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 the agency’s own highest classification or reported deaths or serious injuries, 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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2376–2400 of 7451

  • CriticalFDA (Drugs)·D-0388-2019·2019-01-30

    5K Premium Enhancement capsules recalled for undeclared sildenafil and tadalafil

    Happy Together, Inc. is recalling 5K Premium Enhancement capsules because FDA analysis found undeclared sildenafil and tadalafil.

    Product
    5K Premium Enhancement capsule, 5000 mg, 1 count blister card, box of 30, Happy Together Inc., Boynton, FL UPC 649964965644
    Category
    Drug
    Distribution
    0 states
  • CriticalFDA (Devices)·Z-0737-2019·2019-01-30

    Draeger Medical Recalls VentStar Basic 250 Breathing Circuits Due to Assembly Error

    Draeger Medical is recalling 170 units of VentStar Basic 250 breathing circuits because they were incorrectly pre-assembled, creating a risk of incorrect connection or short circuiting.

    Product
    VentStar Basic 250, Catalog Number MP00350 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only. Breathing Circuits/Anesthesia Sets…
    Category
    Medical Device
    Distribution
    12 states
  • CriticalUSDA FSIS·008-2019·2019-01-28

    Perdue Recalls Chicken Nuggets Due to Undeclared Milk Allergen

    Perdue Foods is recalling refrigerated chicken nuggets because they contain milk, a known allergen, that is not listed on the label.

    Product
    PERDUE FOODS, LLC. — Perdue Foods, LLC Recalls Refrigerated Fun Shapes Chicken Breast Nuggets Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    14 states
  • CriticalUSDA FSIS·007-2019·2019-01-25

    Harvest Food Group Recalls Chicken Fried Rice for Undeclared Milk Allergen

    Harvest Food Group is recalling 47,332 pounds of chicken fried rice products because they contain milk, a known allergen, that is not declared on the label.

    Product
    Harvest Food Group, LLC — Harvest Food Group, Inc. Recalls Poultry Products Due to Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    2 states
  • CriticalUSDA FSIS·005-2019·2019-01-18

    Custom Made Meals Recalls Chicken Skewers Due to Undeclared Coconut Allergen

    Custom Made Meals, LLC is recalling Red Chili Orange Chicken Skewers because they contain coconut, a tree nut allergen not listed on the label.

    Product
    Custom Made Meals, LLC — Custom Made Meals, LLC Recalls Chicken Skewer Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Drugs)·D-0372-2019·2019-01-16

    Sun Pharmaceutical Recalls Vecuronium Bromide Due to Glass Particulates

    Sun Pharmaceutical Industries is recalling Vecuronium Bromide for Injection because glass particles were detected in the product.

    Product
    VECURONIUM BROMIDE — VECURONIUM BROMIDE (VECURONIUM BROMIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0358-2019·2019-01-16

    Lupin Recalls Ceftriaxone Injection Vials Due to Rubber Particulate Matter

    Lupin Pharmaceuticals is recalling Ceftriaxone for Injection USP due to the presence of grey rubber particulate matter in the vials.

    Product
    Ceftriaxone for Injection USP, 2 g, packaged in 10 Single Use Vials (NDC 68180-644-01) per box, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., 111 South Calvert Street, Baltimore, Maryland 21202; Manufactured by: Lupin Limited, Mandideep 462 046 INDIA, NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalNHTSA·19V008000·2019-01-09

    Subaru Recalls Vehicles Due to Passenger Air Bag Inflator Explosion Risk

    Subaru is recalling specific 2010-2014 models because passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.

    Product
    SUBARU — SUBARU FORESTER, IMPREZA, OUTBACK, LEGACY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·19V010000·2019-01-09

    Mercedes-Benz Recalls Vehicles Due to Passenger Air Bag Inflator Defect

    Mercedes-Benz is recalling specific 2010-2017 models because passenger air bag inflators may explode due to humidity, posing a risk of serious injury or death.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES BENZ C300, E350, GLK350, C350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0552-2019·2019-01-09

    Medtronic StealthStation Cranial Software Recall for Biopsy Depth Gauge Error

    Medtronic is recalling StealthStation Cranial and Synergy Cranial software due to an incorrect display of the Biopsy Depth Gauge that resulted in the biopsy of healthy tissue.

