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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15126–15150 of 36683

  • SevereFDA (Devices)·Z-0861-2019·2019-02-27

    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/o trolley Government Bundle, Product 860355, 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-1014-2019·2019-02-27

    Sysco Recalls Fresh Pomegranates Due to Temperature Control Failure

    Sysco Charlotte is recalling fresh pomegranates because a cooler malfunction meant the fruit was not held at appropriate temperatures, potentially making it unsafe.

    Product
    PACKER POMEGRANATE FRESH¿
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-0860-2019·2019-02-27

    Philips PageWriter TC50 Recall for Battery Overheating and Ignition Risk

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

    Product
    PageWriter TC50 Government Bundle, Product 860429, 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-0855-2019·2019-02-27

    Philips PageWriter TC30 ECG Devices Recalled for Overheating and Ignition Risk

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

    Product
    PageWriter TC30, Product 860306, 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 (Drugs)·D-0504-2019·2019-02-27

    Torrent Pharma Recalls Losartan Potassium and Hydrochlorothiazide Tablets Due to Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium and Hydrochlorothiazide tablets because FDA labs found the impurity N-nitrosodimethylamine (NDEA) above acceptable levels.

    Product
    LOSARTAN POTASSIUM and HYDROCHLOROTHIAZIDE TABLETS, USP, 100 mg/12.5 mg, a) 90-count bottle (NDC: 13668-117-90), b) 1000-count bottle (NDC: 13668-117-10), Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana Inda
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0505-2019·2019-02-27

    Torrent Pharma Recalls Losartan Potassium and Hydrochlorothiazide Tablets Due to Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium and Hydrochlorothiazide tablets because FDA testing found the impurity N-nitrosodimethylamine (NDEA) above acceptable levels.

    Product
    LOSARTAN POTASSIUM and HYDROCHLOROTHIAZIDE TABLETS, USP 50 mg/12.5 mg, a) 90-count bottle (NDC: 13668-116-90), b) 1000-count bottle (NDC: 13668-116-10), Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana Inda
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0858-2019·2019-02-27

    Philips PageWriter TC Cardiograph Recall for Battery Overheating and Fire Risk

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

    Product
    PageWriter TC70 w/o trolley Government Bundle, Product 860353, 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 (Drugs)·D-0502-2019·2019-02-27

    Torrent Pharma Recalls Losartan Potassium Tablets Due to NDEA Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium Tablets, 50 mg, because FDA testing found the impurity N-nitrosodimethylamine (NDEA) above acceptable levels.

    Product
    LOSARTAN POTASSIUM TABLETS, USP, 50 mg, a) 30-count bottle (NDC: 13668-409-30), b) 90-count bottle (NDC: 13668-409-90), c) 1000-count bottle (NDC: 13668-409-10), Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana Inda
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0509-2019·2019-02-27

    ICU Medical Recalls 0.9% Sodium Chloride Injection Due to CGMP Deviations

    ICU Medical Inc. is voluntarily recalling 475,320 bags of 0.9% Sodium Chloride Injection due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    0.9% Sodium Chloride Injection, USP 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-7983-09
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0853-2019·2019-02-27

    Philips PageWriter TC70 Cardiograph Recall for Battery Overheating Risk

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

    Product
    PageWriter TC70, Product 860315, 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
  • SevereUSDA FSIS·023-2019·2019-02-26

    McAllen Cold Storage Recalls Frozen Basa Fillets Lacking Inspection

    McAllen Cold Storage is recalling approximately 51,942 pounds of frozen Basa fillets imported from Vietnam that were not presented for import re-inspection.

    Product
    McAllen Cold Storage, Ltd. — McAllen Cold Storage, Ltd. Recalls Siluriformes Fish Products Produced Without Benefit Of Inspection
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·19V122000·2019-02-26

    International LT and Prostar Trucks Recalled for Exhaust Bracket Crack Risk

    Navistar is recalling 2016-2020 International LT and 2017-2018 Prostar trucks because a cracked exhaust bracket could cause the tailpipe to detach, creating a road hazard.

    Product
    INTERNATIONAL — INTERNATIONAL PROSTAR, LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·022-2019·2019-02-26

    Sahlen Recalls Deli Ham Due to Possible Plastic Contamination

    Sahlen Packing Company is recalling approximately 13,224 pounds of ready-to-eat deli ham products that may contain plastic. The products were distributed to retail locations in six northeastern states.

    Product
    Sahlen Packing Company, Inc. — Sahlen Packing Company, Inc. Recalls Ready-To-Eat Deli Meat Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    6 states
  • CriticalNHTSA·19E016000·2019-02-25

    Takata Driver Air Bag Inflator Recall for Rupture Risk

    Takata is recalling certain driver frontal air bag inflators that may rupture due to propellant degradation, posing a risk of serious injury or death.

    Product
    AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·021-2019·2019-02-25

    Crazy-Fresh Recalls Chicken Caesar Salad Due to Undeclared Allergens

    Russ Davis Wholesale is recalling chicken Caesar salad products because they contain undeclared milk and anchovies. No adverse reactions have been reported.

    Product
    Russ Davis Wholesale, Inc. — Russ Davis Wholesale - Crazy-Fresh Recalls Chicken Products due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·19V123000·2019-02-25

    Jayco Recalls 2019 Embark Motorhomes Due to Brake Component Defect

    Jayco is recalling 2019 Embark motorhomes because missing or improperly installed cotter pins may cause brake actuator rods to detach, increasing stopping distance and crash risk.

    Product
    JAYCO — JAYCO EMBARK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19E015000·2019-02-25

    Meritor Recalls EX225 Disc Brake Calipers Due to Cracked Drive Pins

    Meritor is recalling specific EX225 disc brake calipers because cracked drive pins may fracture, causing the vehicle to pull to one side while braking and increasing crash risk.

    Product
    SERVICE BRAKES, AIR:DISC:CALIPER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V124000·2019-02-25

    Entegra Reatta Motorhomes Recalled for Front Brake Defect

    Entegra is recalling 2019 Reatta motorhomes because missing or improper cotter pins on front brakes may reduce stopping power and increase crash risk.

    Product
    ENTEGRA — ENTEGRA REATTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·020-2019·2019-02-23

    Bellisio Foods Recalls Frozen Pork Rib Patties Due to Foreign Matter

    Bellisio Foods is recalling frozen boneless pork rib patties that may contain glass or hard plastic. No injuries have been reported.

    Product
    Bellisio Foods, Inc. — Bellisio Foods Recalls Boneless Pork Rib Frozen Entrée Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·19V120000·2019-02-22

    Kia Recalls 2012-2016 Soul Vehicles Due to Engine Fire Risk

    Kia is recalling 2012-2016 Soul vehicles with 1.6L GDI engines because high exhaust temperatures may damage the catalytic converter, potentially causing engine failure or fire.

    Product
    KIA — KIA SOUL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·019-2019·2019-02-22

    Fulton Seafood Recalls Wild Caught Catfish Lacking Federal Inspection

    Fulton Seafood Inc. is recalling approximately 100,924 pounds of wild caught catfish produced without federal inspection. The products were distributed to retail locations in Texas.

    Product
    Fulton Seafood Inc. Recalls Siluriformes Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • SevereUSDA FSIS·018-2019·2019-02-22

    TV Food LLC Recalls Uninspected Frozen Catfish Products Nationwide

    TV Food LLC is recalling approximately 27,956 pounds of frozen catfish products because they were produced without federal inspection. Consumers are urged to discard or return the items.

    Product
    TV Food LLC. Recalls Siluriformes Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    1 state