The Recall Desk

Severity 4 of 5

Severe recalls

The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.

What “severe” means here

Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.

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.

25776–25800 of 32215

  • SevereFDA (Food)·F-1744-2014·2014-04-09

    Net Food Turkey Dried Apricots Recalled for Undeclared Sulfites

    Net Food Import and Export LLC is recalling Turkey Dried Apricots because NYSDAM analysis found undeclared sulfites. The product was distributed in New Jersey.

    Product
    Net Food Turkey Dried Apricots Net Weight 16.1 oz (454 g) Thunderbolt Export & Imports 743 Fairview Avenue. Suit :2 Arcadia, CA 91007 USA UPC 8697445250019
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1724-2014·2014-04-09

    Fresh To Go Tuscan Style Sandwiches Recalled for Undeclared Pine Nuts

    H.C. Schau & Son is recalling Fresh To Go Tuscan Style Combo sandwiches because they contain undeclared pine nuts, a tree nut allergen.

    Product
    8 oz. Tuscan Style Combo on Tomato Basil Spread sandwiches individually wrapped in clear plastic wrap sold under the Fresh To Go brand.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1713-2014·2014-04-09

    Roos Foods Recalls Queso Fresco Due to Listeria Monocytogenes Contamination

    Roos Foods Inc. is recalling Amigo Brand Queso Fresco because samples of related cheese products tested positive for Listeria Monocytogenes.

    Product
    Queso Fresco Amigo Brand Round Fresh Cheese, 16 oz. wrapped in cellophane, Manufactured by: Roos Foods, Inc. Kenton, DE 19955, Plant No. 10-5436, UPC code 095548003316. (Ingredients: Pasteurized whole milk, salt, rennet, calcium, lactic acid).
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-1704-2014·2014-04-09

    Mrs. Griffin's Barbecue Sauce Recalled for Undeclared Milk Allergen

    Bar-Jim Inc. is recalling Mrs. Griffin's Original Barbecue Sauce because it contains undeclared milk, a major food allergen.

    Product
    Mrs. Griffin's Original Barbecue Sauce, Net 32 Fl.oz. (946 mL), Made by Griffin Barbecue Sauce, Inc., Macon GA 31206
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1719-2014·2014-04-09

    Roos Foods Recalls Santa Rosa de Lima Sour Cream Due to Listeria

    Roos Foods is recalling Santa Rosa de Lima sour cream products because Listeria monocytogenes was found in samples of fresh curd cheese from the same facility.

    Product
    Santa Rosa de Lima Crema Salvadorena Cultured Sour Cream, 80 oz. (5lbs), packaged in a Plastic Tub, Roos Foods, Inc., Kenton, DE 19955, Plant No. 10-5436, UPC code 095548003934. Santa Rosa de Lima Crema Salvadorena Culture Sour Cream, Grade A, 16 oz., packed in a plastic jar…
    Category
    Food
    Distribution
    6 states
  • SevereNHTSA·14V169000·2014-04-09

    Toyota Recalls Yaris and Scion xD for Seat Rail Spring Defect

    Toyota is recalling 2006-2010 Yaris and 2008-2010 Scion xD vehicles because seat rail springs may break, potentially allowing the seat to move during a crash.

    Product
    TOYOTA — TOYOTA, SCION YARIS, XD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1320-2014·2014-04-09

    Merit Medical Systems Recalls Non-Sterile Custom Syringe Kits

    Merit Medical Systems is recalling 15 syringe kits labeled as sterile but not sterilized. The products were distributed in the US, Thailand, and Hong Kong.

    Product
    Merit Custom Syringe Kit, Convenience Kit, I.R. Embolization Pack, K02-01010A, Sterile EO.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1703-2014·2014-04-09

    Mrs. Griffin's Hot Barbecue Sauce Recalled for Undeclared Milk Allergen

    Bar-Jim Inc. is recalling Mrs. Griffin's Hot Barbecue Sauce because it contains undeclared milk, a major food allergen.

    Product
    Mrs. Griffin's Hot Barbecue Sauce, Net 1 Gallon (13.785L), Made by Griffin Barbecue Sauce, Inc., Macon GA 31206
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1743-2014·2014-04-09

    Whole Foods Tom Yom Soup Recalled for Undeclared Milk Allergen

    Whole Foods Market is recalling Tom Yom Soup because the ingredient list includes whey but fails to declare milk as the source of the allergen.

    Product
    Tom Yom Soup, 24 oz. plastic cups, packed 6 cups\cardboard case, and labeled in part ***Manufactured by Whole Foods Market, Landover, MD 20785***UPC 00000601467***
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Devices)·Z-1298-2014·2014-04-09

    Draeger PS500 Power Supply Unit Recalled Due to Reduced Battery Capacity

    Draeger Medical Systems is recalling 1,544 PS500 Power Supply Units because the battery capacity did not last as long as expected.

