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

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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

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Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

14426–14450 of 114160

  • HighFDA (Devices)·Z-2568-2024·2024-08-21

    Merit Medical convenience kits recalled for syringe leaks and breakage risks

    Merit Medical is recalling convenience kits containing syringes with quality defects including leaks and breakage. The recalled kits may pose a risk to patients undergoing vascular and cardiac procedures.

    Product
    Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: K22C (Vein Tray Angiography kit), REF: K09T-11796F K12T-01558G K12T-01558H K12T-01822 K12T-01852L K12T-02006J K12T-02054 K12T-02091G K12T-02102B…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2585-2024·2024-08-21

    Medical Device Recall: BD Kiestra Urine Culture Software May Cause Inaccurate Results

    Becton Dickinson & Co. is recalling the BD Kiestra Urine Culture Application due to a software issue that may cause inaccurate bacterial colony counts. This could impact patient diagnosis and treatment decisions.

    Product
    BD Kiestra Urine Culture Application Powered by BD Synapsys Informatics Solution; Catalog (Ref): 444900;
    Category
    Medical Device
    Distribution
    17 states
  • HighFDA (Food)·F-1702-2024·2024-08-21

    Full Circle Frozen Dessert Recalled for Undeclared Cashew Allergen

    Full Circle Coconut Milk Chocolate Almond Crunch frozen dessert is recalled due to undeclared cashews. Product labels show mismatch: carton states 'coconut milk' but top states 'cashew milk,' and product contains cashew milk.

    Product
    FULL CIRCLE market COCONUTMILK CHOCOLATE ALMOND CRUNCH NON0DAIRY FROZEN DESSERT 16 FLOZ (1PT) 473 mL UPC 0 36800 46964 8 DISTRIBUTED BY TOPCO ASSOCIATES LLC ELK GROVE VILLAGE, IL 60007
    Category
    Food
    Distribution
    3 states
  • HighNHTSA·24V627000·2024-08-21

    Morbark Recalls 2018-2024 Trailers Due to Electrical Fire Risk

    Alamo Group is recalling specific Morbark trailers because loose wires in the power module may cause electrical arcing and fire.

    Product
    MORBARK — MORBARK M20, EEGER BEEVER 1821, EEGER BEEVER 2131, EEGER BEEVER 2230
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2584-2024·2024-08-21

    Cepheid Sample Collection Device May Leak Causing Cross-Contamination Risk

    Cepheid specimen collection devices may leak after patient samples are inserted, creating risk of biohazard exposure and false positive test results. Affected devices are distributed in medical testing facilities worldwide.

    Product
    Cepheid, Sample Collection Device, Part: 900-0370
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2578-2024·2024-08-21

    Merit Medical convenience kits with recalled plastic syringes may leak or break

    Convenience kits from Merit Medical Systems containing recalled plastic syringes have identified quality issues including leaks and breakage that may pose a risk to patient health.

    Product
    Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Customer Procedure Kit (Angiography/Angioplasty kit), REF: K09T-01138 K09T-04484A K09T-04757F K09T-04835H K09T-07256D K09T-07588B K09T-07611K K09T-07649K…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2580-2024·2024-08-21

    VITROS Folate Reagent Pack Recalled for Delayed Test Results

    Ortho-Clinical Diagnostics is recalling VITROS Folate Reagent Pack due to fibrinogen precipitation causing delayed test results. The recall affects 18,467 units distributed worldwide.

    Product
    VITROS Immunodiagnostic VITROS Folate Reagent Pack 1/2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2638-2024·2024-08-21

    PICC Catheter Package Contains Wrong Length, Causing Procedural Delay

    Argon Medical Devices recalls PICC catheters that are mislabeled. Packages marked 26G/1.9Fr x 30cm actually contain 26G/1.9Fr x 50cm catheters, which could delay procedures.

    Product
    L-CATH PICC S/L Peripherally Inserted Central Catheter, 26Ga (1.9F) 0.60mm x 30cm, REF: 384539
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Food)·F-1705-2024·2024-08-21

    Fox's u-bet Vanilla Syrup Recalled for Potential Microbiological Contamination

    SUBCO Foods is recalling Fox's u-bet Vanilla Flavored Syrup due to bloated bottles and elevated pH and water activity levels that indicate potential microbiological contamination and food-borne illness risk.

    Product
    Fox's u-bet Vanilla Flavored Syrup, 20oz, UPC 070216241016, 12 retail units per wholesale case
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-1731-2024·2024-08-21

    Pariva Marinated Labneh Bites Recalled for Potential Mold Contamination

    Pariva LLC recalls Marinated Labneh Bites due to potential mold contamination. Approximately 4,261 units were distributed across seven states.

