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.

Filters

Agency

Category

Minimum severity

Clear filters

17376–17400 of 39601

  • SevereFDA (Drugs)·D-1113-2018·2018-08-29

    Hetero Labs Recalls Valsartan Tablets Due to Carcinogen Impurity

    Hetero Labs Limited is recalling Valsartan tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.

    Product
    VALSARTAN — VALSARTAN (VALSARTAN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1114-2018·2018-08-29

    Hetero Labs Recalls Valsartan Tablets Due to Carcinogen Impurity

    Hetero Labs Limited is recalling Valsartan tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.

    Product
    VALSARTAN — VALSARTAN (VALSARTAN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2741-2018·2018-08-29

    Compass Health Brands Recalls CPAP Mask Cushions Due to Design Incompatibility

    Compass Health Brands is recalling CPAP mask cushions because a design change makes them incompatible with previous elbow parts, potentially causing unacceptable CO2 porting.

    Product
    CPAP Mask Cushion, Model Nos. PB781S, PB781M, PB781L, 781S, 781M and 781L Product Usage: A CPAP mask is attached to an end user s face and a CPAP machine, to treat end users with sleep apnea. The replacement cushion is a non-durable component that requires replacement every…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V567000·2018-08-28

    MAC Trailers Recalls 2019 Dump and Waste Trailers for Wheel Nut Defect

    MAC Trailer Mfg. is recalling 2019 Dump and Waste trailers because the wheel end nut locking device may not be properly installed, allowing the wheel end to separate from the axle.

    Product
    MAC TRAILERS — MAC TRAILERS WASTE TRAILER, DUMP TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E087000·2018-08-28

    Dexter D44 Trailer Axles Recalled for Potential Bearing Failure

    Dexter Axle is recalling D44 trailer axles with 4,400-pound capacity because missing inner bearing races can cause hub overheating or bearing failure.

    Product
    SUSPENSION:REAR:AXLE:NON-POWERED AXLE ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·18762·2018-08-27

    Polaris Recalls 2018 RZR XP Turbo S Vehicles Due to ROPS Fracture Hazard

    Polaris is recalling about 1,300 model year 2018 RZR XP Turbo S recreational off-highway vehicles because the rollover protection structure can fracture during high-speed rollovers.

    Product
    Model year 2018 RZR XP Turbo S recreational off-highway vehicles (ROVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V565000·2018-08-27

    Fabform Recalls 2018 EPT Dump Trailers Due to Hinge Fracture Risk

    Fabform is recalling 2018 EPT dump trailers because welded hinges may fracture, causing the dump box to fall unexpectedly and increasing the risk of injury or death.

    Product
    FABFORM — FABFORM DUMP TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V564000·2018-08-27

    Jayco Recalls 2015-2017 Redhawk Motorhomes Due to Fire Risk

    Jayco is recalling 2015-2017 Redhawk motorhomes because liquid leakage into the driver's power window switch can cause corrosion and increase the risk of a fire.

    Product
    JAYCO — JAYCO REDHAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·PHA-08242018-01·2018-08-24

    USDA Issues Public Health Alert for Empire Kosher Raw Chicken Due to Salmonella

    USDA FSIS issued a public health alert for Empire Kosher raw chicken products sold from September 2017 to June 2018 due to a link with a Salmonella outbreak.

    Product
    FSIS Issues Public Health Alert for Empire Kosher Poultry, Inc. Raw Chicken Products due to Possible Salmonella Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·069-2018·2018-08-23

    Cargill Recalls Ground Beef Due to Possible E. coli O157:H7 Contamination

    Cargill Meat Solutions is recalling approximately 25,288 pounds of ground beef products that may be contaminated with E. coli O157:H7. The products were shipped to warehouses in California and Colorado.

    Product
    Cargill Meat Solutions — Cargill Meat Solutions Recalls Ground Beef Products due to Possible E. coli O157:H7 Contamination
    Category
    Food
    Distribution
    2 states
  • SevereNHTSA·18V559000·2018-08-23

    REV Recalls 2018-2019 Motorhomes Due to Generator Exhaust Fire Risk

    REV Recreation Group is recalling 2018-2019 Fleetwood Pulse and Holiday Rambler Prodigy motorhomes because the generator exhaust pipe may contact the waste tank, increasing fire risk.

