The Recall Desk

Severity 5 of 5

Critical recalls

Highest-severity recall. Risk of serious injury or death is documented or strongly suspected. Stop using the product now and follow the agency's instructions.

What “critical” means here

Severity 5 (Critical) covers recalls where deaths or serious injuries have been reported, or where the agency itself classified the action as the highest severity (FDA Class I, NHTSA 'death/serious injury reported'). These are the recalls you should treat as urgent — stop using the product immediately and follow the agency's guidance. Common Severity-5 categories are pathogen-contaminated ready-to-eat foods (Listeria, E. coli O157, Salmonella), drug products with confirmed adverse-event reports, and vehicle defects with documented fatal crashes.

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.

2551–2575 of 7439

  • CriticalFDA (Food)·F-1973-2018·2018-09-26

    Market of Choice Recalls Sesame Noodle Salad Vegan for Undeclared Egg

    Market of Choice Inc is recalling Sesame Noodle Salad Vegan in 8 oz. and 16 oz. containers due to undeclared egg. The product was distributed in Oregon.

    Product
    Sesame Noodle Salad Vegan, packaged in 8 oz. or 16 oz. plastic container. UPC of 8 oz. container: 0 211630 203994. UPC of 16 oz. container: 0 211637 807492. The label is read in parts: "***SESAME NOODLE SALAD VEGAN***Soba Noodles (wheat, our, buckwheat, tapioca starch, s
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Drugs)·D-0003-2019·2018-09-26

    QuVa Pharma Recalls Subpotent Norepinephrine IV Bags Nationwide

    QuVa Pharma is recalling 528 bags of Norepinephrine 4 mg in 5% Dextrose because the active ingredient may be missing. The product was distributed to hospitals nationwide.

    Product
    Norepinephrine 4 mg (16 mcg/mL) added to 5% Dextrose 250 mL Bag Preservative Free, Rx only, QuVa Pharma, 519 Route 173, Bloombury, NJ 08804, UPC 70092103417.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1206-2018·2018-09-19

    Accord Recalls Hydrochlorothiazide Tablets Due to Product Mix-Up

    Accord Healthcare is recalling Hydrochlorothiazide 12.5 mg tablets because a customer complaint found Spironolactone 25 mg tablets in the bottles.

    Product
    HYDROCHLOROTHIAZIDE — HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·081-2018·2018-09-19

    Cargill Recalls Ground Beef Due to E. coli O26 Contamination

    Cargill Meat Solutions is recalling approximately 132,606 pounds of ground beef products that may be contaminated with E. coli O26. The recall follows an investigation linking the bacteria to 17 illnesses and one death.

    Product
    Cargill Meat Solutions — Cargill Meat Solutions Recalls Ground Beef Products due to Possible E. coli O26 Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1975-2018·2018-09-19

    Air Stream Corp. Recalls Salad Mix Due to Listeria Contamination

    Air Stream Corp. is recalling specific lots of salad mix because the product may be contaminated with Listeria monocytogenes.

    Product
    Salad Mix (Endive, Chicory, Romaine, Escarole, and Radicchio)
    Category
    Food
    Distribution
    7 states
  • CriticalFDA (Food)·F-1980-2018·2018-09-19

    Aztlan Mole Poblano Recalled for Undeclared Milk, Wheat, and Soy Allergens

    Hidroponicos Brownia is recalling Aztlan Mole Poblano because milk, wheat, and soy were not declared as ingredients or in the allergen statement.

    Product
    Aztlan Mole Poblano; 10 kg plastic buckets (22 lbs); Ingredients: sugar, Ancho pepper, peanut, soybean oil, pasilla pepper, guajillo pepper, sesame seed, cookie, cocoa, corn flour, idozided salt, condiments and spices. Sodium benzoate as a preservative. Distributed by/dis
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-0004-2019·2018-09-19

    Fuzhou Fish Balls Recalled for Undeclared Allergens

    H & C Food Inc. is recalling Fuzhou Fish Balls because they contain undeclared egg, crustacean, and pork.

    Product
    Fuzhou Fish Balls, packaged in a blue and white package bag, in two sizes: Net WT: 14 OZ (400g), UPC: 6 953640 05000 and Net WT:4.5 lbs. (2043g), UPC: 6 953640 050017. Keep Frozen.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Drugs)·D-1202-2018·2018-09-19

    HelloLife Recalls Thyroveev Homeopathic Medicine Due to Microbial Contamination

    HelloLife is recalling 370 bottles of Thyroveev homeopathic medicine due to microbial contamination. The product was distributed nationwide and internationally.