    Product
    StealthStation Cranial and Synergy Cranial Depth Gauge: StealthStation Cranial Optical Pocket Guide - Instructions for cranial procedures using optical localization StealthStation Cranial version 3.0, 3.1 CE 0344 Rx Only 2018-02 9735489 Revision 3 Medtronic Navigation, Inc.…
    Category
    Medical Device
    Distribution
    51 states
  • CriticalFDA (Drugs)·D-0347-2019·2019-01-02

    Phenylephrine HCl Injectable Solution Recalled for Incorrect Concentration Labeling

    Advanced Pharma Inc. is recalling 225 syringes of Phenylephrine HCl injectable solution because the label incorrectly states the concentration as 10 mcg per mL instead of 100 mcg per mL.

    Product
    Phenylephrine HCl, 1 mg in Sterile Water for Injection, QS 10mL Injectable Solution, 1 mg/10 mL incorrectly labeled as (10 mcg per mL), 10 mL syringe, Rx only, Avella of Houston, 9265 Kirby Dr., Houston, TX 77054, (877) 794-0404; NDC: 42852-802-61.
    Category
    Drug
    Distribution
    3 states
  • CriticalFDA (Food)·F-0820-2019·2019-01-02

    Apio Recalls Eat Smart Salad Shake Ups Due to Listeria

    Apio, Inc. is recalling specific varieties of Eat Smart Salad Shake Ups after the Canadian Food Inspection Agency detected Listeria monocytogenes.

    Product
    Eat Smart Salad Shake Ups - Raspberry Acai/Framboises ET: 5.5 oz. (156 g); US UPC 7 09351-30178 0; Canadian UPC: 7 09351 30196 4. Product of USA Distributed by Apio Inc., Guadalupe, Ca 93434
    Category
    Food
    Distribution
    14 states
  • CriticalNHTSA·19E003000·2019-01-02

    Takata Frontal Passenger Air Bag Inflator Recall for 2010+ Vehicles

    Takata is recalling specific frontal passenger air bag inflators in 2010 or newer vehicles registered in 22 states due to a risk of explosion.

    Product
    AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0821-2019·2019-01-02

    Apio Recalls Eat Smart Salad Shake Ups Due to Listeria

    Apio, Inc. is recalling Eat Smart Salad Shake Ups after the Canadian Food Inspection Agency detected Listeria monocytogenes in the product.

    Product
    Eat Smart Salad Shake Ups - Sweet Kale/Chou Frise Doux: 5.5 oz. (156 g); US UPC 7 09351-30240 4; Canadian UPC: 7 09351 30243 5. Product of USA Distributed by Apio Inc., Guadalupe, Ca 93434
    Category
    Food
    Distribution
    14 states
  • CriticalFDA (Food)·F-0819-2019·2019-01-02

    Apio Recalls Eat Smart Salad Shake Ups Due to Listeria Risk

    Apio, Inc. is recalling Eat Smart Salad Shake Ups in Avocado Ranch flavor because the Canadian Food Inspection Agency detected Listeria monocytogenes in the product.

    Product
    Eat Smart Salad Shake Ups - Avocado Ranch/Ranch et Avocats: 5.5 oz. (156 g); US UPC: 7 09351-30177 3; Canadian UPC: 7 09351 30195 7; Product of USA Distributed by Apio Inc., Guadalupe, Ca 93434
    Category
    Food
    Distribution
    14 states
  • CriticalFDA (Food)·F-0818-2019·2019-01-02

    Apio Recalls Eat Smart Salad Shake Ups Due to Listeria

    Apio, Inc. is recalling specific varieties of Eat Smart Salad Shake Ups after the Canadian Food Inspection Agency detected Listeria monocytogenes.

