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 deaths or serious injuries are reported, 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

10026–10050 of 36631

  • SevereUSDA FSIS·005-2021·2021-02-19

    USDA Recalls Pork Pâté Imported Without Inspection

    AH Company International Distribution is recalling approximately 30,081 pounds of Monique Ranou pork pâté products imported without FSIS re-inspection.

    Product
    AH Company International Distribution, Inc., Recalls Pork Products Imported Without the Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V097000·2021-02-19

    KME Predator Fire Trucks Recalled for Insufficient Rear Axle Welds

    KME is recalling certain Predator fire trucks because rear axle welds may be insufficient, potentially causing loss of vehicle control and increasing crash risk.

    Product
    KME — KME PREDATOR PUMPER, PREDATOR RESCUE, PREDATOR PANTHER PUMPER, PREDATOR SS PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V100000·2021-02-19

    KME Recalls TDA Firetrucks Due to Trailer Brake Wiring Defect

    KME is recalling 2001-2020 TDA tractor-drawn aerial firetrucks because incorrect wiring in the trailer's ABS control module may cause brake failure, increasing crash risk.

    Product
    KME — KME TDA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21T002000·2021-02-19

    Cooper Tire Recalls Multiple Tires Due to Sidewall Separation Risk

    Cooper Tire is recalling specific Discoverer, Evolution, and other brand tires because the sidewall may bulge or separate, potentially causing a rapid deflation and crash.

    Product
    TIRES:SIDEWALL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V092000·2021-02-18

    Trail King Recalls 2021 TKSA Trailers Due to Frame Crack Risk

    Trail King is recalling 2021 TKSA trailers because a cross member in the slide pan frame may crack and detach, increasing crash risk.

    Product
    TRAIL KING — TRAIL KING TKSA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V090000·2021-02-18

    Ford F-Series Trucks Recalled for Potential Windshield Detachment in Crashes

    Ford is recalling certain 2020-2021 F-150 and Super Duty trucks because the windshield may not be properly bonded, risking detachment in a crash. Dealers will remove and reinstall the windshield at no cost.

    Product
    FORD — FORD F-450 SD, F-350 SD, F-250 SD, F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0262-2021·2021-02-17

    Apotex Recalls Enoxaparin Syringes Due to Labeling Mixup

    Apotex Corp. is recalling Enoxaparin Sodium Injection syringes because some barrels may display incorrect concentration markings, posing a risk of dosing errors.

    Product
    Enoxaparin Sodium Injection, USP 120 mg/ 0.8 mL Single Dose Syringes with Automatic Safety Device For Subcutaneous Injection 10 x 0.8 mL Single Dose Syringes Rx Only,Manufactured by: Gland Pharma Ltd. Hyderabad, India Manufactured for: Apotex Corp. Weston, FL 33326 NDC 60505-079
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0275-2021·2021-02-17

    Maine Grains Organic Yellow Peas Recalled for Undeclared Soy

    Maine Grains Inc. is recalling Organic Yellow Peas due to undeclared soy. The product was sold in various packaging formats across multiple states.

    Product
    Maine Grains Inc. brand Organic Yellow Peas sold between 10/17/2019 and 11/1/2020; product was packaged in 25lb bulk bags, 12 x 1lb cases; and clear cellophane 1lb bags sold online and labelled as "Crop Rotation Organic Yellow Peas"
    Category
    Food
    Distribution
    17 states
  • CriticalFDA (Food)·F-0279-2021·2021-02-17

    Sprout's Yogurt Covered Cranberries Recalled for Undeclared Almonds

    Ohio Hickory Harvest is recalling Sprout's Vanilla Flavored Yogurt Covered Cranberries due to undeclared almonds, a tree nut allergen.

    Product
    Sprout's Vanilla Flavored Yogurt Covered Cranberries UPC 646670463778 12 Ounce Stand-Up Pouch Bag Ambient Storage
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1084-2021·2021-02-17

    Wahl Heated Massager Recalled Due to Fire Hazard

    Wahl Clipper Corp is recalling 161 units of the WAHL 4212 Heated Massager because the connection between the massager and heat element can overheat, posing a fire hazard.

    Product
    WAHL 4212 HEATED MASSAGER, SKU F800000004212 - Product Usage: intended to relieve minor muscle aches and pains.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1073-2021·2021-02-17

    Argon Medical Devices Recalls Transjugular Liver Biopsy Systems

    Argon Medical Devices is recalling 863 TLAB Transjugular Liver Biopsy Systems due to a manufacturing error that may cause the sheath to separate during use.

    Product
    Argon Medical Devices TLAB, Transjugular Liver Biopsy System, REF: TL - 19, 1/19 GA Flexcore Biopsy Needle, 7F Introducer Sheath W/Curved Metal Stiffener, Tissue Removal Swabs, 5F Straight Catheter, 5F Curved Catheter, Sterile EO,
    Category
    Medical Device
    Distribution
    46 states
  • SevereFDA (Devices)·Z-1077-2021·2021-02-17

    Argon Medical Devices Recalls Transjugular Liver Biopsy Systems

    Argon Medical Devices is recalling 583 Transjugular Liver Biopsy Systems due to a manufacturing error that may cause the sheath to separate during use.

    Product
    Argon Medical Devices TLAB, Transjugular Liver Biopsy System, REF: TL - 18N, 1/18 GA Flexcore Biopsy Needle, 1/7F Introducer Sheath W/Curved Metal Stiffener, 4/Tissue Removal Swabs, Sterile EO,
    Category
    Medical Device
    Distribution
    46 states
  • SevereNHTSA·21V082000·2021-02-17

    Newmar motorhome brake light switches may fail to illuminate

    Newmar is recalling 2017–2021 Dutch Star and 2021 Kountry Star motorhomes because the brake light switch may chafe against the windshield wiper mechanism, preventing brake lights from illuminating. This increases crash risk.

