Prohibited Food Dye

    A & C Best Food Trading is recalling Wife Plum pickled plums in 500g jars for containing undeclared sulfites and prohibited Amaranth dye. The product poses serious health risks to sulfite-sensitive consumers.

    Product
    BEAUTIFUL AND DELICIOUS TASTE; TOP SAVOR; Wife Plum; Net wt. 500g (17.63oz); Ingredients: plum (grafting); sugar, salt, food additives (citric acid, DL malic acid, stevioside, sodium saccharine, potassium sorbate, sodium benzoate), edible spices.; Distributed by A & C best food t
    Category
    Food
    Distribution
    12 states
  • SevereFDA (Devices)·Z-0944-2022·2022-05-11

    COVID-19 Rapid Test Kits Recalled for Lacking FDA Authorization

    SML Distribution is recalling 209,450 units of Skippack COVID-19 rapid test kits that were distributed without FDA authorization or clearance. The kits were distributed nationwide across Alabama, Florida, Georgia, Missouri, New York, Texas, and Wyoming.

    Product
    Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold); COVID 19 Test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1068-2022·2022-05-11

    Salsa Texan tortillas recalled for undeclared wheat and whey allergens

    The Salsa Texan tortillas (coconut flour and blended flour varieties) are being recalled for potentially containing undeclared wheat and whey. Products were distributed online and at farmers markets.

    Product
    The Salsa Texan Coconut Flour Tortilla regular and burrito size packaged in clear flexible plastic; The Salsa Texan Blended Flour Tortilla regular and burrito size packaged in clear flexible plastic; Unlabeled tortillas sold at farmer's market in Dallas, TX area
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0877-2022·2022-05-11

    The Mandalorian Hand Sanitizer Recalled Nationwide for Benzene Contamination

    The Mandalorian Hand Sanitizer has been recalled nationwide due to FDA-detected benzene contamination. The recall affects 346,320 bottles with lot number 20E21.

    Product
    The Mandalorian Hand Sanitizer, ethyl alcohol 68%, 2.11 oz./60 mL bottles, Best Brands Consumer Products, Inc., c/o Best Brands Sales Company LLC, New York, NY NDC 74530-012-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0876-2022·2022-05-11

    Hand Sanitizer Product Recalled for Methanol Chemical Contamination

    Mickey Mouse Hand Sanitizer (ethyl alcohol 68%, 2.11 oz. bottles) is being recalled nationwide by Best Brands Consumer Products, Inc. due to methanol contamination in Lot #20D21 (expiration 06/30/2022).

    Product
    Mickey Mouse Hand Sanitizer, ethyl alcohol 68%, 2.11 oz./to mL bottle, Best Brands Consumer Products, Inc., c/o Best Brands Sales Company LLC, New York, NY NDC 74530-013-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1043-2022·2022-05-11

    Whole Foods red lentil dal recalled for possible Listeria contamination

    Whole Foods Market red lentil dal (12 oz) may contain Listeria monocytogenes. The affected product was distributed to nine states. Consumers should not consume the product.

    Product
    WHOLE FOODS MARKET red lentil dal NET WT. 12 OZ (340g) DISTRIBUTED BY: WHOLE FOODS MARKET AUSTIN, TX 78703 UPC 1 95515 02394 8
    Category
    Food
    Distribution
    9 states