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.

20326–20350 of 32117

  • SevereUSDA FSIS·032-2016·2016-04-29

    Greencore USA Recalls Meat and Poultry Products Produced Without Inspection

    Greencore USA is recalling approximately 1,341 pounds of meat and poultry wraps and salads produced without federal inspection. No adverse reactions have been reported.

    Product
    Greencore USA Recalls Meat, Poultry Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    7 states
  • SevereUSDA FSIS·033-2016·2016-04-29

    Foster Farms Recalls Frozen Chicken Nuggets Due to Foreign Materials

    Foster Farms is recalling approximately 220,450 pounds of frozen chicken nuggets that may contain blue plastic and black rubber.

    Product
    Case Farms, Processing — Foster Poultry Farms Recalls Poultry Products Due To Possible Foreign Materials Contamination
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·16V260000·2016-04-29

    Thor Motor Coach Recalls 2017 ACE and Road Bear Rental Motorhomes

    Thor Motor Coach is recalling 2017 ACE and Road Bear Rental motorhomes because seat belt anchorages in the slide-out section may pull loose during a crash.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH ROAD BEAR RENTAL, ACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V261000·2016-04-29

    Mercedes-Benz and Freightliner Sprinter Vans Recalled for Window Separation Risk

    Daimler Vans USA is recalling 2015-2016 Mercedes-Benz and Freightliner Sprinter vans because multiple paint layers may cause windows to separate in a crash.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 2500, SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V252000·2016-04-28

    Newmar Recalls 2014-2016 Motorhomes Due to Brake Signal Defect

    Newmar is recalling 1,150 recreational vehicles because the brake signal to towed devices may not deactivate, causing dragging brakes, overheating, or fire.

    Product
    NEWMAR — NEWMAR LONDON AIRE, ESSEX, MOUNTAIN AIRE, DUTCH STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V256000·2016-04-28

    GM Recalls 2016-2017 Trucks and SUVs for Front Control Arm Weld Defect

    General Motors is recalling specific 2016-2017 Chevrolet, GMC, and Cadillac vehicles because inadequate welds on the front upper control arms may separate, compromising steering and increasing crash risk.

    Product
    CHEVROLET — CHEVROLET, GMC, CADILLAC SILVERADO 1500, SIERRA 1500, TAHOE, YUKON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1097-2016·2016-04-27

    Chicago Kimchee Recalls Korea White Kimchee for Undeclared Anchovies

    Chicago Kimchee is recalling Korea white Kimchee because it contains undeclared anchovies. Consumers with this product should stop using it.

    Product
    Korea white Kimchee packaged in 1 gallon, 1/2 gallon, packaged in glass jars inside plastic containers with multi colored label and black lettering.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0825-2016·2016-04-27

    Impax Recalls Dextroamphetamine Sulfate Tablets Due to Failed Impurity Specifications

    Impax Laboratories is recalling 67,428 bottles of Dextroamphetamine Sulfate Tablets USP, 10 mg, because the product failed impurities and degradation specifications.

    Product
    Dextroamphetamine Sulfate Tablets USP, 10 mg, 100-count bottle, Rx only, Manufactured and Distributed by: Corepharma, LLC, Middlesex, NJ 08846, NDC 64720-0216-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V248000·2016-04-27

    Ford Recalls 2011-2012 F-150, Mustang, Expedition, Navigator for Transmission Defect

    Ford is recalling specific 2011-2012 F-150, Mustang, Expedition, and Navigator vehicles because the automatic transmission may unexpectedly downshift to first gear, increasing crash risk.

    Product
    FORD — FORD, LINCOLN F-150, MUSTANG, EXPEDITION, NAVIGATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1124-2016·2016-04-27

    Native Catch Salmon Bacon Recalled for Potential Botulism Risk

    Swinomish Fish Company is recalling Native Catch Salmon Bacon, Peppered flavor, due to potential Clostridium botulinum contamination discovered during a routine inspection.

    Product
    Native Catch Salmon Bacon, Peppered flavor. UPC: 7 51778 15900 0. Peppered Salmon Bacon is ground and seasoned skinless/boneless salmon, extruded, peppered, smoked, cooled and vacuum packed in 8 oz., 14 oz. and 5 lbs. clear vacuum bags. Label states keep refrigerated or…
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-1342-2016·2016-04-27

    Boston Scientific Recalls Fetch 2 Aspiration Catheters Due to Shaft Breaks

    Boston Scientific is recalling Fetch 2 Aspiration Catheters because the catheter shafts may break, potentially requiring additional procedures to remove the broken piece from patients.

    Product
    Boston Scientific Fetch 2 Aspiration Catheter, Catalog No. 109400-001. Product The Fetch 2 Aspiration Catheter is indicated for the removal of fresh, soft emboli and thrombi from vessels in the peripheral and coronary vasculature.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1096-2016·2016-04-27

    Chicago Kimchee Recalls Kimchee for Undeclared Anchovies

    Chicago Kimchee is recalling chopped Kimchee products due to undeclared anchovies, a major food allergen.

