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.

17751–17775 of 29217

  • SevereNHTSA·16V646000·2016-09-07

    Audi Recalls 2012-2013 A6 and A7 for Fuel Hose Leak Risk

    Volkswagen Group of America is recalling 28,249 Audi A6 and A7 vehicles because a fuel hose may degrade and leak, increasing fire risk.

    Product
    AUDI — AUDI A6, A7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1997-2016·2016-09-07

    Sanwa Organic Hot Finger Peppers Recalled for Salmonella Contamination

    Sanwa International Wholesale Foods is recalling Organic Hot Finger Peppers sold in Florida due to a positive test for Salmonella.

    Product
    Organic Hot Finger Peppers (Florida), sold in 0.5-1 lb plastic bags. Each case will hold approximately 15-20 bags.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-2023-2016·2016-09-07

    Awrey's Bakery Recalls Chocolate Roll Cakes Due to Undeclared Walnuts

    Minnie Marie Bakers, Inc. dba Awrey's Bakery is recalling Chocolate Roll Cakes in Ohio because they may contain undeclared walnuts, posing a risk to people with tree nut allergies.

    Product
    Chocolate Roll Cake 15x24 22 lb case 8, 2 lb 12 oz cakes per case
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2676-2016·2016-09-07

    Intuitive Surgical Recalls da Vinci EndoWrist Stapler 30 Instruments

    Intuitive Surgical is recalling 875 da Vinci EndoWrist Stapler 30 instruments due to reported field failures involving shaft rotation interruption or jaws not opening.

    Product
    STAPLER 30,IS4000; Model number 470430; General and Plastic Surgery: The Intuitive Surgical da Vinci EndoWrist Stapler 30 Instrument and Stapler 30 Reloads are intended to be used with the da Vinci Xi Surgical System (Model IS4000) for resection, transection and/or creation…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2677-2016·2016-09-07

    Intuitive Surgical Recalls da Vinci EndoWrist Stapler 30 Instruments

    Intuitive Surgical is recalling 875 da Vinci EndoWrist Stapler 30 instruments due to reported shaft rotation interruptions and jaw opening failures.

    Product
    CURVED-TIP STAPLER 30,IS4000; Model number 470530; General and Plastic Surgery: The Intuitive Surgical da Vinci EndoWrist Stapler 30 Instrument and Stapler 30 Reloads are intended to be used with the da Vinci Xi Surgical System (Model IS4000) for resection, transection…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V647000·2016-09-07

    Volkswagen and Audi Recall 2015-2016 Models for Fuel Leak Fire Risk

    Volkswagen is recalling 2015-2016 Golf, GTI, and Audi A3 vehicles because a faulty fuel pump may cause leaks that increase fire risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN, AUDI GOLF, GTI, A3 CABRIOLET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2016-2016·2016-09-07

    Hampton Creek Muffin Mix Recalled for Salmonella in Coconut Milk Powder

    Hampton Creek Foods is recalling JUST Chocolate Chunk Muffin Mix because a positive test result for Salmonella was found in the coconut milk powder used in manufacturing.

    Product
    JUST Chocolate Chunk Muffin Mix; NET WT 20.8 oz. (1 lb 4.8 oz) 590 g); UPC 8 54829 00656 5. Ingredients: Muffin Mix: Enriched flours, {bleached (wheat flour, niacin, reduced Iron, thiamine mononitrate, riboflavin, folic acid), unbleached (Wheat flour, malted barley flour…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2012-2016·2016-09-07

    Pearson Foods Recalls Packaged Kale for Potential Salmonella Contamination

    Pearson Foods is voluntarily recalling specific lots of packaged kale due to potential Salmonella contamination. The product was distributed in Illinois, Michigan, and Wisconsin.

    Product
    Nappa Shredded 2/5 lb, packaged in plastic, keep refrigerated
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-2019-2016·2016-09-07

    Hampton Creek Devil's Food Cake Mix Recalled for Salmonella

    Hampton Creek Foods is recalling Devil's Food Cake Mix because a positive test found Salmonella in the coconut milk powder used in manufacturing.

    Product
    JUST Devil's Food Cake Mix; NET WT 20 oz. (1 lb 4 oz) 567 g); UPC 8 54829 00643 5. Ingredients: Muffin Mix: Enriched flours, {bleached (wheat flour, niacin, reduced Iron, thiamine mononitrate, riboflavin, folic acid), unbleached (Wheat flour, malted barley flour, niacin…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2681-2016·2016-09-07

    Philips PCR Compano Basic Reader Recalled for Power Supply Fire Hazard

    Philips is recalling 388 PCR Compano Basic Reader units because a defective power supply component can burn and release smoke.

    Product
    PCR Compano Basic Reader using 100-127V as mains voltage. Model numbers: 732027, 732028, and 732040. Radiological image processing system (Computed Radiography).
    Category
    Medical Device
    Distribution
    41 states
  • SevereFDA (Food)·F-2030-2016·2016-09-07

    Let's Do Lunch Recalls Chicken Patty Sandwiches for Listeria Risk

    Let's Do Lunch, Inc. is recalling Chicken Patty Sandwiches on a Whole Grain Bun due to potential Listeria monocytogenes contamination. The product was distributed in nine U.S. states.

    Product
    Chicken Patty Sandwich on a Whole Grain Bun Product ID 400003
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Devices)·Z-2692-2016·2016-09-07

    Beckman Coulter Recalls UniCel DxH Slidemaker Stainer Due to Fire Risk

    Beckman Coulter is recalling the UniCel DxH Slidemaker Stainer because flammable liquids may contact electrical components, posing a fire hazard.

