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

22426–22450 of 26076

  • HighFDA (Food)·F-0845-2022·2022-03-16

    Chicago Sweet Connections Coffee Cake Recall Due to Undeclared Allergens

    Chicago Sweet Connections is recalling Coffee Cake - Cherry Flavor due to undeclared allergens (egg, milk, and wheat). Affected products were distributed to retail locations in Illinois and Wisconsin.

    Product
    Chicago Sweet Connections: Coffee Cake - Cherry Flavor packaged in an aluminum rectangular tray with plastic dome lid Single pack - 6 servings
    Category
    Food
    Distribution
    2 states
  • HighCPSC·22103·2022-03-16

    B. toys Wooden Activity Walker recalled for choking hazard

    B. toys Walk 'n' Learn wooden toddler walkers are being recalled because wheels and attachment hardware can detach in small pieces, creating a choking hazard for young children. Battat has received six reports of detachment, including one incident where a child placed a detached metal nut in her mouth.

    Product
    B. toys Wooden Activity Walker - Walk 'n' Learn
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0729-2022·2022-03-16

    Vascular Graft Mislabeled; Packaging Labels Do Not Match Product Specifications

    A vascular graft has been recalled due to labeling mismatch: the outer package label differs from the inner sterile packaging in graft type and dimensions. Implanting the wrong size could disrupt blood vessel connections and create a pseudo-aneurysm.

    Product
    HEMASHIELD GOLD KNITTED MICROVEL DOUBLE VELOUR VASCULAR GRAFT- D: 7 mm; L: 60 cm Indicated for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease. Product Code/REF Number: M002020952070
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0838-2022·2022-03-16

    Chicago Sweet Connections Paczkis Recall: Undeclared Egg, Milk, Wheat Allergens

    Chicago Sweet Connections is recalling Prune Flavor Paczkis (4-pack, UPC 841049024035) due to undeclared allergens: egg, milk, and wheat. Affected products were distributed to retail locations in Illinois and Wisconsin.

    Product
    Chicago Sweet Connections: Paczkis - Prune Flavor packaged in a clear plastic clamshell 4 pack
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0732-2022·2022-03-16

    Radiation therapy planning software displays wrong images during animation playback

    RayStation/RayPlan versions 6.0.0.24 through 9.2.0.483 incorrectly display selected images as both primary and secondary when animation playback is running, affecting treatment planning visualization.

    Product
    RayStation/RayPlan- designed for treatment planning and analysis of radiation therapy. Software Version: 6.0.0.24 , 6.1.0.26 , 6.1.1.2 , 6.2.0.7 , 6.3.0.6 , 7.0.0.19 , 8.0.0.61 , 8.0.1.10 , 8.1.0.47 , 8.1.1.8 , 8.1.2.5 , 9.0.0.113 , 9.1.0.933 , 9.2.0.483 . Includi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0735-2022·2022-03-16

    Laboratory diagnostic tips recalled for potential dispensing errors

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry VersaTips due to shape deformity that may reduce sample volume by 16%. Undetected errors could result in inaccurate test results for bloodborne infectious disease assays.

    Product
    VITROS Chemistry Products VersaTips, Catalog No. 6801715 A VersaTip sales unit is composed of 1000 tips per box.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0746-2022·2022-03-16

    PCA 4000 Dental Curing Units May Not Fully Cure Resins

    Envisiontec is recalling 172 PCA 4000 curing units that may not properly cure dental resins to specification (SKU ACC-06-1000).

    Product
    PCA 4000 Curing Units, SKU number ACC-06-1000 The PCA 4000 is used for curing industrial resins as well and this recall will not impact units sold to industrial customers.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·22102·2022-03-16

    RH Illuminated Mirrors Recalled Due to Fire and Shock Hazards

    RH is recalling about 3,300 illuminated mirrors sold from September 2015 through February 2022 due to loose components in bulb sockets that can cause overcurrent, overheating, fire, and electrical shock. Consumers should stop using them immediately and contact RH for a refund or replacement.

    Product
    Illuminated Mirrors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0816-2022·2022-03-16

    Banana Coconut Rum Cake Recalled for Undeclared Allergens

    Edible Spirits, Inc is recalling Banana Coconut Rum Cake because the product was not labeled with required allergen information including eggs, wheat, milk, and tree nuts.

    Product
    Banana Coconut Rum Cake
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0817-2022·2022-03-16

    Key Lime Rum Cakes Recalled for Undeclared Allergens

    Edible Spirits, Inc is recalling Key Lime Rum cakes due to failure to declare allergens (eggs, wheat, milk, tree nuts) on the label. Consumers with these allergies risk allergic reaction.

    Product
    Key Lime Rum
    Category
    Food
    Distribution
    0 states
  • SevereNHTSA·22V157000·2022-03-15

    2022 Winnebago travel trailers recalled for improperly welded couplers

    Winnebago is recalling certain 2022 Micro Minnie, Minnie, and Voyage travel trailers because the coupler was improperly welded, which may cause the trailer to separate from the tow vehicle and increase crash risk.

    Product
    WINNEBAGO — 2022 WINNEBAGO MICRO MINNIE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V154000·2022-03-14

    2021–2022 Dodge Durango and Jeep Grand Cherokee Steering Recall

    Chrysler is recalling 2021–2022 Dodge Durango and 2022 Jeep Grand Cherokee vehicles due to steering gear defect. The rack bar may have been insufficiently hardened, potentially causing loss of steering control.

