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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37326–37350 of 39778

  • SevereFDA (Devices)·Z-1830-2012·2012-07-04

    Arrow Central Venous Catheter Recall for Labeling Inconsistency

    Arrow International is recalling 634,912 central venous catheter sets because the product label states 'contains no medication' while the insert indicates the product is medicated.

    Product
    Arrow Two-Lumen Central Venous Catheterization Set with Blue FlexTip(R) ARROWgard Blue(R) Catheter Product Usage: The multiple-lumen catheter permits venous access to central circulation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1679-2012·2012-07-04

    Crispy Almond Cake Rusk Recalled for Undeclared Milk Allergen

    Singh And Singh Distributors Inc. is recalling Crispy Almond Cake Rusk nationwide because the product may contain undeclared milk.

    Product
    Crispy by TWI Foods Almond Cake Rusk, Biscotte Croustillante Almande, Net Wt 750 g, Product of Canada Manufactured by TWI Foods Inc. 1869 Gage Court, Mississauga, Ont, Canada L5S 1S3.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1826-2012·2012-07-04

    Fresenius NaturaLyte Liquid Acid Concentrate Recalled for Alkalosis Risk

    Fresenius Medical Care is recalling NaturaLyte Liquid Acid Concentrate due to a risk of alkalosis. The product is used for hemodialysis.

    Product
    Fresenius NaturaLyte Liquid Acid Concentrate Product Codes: 08-0231-4, 08-1001-0, 08-1201-8, 08-1231-3, 08-1251-1, 08-1301-4, 08-2201-5, 08-2231-2, 08-2251-0, 08-2301-3,08-2351-8,08-3201-4,08-3231-1,08-3251-9,08-3301-2,08-4123-1, 08-4223-7, 08-4225-1' 08-4230-2, 08-4231-0…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1395-2012·2012-07-04

    Lloyd Inc Recalls Subpotent Thyro-Tab 0.75 mg Tablets

    Lloyd Inc is recalling 1,913,236 Thyro-Tab 0.75 mg tablets because they failed potency testing at the 6-month interval.

    Product
    Thyro-Tab.075 mg., packaged in bulk drums for repackaging. The firm name on the label is Lloyd Pharmaceutical, Shenandoah, Iowa 51601.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1883-2012·2012-07-04

    Terumo Recalls Sarns Antegrade Cardioplegia Cannula Due to Foreign Substance

    Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannulas because a foreign substance on the inner surface of some tips can be dislodged.

    Product
    X-COATED SMALL PATIENT PACK Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1893-2012·2012-07-04

    Terumo Recalls Sarns Antegrade Cardioplegia Cannula Kits Due to Foreign Substance

    Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannula kits because a foreign substance was found on the inner surface of some cannula tips that could dislodge.

    Product
    CPB CATHETER KIT-DR VANTRIGHT Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1673-2012·2012-07-04

    Grand Supercenter Recalls Frozen Oysters Due to Norovirus Contamination

    Grand Supercenter Inc. is recalling frozen oysters nationwide because inspectional evidence and illness reports indicate the products were prepared under insanitary conditions and may be contaminated with norovirus.

    Product
    Frozen Oysters: 1) I.Q.F. 2 LB/12 Frozen Oyster (Permit #NJ36RS) - Item #33200115.; I.Q.F. (T-Size) 8 oz/40 Frozen Oyster (Permit #NJ36RS) - Item #33200116; BLOCK 1 LB/30 Frozen Oyster (Permit #NJ36RS) - Item #33200117. I.Q.F. (S Size) 5 LB/6 Frozen Oyster (Permit #NJ36RS)…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·12215·2012-07-03

    Innovage Recalls Discovery Kids Lamps Due to Fire and Burn Hazards

    Innovage is recalling Discovery Kids Animated Marine and Safari Lamps because internal wires can cause short-circuiting, sparking, and fire.

    Product
    Discovery Kids™ Animated Marine and Safari Lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V310000·2012-07-02

    Zero Motorcycles Recalls 2012 Models Due to Battery Short Circuit Risk

    Zero Motorcycles is recalling 254 model year 2012 motorcycles because insufficient weatherproofing may cause a battery short circuit in wet conditions, leading to sudden power loss.

    Product
    ZERO — ZERO XU-LSM, ZERO S, X, ZERO DS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V309000·2012-07-02

    Prevost Recalls 98 Buses Due to Fire Suppression System Defect

    Prevost is recalling 98 model year 2008-2010 buses because the fire suppression system may activate without a fire, causing an unplanned stop and increasing crash risk.

    Product
    PREVOST — PREVOST H3-45, XLII-45E, X3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V306000·2012-06-29

    Isuzu Recalls Amigo and Rodeo Sport for Rear Suspension Corrosion

    Isuzu is recalling 1998-2002 Amigo and Rodeo Sport vehicles in 21 states and D.C. due to rear suspension corrosion that may increase crash risk.