    Product
    Thyroveev, Homeopathic (OTC Medicine), 2 fl oz (59 mL) per bottle, Mftd for: HelloLife, Inc. 4635 40th St SE, Grand Rapids, MI 49512. NDC: 49726-025-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1974-2018·2018-09-19

    Air Stream Corp. Recalls Salad Mix Due to Listeria Contamination Risk

    Air Stream Corp. is recalling specific lots of salad mix because the product may be contaminated with Listeria monocytogenes.

    Product
    Salad Mix (Green Kale, Green Cabbage, Broccoli Stems, Chicory, and Brussel Sprouts)
    Category
    Food
    Distribution
    7 states
  • CriticalFDA (Drugs)·D-1200-2018·2018-09-19

    FDA Recalls Compulsin Homeopathic OTC Medicine Due to Microbial Contamination

    The FDA is recalling Compulsin Homeopathic OTC Medicine because it is contaminated with microorganisms, including Staphylococcus saprophyticus and Burkholderia cepacia.

    Product
    Compulsin, Homeopathic (OTC Medicine), 2 fl oz (59 mL) per bottle, Mftd for: HelloLife, Inc. 4635 40th St SE, Grand Rapids, MI 49512. NDC: 49726-034-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0003-2019·2018-09-19

    H & C Food Inc. Recalls Fish Balls for Undeclared Allergens

    H & C Food Inc. is recalling 14-ounce bags of fish balls because they contain undeclared egg and crustacean allergens.

    Product
    Fish Balls, packaged in a red and white plastic bag with gold font, NET WT: 14OZ (400g), UPC: 6 953006 4 50093. Keep Frozen.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Drugs)·D-1203-2018·2018-09-19

    FDA Recalls Respitrol Homeopathic Medicine Due to Microbial Contamination

    The FDA is recalling Respitrol Homeopathic OTC Medicine because it is contaminated with microorganisms, including Staphylococcus saprophyticus and Burkholderia cepacia.

    Product
    Respitrol, Homeopathic (OTC Medicine), 2 fl oz (59 mL) per bottle, Mftd for: HelloLife, Inc. 4635 40th St SE, Grand Rapids, MI 49512. NDC: 49726-003-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1201-2018·2018-09-19

    FDA Recalls Neuroveen Homeopathic OTC Medicine for Microbial Contamination

    The FDA is recalling Neuroveen Homeopathic OTC Medicine due to microbial contamination with Staphylococcus saprophyticus and Burkholderia cepacia.

    Product
    Neuroveen, Homeopathic (OTC Medicine), 2 fl oz (59 mL) per bottle, Mftd for: HelloLife, Inc. 4635 40th St SE, Grand Rapids, MI 49512. NDC: 49726-015-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·078-2018·2018-09-11

    CTI Foods Recalls Ready-to-Eat Philly Beef Steak for Listeria Risk

    CTI Foods LLC is recalling approximately 6,720 pounds of ready-to-eat Philly Beef Steak products due to possible Listeria monocytogenes contamination.

    Product
    CTI Foods LLC. — CTI Foods LLC Recalls Ready-To-Eat Philly Steak Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-1853-2018·2018-09-05

    Marsee Foods Recalls Cafe YUMM! Ginger Spice Cookies for Undeclared Peanuts

    Marsee Foods Inc is recalling Cafe YUMM! Ginger Spice Cookies because they may contain undeclared peanuts. The affected cookies were sold in Oregon and Washington.

    Product
    Ginger Spice Cookies, brand Cafe YUMM! Product is packaged in shrink wrapped master case. Each master case contains two boxes and each box contains 24 cookies. The master case is taped shut and labeled with the contents and production date, along with a lot code. The label
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Drugs)·D-0004-2019·2018-09-05

    Living Well Remedies Weight Away Remedy Recalled for Microbial Contamination

    Living Well Remedies is recalling Weight Away Remedy spray bottles due to out-of-specification microbial results.

    Product
    Living Well Remedies Weight Away Remedy, 2 fl oz (59 mL) Distributed by Living Well Remedies, LLC P.O. Box 704, Franklin Lakes, NJ 07417 www.LivingWellRemedies.com. Made in the USA
    Category
    Drug
    Distribution
    0 states
  • CriticalFDA (Food)·F-1854-2018·2018-09-05

    Marsee Foods Recalls Oatmeal Raisin Cookies for Undeclared Peanuts

    Marsee Foods is recalling Oatmeal Raisin Cookies sold at Cafe YUMM! restaurants in Oregon and Washington because they may contain undeclared peanuts.

