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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15101–15125 of 36683

  • SevereNHTSA·19V332000·2019-03-01

    Prime-Time Recalls 2016-2018 Ram ProMaster and Ford Transit Vehicles

    Prime-Time Specialty Vehicles is recalling 2016-2018 Ram ProMaster and Ford Transit vans with Freedman GO-ES Foldaway Seats because the seat cushions may not stay locked during a crash.

    Product
    RAM — RAM, FORD PROMASTER, TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V152000·2019-03-01

    Terex Advance Recalls 2018-2019 Concrete Mixer Trucks for Brake Defect

    Terex Advance is recalling 2018-2019 Front Discharge Concrete Mixer Trucks because cracked drive pins in the brake calipers may fracture, causing loss of vehicle control.

    Product
    TEREX ADVANCE — TEREX ADVANCE FRONT DISCHARGE CONCRETE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V146000·2019-02-28

    A-1 Auto Electric Recalls 2015 Freightliner CNG Vehicles for Valve Defect

    A-1 Auto Electric is recalling 2015 Freightliner 1085D and M2 refuse vehicles modified for CNG. A valve snap ring may fail if overtightened, risking injury or fire.

    Product
    FREIGHTLINER — FREIGHTLINER 1085D, M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V143000·2019-02-28

    Chrysler Recalls 2018 Pacifica Models Due to Control Arm Separation Risk

    Chrysler is recalling 47,771 2018 Pacifica and Pacifica Plug-In Hybrid vehicles because the right front lower control arm may separate, increasing crash risk.

    Product
    CHRYSLER — CHRYSLER PACIFICA PLUG-IN HYBRID, PACIFICA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V141000·2019-02-28

    McLaren Recalls Vehicles Due to Passenger Air Bag Inflator Explosion Risk

    McLaren is recalling specific 2012-2017 models because passenger air bag inflators may explode due to propellant degradation, posing a risk of serious injury or death.

    Product
    MCLAREN — MCLAREN MP4-12C SPIDER, 675 LONGTAIL, P1, 570
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0943-2019·2019-02-27

    Satur Farms Baby Spinach Recalled for Potential Salmonella Contamination

    Satur Farms LLC is recalling baby spinach due to potential Salmonella contamination. The product was distributed to New York, Florida, Connecticut, and New Jersey.

    Product
    SATUR FARMS BABY SPINACH Retail product is packed in plastic clamshell containers with Satur Farms brand name: 5 oz, 10 oz, 16 oz Food service product is packed in sealed poly bags: 2-1/2 lbs, 3#, 4#, 4 x 2.5#, 4 x 3#
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-0944-2019·2019-02-27

    Satur Farms Mesclun Salad Recalled Due to Salmonella Contamination Risk

    Satur Farms LLC is recalling Mesclun Salad products due to potential Salmonella contamination. The recall affects retail and food service products distributed to New York, Florida, Connecticut, and New Jersey.

    Product
    SATUR FARMS MESCLUN SALAD Retail product is packaged in clamshell containers with Satur Farms Brand Name: 5 oz, 10 oz, 16 oz Food service product is packed in sealed poly bags: 2-1/2 lbs, 3#, 4#, 4 x 2.5#, 4 x 3#
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-0857-2019·2019-02-27

    Philips PageWriter TC70 Cardiograph Recall for Battery Overheating Risk

    Philips is recalling 57 PageWriter TC70 cardiographs because end-of-life batteries may overheat, melt, or ignite, posing a risk of injury to patients and users.

    Product
    PageWriter TC70 w/trolley Government Bundle, Product 860352, Software revisions up to and including A.07.05. 22 to evaluate the electrocardiogram of adult and pediatric patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0960-2019·2019-02-27

    Sysco Recalls Block and Barrel Cheddar Cheese Due to Temperature Issues

    Sysco Charlotte is recalling Block and Barrel Imperial Cheddar cheese because a cooler malfunction may have compromised food safety.

    Product
    Block and Barrel Imperial CHEESE CHEDDAR X SHARP LOAF YW 2/5 LB cases
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0508-2019·2019-02-27

    US Compounding Recalls Ephedrine Sulfate Syringes Due to Sterility Concerns

    US Compounding Inc is recalling 1,686 syringes of Ephedrine Sulfate 50 mg/10 mL because the company cannot ensure the product is sterile.