    Product
    Korea chopped Kimchee packaged in 1 gallon, 1/2 gallon, 1/4 gallon, and 1/8 gallon packaged in glass jars inside plastic containers with multi colored label and black lettering.
    Category
    Food
    Distribution
    0 states
  • SevereNHTSA·16V249000·2016-04-27

    2016 Jeep Grand Cherokee Recall for Brake Shift Interlock Defect

    Chrysler is recalling 2016 Jeep Grand Cherokee vehicles because a loose electrical connection in the brake transmission shift interlock solenoid may cause the transmission to lock in Park or Neutral.

    Product
    JEEP — JEEP GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1123-2016·2016-04-27

    Native Catch Salmon Bacon Recalled for Potential Botulism Contamination

    Swinomish Fish Company is recalling Native Catch Salmon Bacon due to potential Clostridium botulinum contamination discovered during a routine inspection.

    Product
    Native Catch Salmon Bacon, Traditional flavor. UPC 7 83583 27965 9. Traditional Salmon Bacon is ground and seasoned skinless/boneless salmon, extruded, peppered, smoked, cooled and vacuum packed in 8 oz., 14 oz., and 5 lbs. clear vacuum bags. Label states keep…
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1088-2016·2016-04-27

    Bimbo and Sara Lee Whole Wheat Bread Recalled for Glass Contamination

    BIMBO Bakeries USA Inc. is recalling multiple brands of 100% Whole Wheat Bread due to possible glass contamination. Consumers should check their bread bags for the specific UPCs and dates listed.

    Product
    Bimbo 100% Whole Wheat Bread, 16oz, On bag: SEP 01, UPC: 7432309230 Sara Lee 100% Whole Wheat Bread 16 oz On bag: SEP 01 UPC: 7294561103; Sara Lee 100% Whole Wheat Bread 20 oz On bag: SEP 01 UPC: 7294560134; Kroger 100% Whole Wheat Round Top Bread, 16 oz, On…
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Devices)·Z-1551-2016·2016-04-27

    Smith & Nephew Recalls TC-PLUS Knee Prosthesis Due to Dimensional Deviation

    Smith & Nephew is recalling 6 units of TC-PLUS tibial knee prostheses due to a dimensional deviation that may prevent the polyethylene insert from seating correctly during surgery.

    Product
    TC-PLUS(TM), Primary Fixed Tibial Component VKS Right, SIZE 12 RIGHT, STERILE R, REF 12 000 028, S&N 7500283, Smith & Nephew Orthopaedics AG Product Usage: Tibial knee prosthesis
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0832-2016·2016-04-27

    Hospira Recalls Potassium Chloride Injection Bags Due to Chemical Contamination

    Hospira Inc. is recalling 81,888 bags of Potassium Chloride Injection due to potential contamination with an aromatic hydrocarbon resin.

    Product
    Potassium Chloride Injection 20 mEq, 400 mEq/L, Packaged in 50 mL Bags, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7077-14
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1082-2016·2016-04-27

    Brian's Cauliflower Recalled for Undeclared Sulfites

    European Natural Foods & Trading Company is recalling Brian's Cauliflower 83 oz jars due to undeclared sulfites. The product was distributed in Connecticut, Massachusetts, New Jersey, and New York.

    Product
    Brians Cauliflower 83 oz Imported by EUROPEAN NATURAL FOOD & TRADING CO. Inc, 72 Lehigh Avenue Paterson, NJ 07593 UPC 858567002421
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-1530-2016·2016-04-27

    Acorn 180 Curved Stairlift Recalled Due to Broken Rivets

    Acorn Stairlifts Inc is recalling 1,290 Acorn 180 Curved Stairlifts in the US because aluminum rivets may break under prolonged use.

    Product
    Acorn 180 Curved Stairlift
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1092-2016·2016-04-27

    Peru Food Mote Corn Recalled for Undeclared Sulfites

    Peru Food Import Inc. is recalling 2,664 bags of Mote Corn Maiz Mote due to undeclared sulfites. The product was distributed in New York and Connecticut.

    Product
    Peru Food Mote Corn Maiz Mote Net Wt. 15 oz. Imported and distributed by: Peru Food Import Inc.PO Box 419 West New York, NJ 07093 UPC 812125009628
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-1090-2016·2016-04-27

    Brett Anthony Foods Recalls Wild Mushroom Soup for Undeclared Chestnuts

    Brett Anthony Foods is recalling 24 oz containers of Wild Mushroom Soup because the product is mislabeled and does not declare chestnuts.

    Product
    Wild Mushroom Soup packaged in a 24 oz clear plastic container with green and white label and green lettering.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0828-2016·2016-04-27

    Hospira Recalls Dextrose Injection Bags Due to Chemical Contamination

    Hospira Inc. is recalling 4,368 bags of Dextrose Injection, USP, 50% due to potential contamination with an aromatic hydrocarbon resin.

    Product
    Dextrose Injection, USP, 50%, Packaged as 500 mL in 1000 mL Bag, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7936-19, Barcode (01) 0 030409 793619 9
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0829-2016·2016-04-27

    Hospira Recalls Dextrose Injection Bags Due to Chemical Contamination Risk

    Hospira Inc. is recalling 552 bags of Dextrose Injection, USP, 20% due to potential contamination with an aromatic hydrocarbon resin.

    Product
    Dextrose Injection, USP, 20%, Packaged as 500 mL in 1000 mL Bags, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7935-19, Barcode (01) 0 030409 793519 2
    Category
    Drug
    Distribution
    Distributed nationwide