    Product
    Oatmeal Raisin Cookies, brand Cafe YUMM! Product is packaged in shrink wrapped master case. Each master case contains two boxes and each box contains 24 cookies. The master case is taped shut and labeled with the contents and production date, along with a lot code. The lab
    Category
    Food
    Distribution
    2 states
  • CriticalUSDA FSIS·073-2018·2018-08-31

    J.T.M. Provisions Recalls Cooked Ground Beef Patties Due To Listeria

    J.T.M. Provisions is recalling approximately 960 pounds of cooked ground beef patty products due to possible Listeria monocytogenes contamination. The products were shipped to distribution centers in California.

    Product
    J T M Provisions Company — J.T.M. Provisions Company Recalls Cooked Ground Beef Products Due To Possible Listeria Contamination
    Category
    Food
    Distribution
    1 state
  • CriticalUSDA FSIS·072-2018·2018-08-30

    Publix Recalls Ground Chuck Products Due To Possible E. coli O26 Contamination

    Publix Super Markets is voluntarily recalling ground chuck products sold in Florida from June 25 to July 31, 2018, due to possible E. coli O26 contamination linked to 18 illnesses.

    Product
    Publix Supermarkets, Inc., Deli Plant — Publix Super Markets Inc. Recalls Ground Chuck Products Due To Possible E. coli O26 Contamination
    Category
    Food
    Distribution
    1 state
  • CriticalUSDA FSIS·070-2018·2018-08-29

    Taylor Farms Recalls Beef and Pork Meatloaf for Undeclared Allergens

    Taylor Farms Illinois is recalling beef and pork meatloaf products due to misbranding and undeclared eggs and wheat. No adverse reactions have been reported.

    Product
    Taylor Farms Illinois, Inc — Taylor Farms Illinois, Inc. Recalls Beef and Pork Meatloaf Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·F-1839-2018·2018-08-29

    Sherman Candy Caramels Recalled for Undeclared Tree Nuts and Peanuts

    Gift Services Inc is recalling Sherman Candy Caramels found in specific gourmet gift baskets due to undeclared pecans, walnuts, almonds, and/or peanuts.

    Product
    Sherman Candy Caramels are individually wrapped in plastic and then sealed in a cardboard flexible carton. Each Sherman Candy Caramels contains 3 pieces inside and sold in the following gift baskets: Metropolitan Gourmet Gift Basket. Encore Gourmet Gift Basket. Toast of C
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1832-2018·2018-08-29

    HP Hood Recalls Blue Diamond Almond Milk Due to Milk Allergen

    HP Hood LLC is recalling Blue Diamond Almond Breeze Almond Milk, Half Gallon, because the product tested positive for milk allergen.

    Product
    Blue Diamond Almond Breeze Almond Milk, Half Gallon
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Drugs)·D-1179-2018·2018-08-29

    FDA Recalls Levothyroxine and Liothyronine Tablets Due to Content Uniformity Failures

    Westminster Pharmaceuticals is recalling Levothyroxine and Liothyronine tablets because they failed content uniformity specifications due to an adulterated ingredient and poor manufacturing controls.

    Product
    Levothyroxine and Liothyronine (Thyroid Tablets, USP), 1 & 1/2 grain (90 mg), 100-count bottles, Rx Only, Manufactured for: Westminster Pharmaceuticals, LLC, 154 Downing Street, Unit 1 & 2, Olive Branch, MS 38654, NDC 69367-157-04.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1182-2018·2018-08-29

    FDA Recalls Levothyroxine and Liothyronine Thyroid Tablets Due to Content Uniformity Failures

    Westminster Pharmaceuticals is recalling Levothyroxine and Liothyronine tablets because they failed content uniformity specifications, potentially resulting in incorrect drug strength.

    Product
    Levothyroxine and Liothyronine (Thyroid Tablets, USP), 2 grain (120 mg), 100-count bottles, Rx Only, Manufactured for: Westminster Pharmaceuticals, LLC, 154 Downing Street, Unit 1 & 2, Olive Branch, MS 38654, NDC 69367-158-04.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1181-2018·2018-08-29

    FDA Recalls Levothyroxine and Liothyronine Tablets Due to Content Uniformity Failures

    Westminster Pharmaceuticals is recalling Levothyroxine and Liothyronine tablets because they failed content uniformity specifications due to an adulterated ingredient and poor manufacturing controls.

    Product
    Levothyroxine and Liothyronine (Thyroid Tablets, USP), 1/4 grain (15 mg), 100-count bottles, Rx Only, Manufactured for: Westminster Pharmaceuticals, LLC, 154 Downing Street, Unit 1 & 2, Olive Branch, MS 38654, NDC 69367-159-04.
    Category
    Drug
    Distribution
    Distributed nationwide