    Product
    DODGE — 2021 DODGE DURANGO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V155000·2022-03-14

    2020 Audi S7 and Related Models: Fuel Gauge Malfunction Recall

    Volkswagen Group (Audi) is recalling certain 2019-2022 A6, A7, S6, S7, RS6 Avant, and RS7 vehicles because the fuel level sender may stick, causing inaccurate fuel gauge readings that could lead to engine stalls and crash risk.

    Product
    AUDI — 2020 AUDI S7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V143000·2022-03-11

    Forest River 2022 Travel Trailers Recalled for Coupler Weld Defect

    Forest River is recalling certain 2022 travel trailers due to improperly welded couplers that may cause trailer separation from the tow vehicle. Dealers will replace the coupler at no charge.

    Product
    FOREST RIVER — 2022 FOREST RIVER XLR TOYHAULER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V144000·2022-03-11

    Keystone Travel Trailers Recalled for Faulty Wiring Disabling Safety Alarms

    Keystone is recalling 2021-2022 Sprinter and Bullet models plus multiple 2022 travel trailer and fifth-wheel variants due to faulty solar controller wiring that can disable carbon monoxide and propane gas detectors.

    Product
    KEYSTONE — 2022 KEYSTONE SPRINTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V149000·2022-03-11

    2022 Ford Escape High Voltage Battery Failure Causes Drive Power Loss

    The high voltage battery in 2021-2022 Ford Escape and 2022 Lincoln Corsair hybrid vehicles may fail, causing sudden loss of drive power and increasing crash risk.

    Product
    FORD — 2022 FORD ESCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V151000·2022-03-11

    2021-2022 Ford Edge Rearview Camera Software Error Causes Display Failure

    Ford is recalling 2021-2022 Edge vehicles with a software error that may cause the rearview camera to display a blank or distorted image. This reduces driver visibility behind the vehicle, increasing crash risk.

    Product
    FORD — 2021 FORD EDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V145000·2022-03-11

    2020-2022 Ford F-59 Steering Shaft Bolt May Loosen, Increasing Crash Risk

    The bolt securing the intermediate steering shaft to the steering gear box may become loose, potentially causing loss of steering control and increased crash risk. Ford is replacing the bolts for free.

    Product
    FORD — 2022 FORD F-59
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0815-2022·2022-03-09

    Vadilal Quick Treat Custard Apple Pulp Recalled for Salmonella

    Vadilal Industries is recalling Quick Treat Custard Apple Pulp (1kg packages, UPC 8901777282168) due to potential Salmonella contamination. Approximately 997 cases were distributed nationwide to retail stores.

    Product
    Vadilal Quick Treat Custard Apple Pulp Net Wt, 1kg/35.27-oz. Product code FPEP44302 UPC:8901777282168 Best Before September 2023
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0806-2022·2022-03-09

    Whole Foods Market Vanilla Shortbread Cookies Recalled Due to Undeclared Egg

    Whole Foods Market Vanilla Shortbread Cookies are recalled due to undeclared egg allergen. The 23 units distributed in Washington D.C. with pack date 1/20/22 may pose serious risk to consumers with egg allergies.

    Product
    Whole Foods Market Vanilla Short Bread Cookies packaged in clear plastic container with a white scale label applied PLU 66705
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0663-2022·2022-03-09

    Philips Respironics V60 Plus Ventilators with Defective Adhesive Recalled

    Respironics California is recalling 294 V60 Plus ventilators assembled with expired adhesive. The adhesive may fail, causing the bracket to loosen and damage capacitors, potentially stopping ventilation delivery.

    Product
    Philips Respironics V60 Plus Ventilator Part Number 1138747
    Category
    Medical Device
    Distribution
    13 states
  • SevereFDA (Devices)·Z-0662-2022·2022-03-09

    Philips V60 Ventilator Recall: Expired Adhesive May Cause Device Failure

    A limited number of Philips Respironics V60 ventilators were assembled with expired adhesive. If the adhesive fails, the ventilator could stop providing ventilation.

    Product
    Philips Respironics V60 Ventilator Part Number 1053617
    Category
    Medical Device
    Distribution
    13 states
  • SevereFDA (Devices)·Z-0659-2022·2022-03-09

    COVID-19 Rapid Test Kits Recalled for Risk of False Positive Results

    Celltrion DiaTrust COVID-19 Ag Rapid Test kits from lot COVGCCM0008 are being recalled due to reports of false positive results. The affected 243 kits were distributed to six states before the recall.

    Product
    Celltrion DiaTrust COVID-19 Ag Rapid Test, Reference No. CT-P60 D-2 02
    Category
    Medical Device
    Distribution
    6 states
  • SevereFDA (Food)·F-0813-2022·2022-03-09

    Enoki Mushrooms Recalled Due to Listeria monocytogenes Contamination Risk

    GOLDEN MEDAL MUSHROOM INC is recalling Xuerong brand enoki mushrooms contaminated with Listeria monocytogenes. The affected product was distributed in California, Texas, and Illinois.

    Product
    Enoki Mushrooms, brand Xuerong, net wt. 150 g/ 5.25200g/7.05-ounce packages, UPC 6953150110157. 34 0er carton.
    Category
    Food
    Distribution
    3 states