    Product
    Pariva Marinated Labneh Bites Rosemary Garlic; NET WT 8 OZ (225g); INGREDIENTS: YOGURT (CULTURED PASTEURIZED GRADE A MILK & CREAM, SKIM MILK, WHEY PROTEIN CONCENTRATE, SALT AND PECTIN), *SUNFLOWER OIL, *EXTRA VIRGIN OLIVE OIL, ROSEMARY SPICES; CONTAINS: MILK, Distributed by…
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-2545-2024·2024-08-21

    Discrete Chemistry Analyzer Recalled Due to Carousel Malfunction

    Beckman Coulter is recalling 59 units of its Access 2 Immunoassay System Analyzer due to misaligned index wheels causing carousel motion errors that disable the analyzer and cancel patient tests.

    Product
    Discrete photometric chemistry analyzer for clinical use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2622-2024·2024-08-21

    Salivary Testosterone ELISA Quality Control Failure Invalidates Test Results

    DRG International is recalling Salivary Testosterone ELISA kits (Model SLV-3013) due to out-of-range quality controls that invalidate test runs and delay patient results. The recall affects 257 units distributed nationwide in six states.

    Product
    Product Name: Salivary Testosterone ELISA Model/Catalog Number: SLV-3013 Product Description: An enzyme immunoassay for the quantitative in vitro diagnostic measurement of free active testosterone in saliva.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0633-2024·2024-08-21

    Hydrocortisone & Acetic Acid Otic Solution Recalled for Potency and Impurity Failures

    Taro Pharmaceuticals recalled Hydrocortisone 1% & Acetic Acid 2% Otic Solution (lot AD12890) due to failed impurity specifications and lower-than-established active ingredient levels during stability testing.

    Product
    Hydrocortisone 1% & Acetic Acid 2% Otic Solution, 10 mL bottle, Rx only, Mfg by: Taro Pharmaceuticals, Inc., Brampton, Ontario, Canada L6T 1C1, Distributed by: Taro Pharmaceuticals U.S.A., Inc., Hawthorne, NY 10532, NDC 51672-3007-01
    Category
    Drug
    Distribution
    0 states
  • SevereNHTSA·24V625000·2024-08-20

    MCI Recalls 2021 D45CRTeLE Buses Due to Battery Fire Risk

    Motor Coach Industries is recalling 2021 D45CRTeLE vehicles because a software error may cause battery damage and increase the risk of fire.

    Product
    MCI — MCI D45CRTELE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24T008000·2024-08-20

    Continental Recalls HDL2 DL+ Tires Due to Belt Separation Risk

    Continental is recalling specific HDL2 DL+ tires because an incorrect rubber compound may cause the steel belt to separate, potentially leading to a loss of vehicle control.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V621000·2024-08-19

    Audi Recalls E-Tron Models Due to Brake Pedal Detachment Risk

    Audi is recalling 2019-2024 E-Tron and E-Tron Sportback vehicles because a faulty fastener may cause the brake pedal to detach, increasing crash risk.

    Product
    AUDI — AUDI E-TRON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V620000·2024-08-19

    Kalmar Recalls 2016-2017 Ottawa T2 Trucks Due to Brake Defect

    Kalmar is recalling 2016-2017 Ottawa T2 6X4 vehicles because insufficient air tank volume reduces braking performance and increases crash risk.

    Product
    KALMAR — KALMAR OTTAWA T2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V622000·2024-08-19

    Northern Lite Truck Camper Recall for Cooktop Overheating Risk

    Northern Lite is recalling 2022-2024 Truck Campers because a cooktop circuit board may overheat, increasing the risk of a fire.

    Product
    NORTHERN LITE — NORTHERN LITE TRUCK CAMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·024-2024·2024-08-16

    Perdue Recalls Frozen Chicken Nuggets and Tenders Due to Metal Contamination

    Perdue Foods is recalling approximately 167,171 pounds of frozen, ready-to-eat chicken breast nuggets and tenders due to possible metal wire contamination.

    Product
    Perdue Foods LLC — Perdue Foods LLC, Recalls Frozen, Ready-To-Eat Chicken Breast Nugget and Tender Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·24V616000·2024-08-16

    Forest River Recalls 2025 R-POD Travel Trailers Due to Fire Risk

    Forest River is recalling 2025 R-POD RPT203 travel trailers because the exterior griddle may be stowed while connected to the LP gas line, increasing fire risk.

    Product
    FOREST RIVER — FOREST RIVER R-POD
    Category
    Vehicle
    Distribution
    Distributed nationwide