    Product
    UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System, Catalog No. 775222 UniCel DxH Slidemaker Stainer (DxH SMS) Instructions for Use (IFU) Part Number B26647AC The DxH Slidemaker Stainer is a fully automated slide preparation and staining device that aspirates a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2008-2016·2016-09-07

    IFS Raw Shelled Pistachios Recalled for Potential Salmonella Contamination

    International Foodsource LLC is recalling raw shelled pistachios due to potential Salmonella contamination found in FDA testing.

    Product
    IFS Club Bag Pistachio Raw Shelled 80% Wholes Net Wt. 3 lb. (1 kg) International Foodsource LLC 52 Richboynton Rd. Dover NJ 07801 UPC 790429243026
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V640000·2016-09-06

    Acura Recalls 2015 TLX Vehicles for Transmission Wire Harness Defect

    Honda is recalling 2015 Acura TLX vehicles because transmission wire harness connections may have insufficient crimps, causing the vehicle to unexpectedly shift to neutral and increasing crash risk.

    Product
    ACURA — ACURA TLX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V641000·2016-09-06

    Audi Recalls 2017 Q7 Vehicles for Third-Row Seat Back Defect

    Volkswagen Group of America is recalling 2017 Audi Q7 vehicles because the third-row seat back may move forward in a crash, increasing injury risk.

    Product
    AUDI — AUDI Q7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V643000·2016-09-06

    Ford Recalls Multiple Models Due to Door Latch Defect

    Ford is recalling specific 2012-2016 vehicles because door latches may break, allowing doors to open while driving.

    Product
    FORD — FORD, LINCOLN MUSTANG, ESCAPE, TRANSIT CONNECT, MKC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V636000·2016-09-02

    Nissan Recalls Maxima and Murano Models Due to Brake Fluid Leak Fire Risk

    Nissan is recalling certain 2015-2017 Maxima and Murano vehicles because brake fluid may leak onto an electrical circuit board, increasing the risk of a fire.

    Product
    NISSAN — NISSAN MAXIMA, MURANO HYBRID, MURANO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V635000·2016-09-01

    Kaufman Recalls 2015-2016 Mini Car Haulers Due to Suspension Defect

    Kaufman Trailers is recalling 285 model year 2015-2016 Mini 5-Car Haulers because a suspension spring eye may break, allowing the axle to slide and increasing crash risk.

    Product
    KAUFMAN — KAUFMAN MINI CAR HAULER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16257·2016-09-01

    Polaris Recalls RZR XP Turbo Vehicles Due to Fire and Burn Hazards

    Polaris is recalling approximately 13,000 RZR XP Turbo recreational off-highway vehicles because engine overheating and loose drain tubes can cause fires and severe burn injuries.

    Product
    Recreational Off-Highway Vehicles (ROVs)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16T013000·2016-09-01

    Goodyear Recalls G399A LHS Tires Due to Tread Separation Risk

    Goodyear is recalling specific G399A LHS tires due to a manufacturing defect that may cause tread separation, increasing the risk of a crash.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1978-2016·2016-08-31

    SM Fish Corp. Recalls Herring Due to Listeria Contamination Risk

    SM Fish Corp. is recalling Ossie's Taam Shabbos Herring because the manufacturing plant tested positive for Listeria monocytogenes. The product was distributed in New York and New Jersey.

    Product
    OSSIE'S TAAM SHABBOS HERRING, NET WT. 7 OZ., UPC 739885109057; -- Far Rockaway, NY 11691 --- The product is packed in a plastic deli tub.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-1989-2016·2016-08-31

    SM Fish Corp. Recalls Ossie's Pickled Lox Due to Listeria Risk

    SM Fish Corp. is recalling Ossie's Pickled Lox because the manufacturing plant tested positive for Listeria monocytogenes. The product was distributed in New York and New Jersey.

    Product
    OSSIE'S PICKLED LOX, NET WT. 8 OZ., UPC 739885104137; -- Far Rockaway, NY 11691 --- The product is packed in a plastic deli tub.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-1980-2016·2016-08-31

    SM Fish Corp. Recalls Ossie's Wasabi Herring Due to Listeria Risk

    SM Fish Corp. is recalling Ossie's Wasabi Herring because the manufacturing plant tested positive for Listeria monocytogenes. The product was distributed in New York and New Jersey.

    Product
    OSSIE'S WASABI HERRING, NET WT. 7 OZ., UPC 739885109088; -- Far Rockaway, NY 11691 --- The product is packed in a plastic deli tub.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-2614-2016·2016-08-31

    Cook Inc. Recalls Slip-Cath Beacon Tip Catheters Due to Tip Fracture

    Cook Inc. is recalling Slip-Cath Beacon Tip Catheters because polymer degradation can cause the tip to fracture or separate, potentially leading to device fragments in the body.

    Product
    Slip-Cath Beacon Tip Catheter Catheter, Intravascular, Diagnostic The catheters are intended for use in angiographic procedures by physicians trained and experienced in angiographic techniques.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2597-2016·2016-08-31

    Conmed Pediatric ThermoGard Electrodes Recalled for Burn Risk

    Conmed is recalling Pediatric ThermoGard Dual Dispersive Electrodes because they may be incompatible with some electrosurgical generators, posing a risk of undetected pad lift and potential burns.

    Product
    Pediatric ThermoGard¿ Dual Dispersive Electrodes (for patients 5-15 kg.), 10' (3.05m) Cable, Catalog Number 51-7710. Intended to be used for the dispersion and return to the electrosurgical generator.
    Category
    Medical Device
    Distribution
    45 states