    Product
    Ephedrine Sulfate, 50 mg/10 mL, 10 mL Single Use Syringe, Rx only, US Compounding Pharmacy 1270 Don's Lane Conway, AR 800-718-3588, Barcode: 62295308407
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0850-2019·2019-02-27

    Baxter Recalls Kaguya Automated Peritoneal Dialysis Systems Due to Software Defect

    Baxter Healthcare is recalling 1,085 Kaguya Automated Peritoneal Dialysis Systems because a software defect may cause shortened dwell times during therapy.

    Product
    Kaguya Automated Peritoneal Dialysis System Product Usage: It is intended for automatic control of dialysate solution exchanges in the treatment of adult renal failure patients undergoing Peritoneal dialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1001-2019·2019-02-27

    Sysco Recalls Majestic Blue Crab Meat Due to Temperature Control Failure

    Sysco Charlotte is recalling Majestic Blue Crab Meat Super Lump because a cooler malfunction meant the product was not held at appropriate temperatures, potentially making it unsafe.

    Product
    Majestic Blue CRAB MEAT SUPER LUMP PAST MEX
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-0854-2019·2019-02-27

    Philips PageWriter TC50 ECG Devices Recalled for Overheating and Fire Risk

    Philips is recalling PageWriter TC50 electrocardiogram devices because end-of-life batteries may overheat, melt the case, or ignite, posing a risk of injury to patients and users.

    Product
    PageWriter TC50, Product 860310, Software revisions up to and including A.07.05.22 used to evaluate the electrocardiogram of adult and pediatric patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V135000·2019-02-27

    BMW Recalls 2019 X7 Models Due to Loose Seat Adapter Bolts

    BMW is recalling 2019 X7 vehicles with the business lounge seat option because seat adapter bolts may not be properly tightened, increasing injury risk in a crash.

    Product
    BMW — BMW X7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1050-2019·2019-02-27

    Boston Smoked Fish Company Recalls Nova Lox Sides Due to Low Salt Levels

    The Boston Smoked Fish Company is recalling Nova Lox Sides because the product had low water phase salt levels. The recall affects 29.45 lbs distributed in Massachusetts.

    Product
    BOSTON SMOKED FISH CO. Nova Lox Sides, 5 packages of 2 pound units in corrugated box, Store at or below 38 deg, UPC: (01)90857016007065(3202)100000
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0501-2019·2019-02-27

    Torrent Pharma Recalls Losartan Potassium Tablets Due to NDEA Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium Tablets, USP, 100 mg, because FDA testing found the impurity N-nitrosodimethylamine (NDEA) above the interim acceptable daily intake level.

    Product
    LOSARTAN POTASSIUM TABLETS, USP, 100 mg, a) 30-count (NDC: 13668-115-30), b) 90-count (NDC: 13668-115-90), c) 1000-count (NDC: 13668-115-10) per bottle, Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana Inda
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0503-2019·2019-02-27

    Torrent Pharma Recalls Losartan Potassium Tablets Due to NDEA Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium Tablets because FDA testing found the impurity NDEA above acceptable levels.

    Product
    LOSARTAN POTASSIUM TABLETS, USP, 25 mg, 90-count bottle (NDC: 13668-113-90), Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana Inda
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0859-2019·2019-02-27

    Philips PageWriter TC30 Cardiograph Recall for Battery Overheating Risk

    Philips is recalling PageWriter TC30 cardiographs because end-of-life batteries may overheat, melt, or ignite, posing injury risks to patients and users.

    Product
    PageWriter TC30 w/ trolley Government Bundle, Product 860354, Software revisions up to and including A.07.05.22 to evaluate the electrocardiogram of adult and pediatric patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0856-2019·2019-02-27

    Philips PageWriter TC20 Recall for Battery Overheating and Fire Risk

    Philips is recalling PageWriter TC20 devices because end-of-life batteries may overheat, melt the case, or ignite, posing a risk of injury.

    Product
    PageWriter TC20, Product 860332, Software revisions up to and including A.07.05.22 to evaluate the electrocardiogram of adult and pediatric patients
    Category
    Medical Device
    Distribution
    Distributed nationwide