    Product
    HOLIDAY RAMBLER — HOLIDAY RAMBLER, FLEETWOOD PRODIGY, PULSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V556000·2018-08-23

    RAM 1500 Recall for Rear Differential Oil Level Defect

    Chrysler is recalling 2018-2019 RAM 1500 trucks because the rear differential may be underfilled, which could cause axle failure and increase crash risk.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V561000·2018-08-23

    Thomas Built Buses Saf-T-Liner C2 School Bus Seat Recall

    Daimler Trucks North America is recalling 2017-2019 Thomas Built Buses Saf-T-Liner C2 school buses because seat mounting feet may pull through the floor joint in a crash.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1828-2018·2018-08-22

    MBG Marketing Recalls Naturipe Blueberries Due to Salmonella Contamination

    MBG Marketing is recalling 1,320 boxes of Naturipe Blueberries because the product tested positive for Salmonella. The affected product was distributed to New York.

    Product
    naturipe Blueberries, INDIVIDUAL QUICK FROZEN, NET WT 30-LBS cardboard boxes, DISTRIBUTED BY NATURIPE 04726 COUNTY ROAD 215, GRAND JUNCTION, MN 43058
    Category
    Food
    Distribution
    1 state
  • CriticalCPSC·18199·2018-08-22

    Vornado VH101 Electric Space Heaters Recalled Due to Fire and Death

    Vornado Air is recalling VH101 Personal Vortex electric space heaters because they can overheat, posing fire and burn hazards. One death and 19 fire reports have been linked to the units.

    Product
    VH101 Personal Vortex electric space heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1085-2018·2018-08-22

    Ranier's Compounding Laboratory Recalls Morphine Sulf Inhalation Due to Sterility Concerns

    Ranier's Compounding Laboratory is recalling 60 vials of Morphine Sulf inhalation because practices at the firm may call into question the sterility of the product.

    Product
    Morphine Sulf inhalation, 5mg/3cc, 3cc per vial, Rx only, Ranier's Rx Laboratory, 1107 Lowry Avenue Suite A, Jeannette, PA 15644.
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1090-2018·2018-08-22

    Ranier's P/P/P Injection Recalled for Sterility Assurance Concerns

    Ranier's Compounding Laboratory is recalling P/P/P Injection vials because practices at the firm may call into question the sterility of the products.

    Product
    P/P/P (Prostaglandin/Papaverine/Phentolamine) Injection, 0.02/30/2 mg/mL, 5 mL vial, Rx only, Ranier's Rx Laboratory, 1107 Lowry Avenue Suite A, Jeannette, PA 15644.
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1077-2018·2018-08-22

    Lupin Recalls Lisinopril Tablets Due to Metal Contaminant

    Lupin Pharmaceuticals is recalling specific lots of Lisinopril tablets because a metal contaminant was found in one tablet.

    Product
    LISINOPRIL — LISINOPRIL (LISINOPRIL)
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-1096-2018·2018-08-22

    Northwind Recalls Valsartan HCTZ Tablets Due to Carcinogen Impurity

    Northwind Pharmaceuticals is recalling 43 bottles of Valsartan HCTZ 160/12.5mg tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.

    Product
    Valsartan HCTZ, 160/12.5mg, 30 tablets per bottle, Rx Only, Repackaged By: Northwind Pharmaceuticals, Indianapolis, IN 46256. NDC: 51655-950-52
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1092-2018·2018-08-22

    Ranier's Compounding Laboratory Recalls Prostaglandin Injection Due to Sterility Concerns

    Ranier's Compounding Laboratory is recalling Pro/PA/PH/AT Injection in Pennsylvania due to a lack of assurance of sterility.

    Product
    PRO/PA/PH/AT 18mcg/1.8mg/ (Prostaglandin//Papaverine/Phentolamine/Atropine) Injection, 18mcg/1.8 mg/0.2 mg/0.02 mg/mL, 10 mL vial, Rx only, Ranier's Rx Laboratory, 1107 Lowry Avenue Suite A, Jeannette, PA 15644.
    Category
    Drug
    Distribution
    1 state