    Product
    ISUZU — ISUZU RODEO SPORT, AMIGO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12E025000·2012-06-29

    Thunderbird Brake Hose Recall for Non-Compliant Federal Safety Standards

    Thunderbird Headquarters is recalling specific brake hoses for 1955-1966 Ford Thunderbirds that fail to meet federal safety standards, posing a risk of brake fluid leaks.

    Product
    SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:HOSES, LINES/PIPING, AND FITTINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V305000·2012-06-29

    Toyota Recalls 164,601 Vehicles for Accelerator Pedal Sticking Hazard

    Toyota is recalling 164,601 Lexus and Land Cruiser vehicles because the accelerator pedal can get stuck open by floor mats, posing a crash risk.

    Product
    LEXUS — LEXUS, TOYOTA RX350, RX HYBRID, LAND CRUISER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12T014000·2012-06-29

    TBC Recalls Mirada and Big Foot Tires Due to Sidewall Separation Risk

    TBC Corporation is recalling specific Mirada and Big Foot tires due to a manufacturing anomaly that may cause sidewall cracks or separation, potentially leading to rapid air loss and vehicle crashes.

    Product
    TIRES:SIDEWALL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V307000·2012-06-29

    Zero Motorcycles Recalls 2011-2012 Models Due to Brake Light Switch Defect

    Zero Motorcycles is recalling certain 2011 and 2012 models because the front brake light switch may not activate until significant lever travel occurs, potentially failing to alert following drivers.

    Product
    ZERO — ZERO XD, XU, ZERO DS, ZERO XU
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V300000·2012-06-28

    Prevost Recalls 2012 Buses Due to Steering Gearbox Bolt Issue

    Prevost is recalling certain 2012 VIP 45, XLII, and X3-45 vehicles because steering gearbox bolts may be too long to be sufficiently torqued, potentially leading to reduced steering function.

    Product
    PREVOST — PREVOST VIP 45, XLII, X3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·12211·2012-06-28

    Hot Spring Spas and Limelight Hot Tubs Recalled Due to Fire Hazard

    Watkins Manufacturing is recalling about 5,600 Hot Spring Spas and Limelight Hot Tubs because loose electrical connections can cause overheating and fire.

    Product
    Hot Spring Spas and Limelight Hot Tubs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·12206·2012-06-28

    Rigo Recalls Children's Lounge Pants and Boxers for Flammability Violation

    Rigo International is recalling about 210,000 children's lounge pants and boxers sold at Academy because they fail federal flammability standards, posing a burn risk.

    Product
    Boys and Girls Pull-On Lounge Pants and Girls Boxers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·12212·2012-06-28

    Harbor Breeze Bath Fans Recalled for Fire Hazard

    Delta Electronics is recalling Harbor Breeze bath fans sold at Lowe's because the heater blades can fail, causing overheating and fire.

    Product
    Harbor Breeze Bath Fans with Heater and Light
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1476-2012·2012-06-27

    Indonesian Food Mart Recalls Tempeh Super Starter Yeast Due to Salmonella

    Indonesian Food Mart is recalling Tempeh Super Starter Yeast because the imported product tested positive for Salmonella. The product was distributed nationwide and internationally.

    Product
    Tempeh Super Starter Yeast, Rhizopus Oligosporus cultures, soybean rice flour, packaged in clear plastic packages in 30 gm, 50 gm, 250 gm, and 1000 gm sizes and labeled in part ***Indonesianfoodmart.com***
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1463-2012·2012-06-27

    Santos Cinnamon Sticks Recalled for Undeclared Peanut and Wheat Traces

    Santos Inc. is recalling cinnamon sticks because they were packaged on equipment shared with peanuts and wheat, posing an allergen risk.

    Product
    Santos Brand, Cinnamon Sticks packed in clear plastic bags, 7oz, 14oz
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-1475-2012·2012-06-27

    Indonesian Food Mart Recalls Tempeh Starter Yeast for Salmonella

    Indonesian Food Mart is recalling Tempeh Starter Yeast because it tested positive for Salmonella. The product was distributed nationwide and internationally.

    Product
    Tempeh Starter Yeast, Rhizopus Oligosporus cultures, soybean rice flour, Original, packaged in clear plastic packages in 30gm, 50gm, 250 gm, and 1000 gm sizes and labeled in part ***Indonesianfoodmart.com***
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1386-2012·2012-06-27

    Physicians Total Care Recalls Morphine Sulfate Tablets Due to Labeling Error

    Physicians Total Care is recalling Morphine Sulfate tablets because bottles may be mislabeled, potentially containing the wrong formulation.

    Product
    Morphine Sulfate Immediate Release tablet, 30 mg/120 tablet bottles, Rx only, Physician Total Care, Inc, Tulsa, OK 74146-6234, NDC 54868-4973-00
    Category
    Drug
    Distribution
    1 state