    Product
    NEWMAR — NEWMAR DUTCH STAR, KOUNTRY STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0960-2021·2021-02-17

    Cook Medical Kwart Retro-Inject Ureteral Stent Set Recalled for Material Defect

    Cook Inc. is recalling 42 units of Kwart Retro-Inject Ureteral Stent Sets because they were manufactured with incorrect material, which may cause the stent to be stiffer and susceptible to degradation, breakage, or fragmentation.

    Product
    Cook Medical Kwart Retro-Inject Ureteral Stent Set 7.0Fr. 22-32cm -Used for retrograde injection during Extracorporeal Shock Wave Lithotripsy (E.S.W.L.) and leaving an indwelling ureteral stent Reference Part Number (RPN): 003700 GPN: G14837
    Category
    Medical Device
    Distribution
    6 states
  • SevereFDA (Devices)·Z-1074-2021·2021-02-17

    Argon Medical Devices Recalls Transjugular Liver Biopsy System Due to Sheath Separation

    Argon Medical Devices is recalling the TLAB Transjugular Liver Biopsy System because a manufacturing error may cause the sheath to separate during use, potentially requiring surgical intervention.

    Product
    Argon Medical Devices TLAB, Transjugular Liver Biopsy System, REF: TL - 19N, 1/19 GA Flexcore Biopsy Needle, 1.7F Introducer Sheath W/Curved Metal Stiffener, 4/Tissue Removal Swabs, Sterile EO,
    Category
    Medical Device
    Distribution
    46 states
  • SevereFDA (Drugs)·D-0252-2021·2021-02-17

    Lidocaine/Tetracaine Ointment Recalled for Higher Concentration Than Listed

    Stanley Specialty Pharmacy is recalling Lidocaine/Tetracaine ointment because the lidocaine concentration is higher than listed on the label.

    Product
    Lidocaine/Tetracaine (LIPO110)* 23%/7% Ointment 100 GMS per 4 ounce plastic ointment jar, Rx Only, Stanley Specialty Pharmacy 3120 Latrobe Dr. Suite 200 Charlotte, NC 28211
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V076000·2021-02-17

    Ford Recalls 2004-2006 Rangers for Air Bag Inflator Defect

    Ford is recalling 2004-2006 Ranger vehicles because certain replacement air bag inflators may explode during deployment, potentially causing serious injury or death.

    Product
    FORD — FORD RANGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0287-2021·2021-02-17

    EVR Foods Recalls LAVVA Blueberry Pili Nut Yogurt for Potential Mold

    EVR Foods Inc. is recalling LAVVA Blueberry Dairy Free Pili Nut Yogurt because the product may contain mold. The recall covers 806 cases distributed across 14 states.

    Product
    "LAVVA Blueberry Dairy Free Pili Nut Yogurt. NO SUGAR ADDED. NET WT 5.3OZ (150g) ***KEEP REFRIGERATED***DISTRIBUTED BY EVR FOODS INC. NEW YORK, NY 10010"
    Category
    Food
    Distribution
    14 states
  • SevereFDA (Devices)·Z-0990-2021·2021-02-17

    Aomori Olympus Electrosurgical Snare Recalled for Inadequate Package Seals

    Aomori Olympus is recalling SD-240U-25 electrosurgical snares because inspection found some sterile packages have inadequate seals, posing an infection risk.

    Product
    SD-240U-25 ELECTROSURGICAL SNARE, model no. SD-240U-25 - Product Usage: Used with endoscopes to electrosurgically resect tissue within the digestive tract.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1075-2021·2021-02-17

    Argon Medical Devices Recalls Transjugular Liver Biopsy Systems

    Argon Medical Devices is recalling 247 Transjugular Liver Biopsy Systems because a manufacturing error may cause the sheath to separate during use, potentially requiring surgical intervention.

    Product
    Argon Medical Devices TLAB, Transjugular Liver Biopsy System, REF: TL - 19S, 1/19 GA Flexcore Biopsy Needle, 1/7F Introducer Sheath W/Curved Metal Stiffener, 4/Tissue Removal Swabs, 1/5f straight catheter, Sterile EO,
    Category
    Medical Device
    Distribution
    46 states
  • SevereFDA (Food)·F-0278-2021·2021-02-17

    Reese Hollandaise Sauce Recalled Due to Compromised Vacuum Seals

    World Finer Foods is recalling Reese Hollandaise Sauce in 7.5 oz glass jars due to compromised vacuum seals and product expansion that may allow microorganism growth.

    Product
    Reese Hollandaise Sauce packaged in glass jars 7.5 oz UPC: 7067060108
    Category
    Food
    Distribution
    12 states
  • SevereFDA (Devices)·Z-1010-2021·2021-02-17

    Aomori Olympus ForceMax Injector Recalled for Inadequate Package Seal

    Aomori Olympus is recalling ForceMax Up injectors because some sterile packages have inadequate seals, posing a risk of infection if non-sterile equipment is used.

    Product
    INJECTOR FORCEMAX UP 2.8MMCH 21G 6MM, model no. NM-400L-0621 - Product Usage: Used with endoscopes to perform endoscopic injection for the treatment of esophageal and gastric varices and for submucosal injection in the digestive tract.
    Category
    Medical Device
    Distribution
    Distributed nationwide