    Product
    Eat Smart Salad Shake Ups - Asian Sesame/Sesame Asiatique; 5.5 oz. (156 g); UPC 7 09351-30241 1, 7 09351 30244 2 Product of USA Distributed by Apio Inc., Guadalupe, Ca 93434
    Category
    Food
    Distribution
    14 states
  • CriticalFDA (Food)·F-0730-2019·2018-12-26

    Achdut Recalls Tahini Products Due to Potential Salmonella Contamination

    Achdut is recalling specific Baron's and Galil tahini products because they may be contaminated with Salmonella. The products were distributed in New York, California, Pennsylvania, and Israel.

    Product
    Tahini sold under the following brand names: Baron's Tahini double pack, 454g, UPC: X000EZ2HCB; Galil whole tahini, 500g, UPC: 814968020037
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0775-2019·2018-12-26

    Inspired Organic Sunflower Butter Recalled for Listeria monocytogenes Contamination

    Lipari Foods is recalling Inspired Organic Sunflower Butter because product testing found Listeria monocytogenes. The recall covers 972 cases distributed across 15 states and Canada.

    Product
    Inspired Organic Sunflower Butter 16oz. plastic jar, 6 per case UPC #: 863669742526 refrigerate after opening
    Category
    Food
    Distribution
    15 states
  • CriticalFDA (Food)·F-0733-2019·2018-12-26

    Sprout Creek Farm Raw Cows' Milk Cheese Recalled for Listeria Risk

    Sprout Creek Farm is recalling four wheels of Kinkead raw cows' milk cheese due to potential Listeria monocytogenes contamination.

    Product
    Sprout Creek Farm Kinkead raw cows' milk cheese semi-firm savory brothy. The product is packaged with an orange label.
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Drugs)·D-0360-2019·2018-12-26

    Lubrisine eye drops recalled for undeclared colloidal silver and sterility issues

    Results RNA, LLC is recalling Lubrisine eye drops nationwide due to lack of sterility assurance and the presence of undeclared colloidal silver.

    Product
    Lubrisine eye drops (polyethylene glycol 400 0.4% and Propylene glycol 0.3%), 30 ML bottle, Manufactured and Distributed by: Results RNA, LLC, 1272 S 1380 W., Orem, UT 84058, UPC 7 9238230723 4
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0748-2019·2018-12-26

    Bakkavor Baked Macaroni and Cheese Recalled for Undeclared Allergens

    Bakkavor Foods USA Inc. is recalling Baked Macaroni and Cheese because it contains lobster, shrimp, and soy that are not listed on the label.

    Product
    Baked Macaroni and Cheese, NET WT 12 OZ (340g), CONTAINS: WHEAT, MILK, EGG, Produced By BAKKAVOR USA, 2700 Westinghouse Blvd. Charlotte, NC 28273, Phone: 704-522-1977, UPC 7 61088 80502 3
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0776-2019·2018-12-26

    Lipari Foods Recalls Inspired Organic Almond Butter Due to Listeria

    Lipari Foods is recalling Inspired Organic Almond Butter because product testing found Listeria monocytogenes. Consumers should stop using the product.

    Product
    Inspired Organic Almond Butter 16oz. plastic jar, 6 per case UPC #: 863669742540 refrigerate after opening
    Category
    Food
    Distribution
    15 states
  • CriticalFDA (Food)·F-0729-2019·2018-12-26

    Galil Seasoned Tahini Recalled Due to Salmonella Contamination Risk

    Achdut is recalling Galil Seasoned Tahini because it may be contaminated with Salmonella. The product was distributed in New York, California, Pennsylvania, and Israel.

    Product
    Seasoned Tahini sold under the following brand name: Galil Seasoned Tahini, 500g, UPC: 814968020020
    Category
    Food
    Distribution
    3 states