    Product
    Draeger PS500 Power Supply Unit of the Infinity ACS Workstation Critical Care (Evita Infinity V500), Evita V500 and /or Babylog VN500 Ventilators, used for ventilation during short term transport of patients within a hospital.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1725-2014·2014-04-09

    Unilever Recalls Popsicle Ice Pops Due to Potential Milk Exposure

    Unilever is voluntarily recalling specific Popsicle ice pop boxes because they may have been exposed to milk, an ingredient not listed on the label.

    Product
    Popsicle Orange Cherry Grape 20 pops Net 33 fl oz Unilever Englewood Cliffs, NJ 07632 USA UPC 077567121301
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1727-2014·2014-04-09

    Winn-Dixie Chocolate Drink Mix Recalled for Undeclared Milk Allergen

    Winn-Dixie is recalling Chocolate Flavored Drink Mix because it may contain an undeclared milk allergen. The product was distributed in Florida.

    Product
    Winn-Dixie Chocolate Flavored Drink Mix NET WT 30 OZ (1 LB 14 OZ) 851 G Distributed by: Winn-Dixie Stores, Jacksonville, FL 32254
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1308-2014·2014-04-09

    RaySearch Ray Station 4.0 software recalled for dose calculation errors

    RaySearch Laboratories is recalling Ray Station 4.0 software due to clinical dose calculation errors during radiation therapy.

    Product
    RaySearch Ray Station, Radiation Therapy Treatment Planning System, Stand-alone software
    Category
    Medical Device
    Distribution
    7 states
  • SevereNHTSA·14V179000·2014-04-09

    Winnebago Recalls 2014-2015 Motorhomes for Brake Hose Defect

    Winnebago is recalling specific 2014-2015 motorhomes because a manufacturing defect may have damaged brake hoses, potentially causing fluid leakage and reduced braking performance.

    Product
    WINNEBAGO — WINNEBAGO TRAVATO, ITASCA VIVA, TREND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1705-2014·2014-04-09

    Mrs. Griffin's Barbecue Sauce Recalled for Undeclared Milk Allergen

    Bar-Jim Inc. is recalling Mrs. Griffin's Hickory Smoke Barbecue Sauce because it contains undeclared milk, a major food allergen.

    Product
    Mrs. Griffin's Hickory Smoke Barbecue Sauce, Net 32 Fl.oz. (946 mL), Made by Griffin Barbecue Sauce, Inc., Macon GA 31206
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1722-2014·2014-04-09

    Roos Foods Recalls Santa Rosa de Lima Cheese Due to Listeria

    Roos Foods is recalling Santa Rosa de Lima cheese products after samples tested positive for Listeria monocytogenes. The recall includes all brands, lots, and sizes from the facility.

    Product
    Santa Rosa de Lima Mantequilla de Bolsa Tradicion Centroamericana, 15 oz., packaged in a plastic bag, Manufactured by Roos Foods, Inc., UPC code 095548002159. (Ingredients: Cream, milk, water, salt, nonfat dry milk, cultured skim powder, gelatin, stabilizers (carrageean gum…
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-1723-2014·2014-04-09

    Roos Foods Recalls La Chapina Cream Due to Listeria Contamination

    Roos Foods Inc is recalling La Chapina Crema Guatemalteca because samples of a related cheese product tested positive for Listeria monocytogenes.

    Product
    La Chapina Crema Guatemalteca Guatemalan Style Cream, 16 oz. packaged in a plastic bag, Distribuido por: Roos Foods Distributors, 645 Lofstrand Lane, Rockville, MD 20850, UPC code 095548000414. (Ingredients: Cream, milk, water, salt, nonfat dry milk, cultured skim milk powder…
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-1721-2014·2014-04-09

    Roos Foods Recalls Amigo Brand Sour Cream Due to Listeria Contamination

    Roos Foods is recalling Amigo Brand Crema Centroamericana Cultured Sour Cream because Listeria monocytogenes was found in samples of cheese from the same facility.

    Product
    Amigo Brand Crema Centroamericana Cultured Sour Cream, Grade A, 16 oz., packed in a plastic jar, Roos Foods, Inc., Kenton, DE 19955, Plant No. 10-5436, UPC code 09554800079. (Ingredients: Cream, milk, salt, nonfat dry milk, skim milk powder, gelatin, stabilizers (carrageean…
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Devices)·Z-1311-2014·2014-04-09

    Zoll Medical Defibrillators Recalled for Continuous Device Reset Loop

    Zoll Medical is recalling 3,169 defibrillator/pacemaker/monitor units because they may latch in a continuous reset loop, rendering them unusable.

    Product
    Zoll Medical X Series, PropaqMD, PropaqM Defibrillator/Pacemaker/Monitor With System Software Version 02.10.02.00 or Higher, automated external defibrillator.
    Category
    Medical Device
    Distribution
    Distributed nationwide