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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19001–19025 of 90006

  • HighNHTSA·23V437000·2023-06-21

    2023 Volkswagen GTI and Golf R suspension strut mount defect

    Volkswagen is recalling certain 2023 GTI and Golf R vehicles due to deformed suspension strut mounts that may loosen and cause steering instability. Dealers will replace affected components at no cost.

    Product
    VOLKSWAGEN — VOLKSWAGEN GTI, GOLF R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1920-2023·2023-06-21

    Aspira Drainage Catheter Insertion Tray valve assembly may fail to open

    Merit Medical Systems is recalling certain Aspira Drainage Catheter Insertion Trays (Model 15.5F) due to a potential valve assembly defect that could prevent fluid drainage. No injuries have been reported.

    Product
    Aspira Drainage Catheter Insertion Tray 15.5F, REF: ASP-15-5, STERILE EO, Rx Only *EU Distribution only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0872-2023·2023-06-21

    Hand Sanitizer Recalled Due to Manufacturing Deficiency and Methanol Risk

    Jarman's Midwest Cleaning Systems recalled 1,276 gallons of isopropyl alcohol hand sanitizer nationwide due to manufacturing deficiencies and potential methanol contamination risk found at the production site.

    Product
    Isopropyl Alcohol Antiseptic 75%, Topical Solution, Hand Sanitizer Non-sterile Solution, Volume: 3.785 L, plastic gallon bottle, MCS Midwest Cleaning Solutions, 404 Noid Rd., Canton, SD 57013. NDC: 74663-002-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0986-2023·2023-06-21

    Texas Pete Buffalo Wing Sauce recalled for undeclared soy allergen

    T.W. Garner Food Co. is recalling Texas Pete Buffalo Wing Sauce due to undeclared soybean oil and soy lecithin. The product was distributed to 14 states.

    Product
    Texas Pete BUFFALO Wing Sauce 12 FL OZ - 355 mL TW GARNER FOOD CO. WINSTON-SALEM, NC 27105 UPC 0 75500 10011 6
    Category
    Food
    Distribution
    14 states
  • SevereUSDA FSIS·025-2023·2023-06-20

    USDA Recalls Ineligible Imported Ready-to-Eat Pork Rind Product

    Distribuidora El Paisano Import is recalling 1,715 pounds of TorTrix Con Chicharrón pork rinds imported from Guatemala, a country ineligible to export meat to the U.S.

    Product
    Distribuidora El Paisano Import, LLC, Recalls Ineligible Ready-To-Eat Pork Rind Product Imported from Guatemala
    Category
    Food
    Distribution
    4 states
  • SevereUSDA FSIS·026-2023·2023-06-20

    BCI Foods Recalls Chicken Noodle Soup for Import Violation

    BCI Foods Inc. is recalling approximately 13,561 pounds of chicken noodle soup products that were not presented for FSIS import reinspection.

    Product
    BCI Foods Inc. Recalls Chicken Noodle Soup Products Produced Without Benefit of Import Reinspection
    Category
    Food
    Distribution
    4 states
  • HighNHTSA·23V434000·2023-06-19

    2023 Tesla Model 3 and Model Y Battery Disconnect Defect Recall

    Tesla is recalling 26 Model 3 and Model Y vehicles from 2023 because the pyrotechnic battery disconnect may fail to isolate the high-voltage battery after a crash, creating a risk of electrical shock.

    Product
    TESLA — TESLA MODEL Y, MODEL 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V433000·2023-06-16

    Altec Recalls L and LR Series Aerial Devices for Hydraulic Hose Defect

    Altec is recalling 1999-2022 L and LR Series aerial devices because a hydraulic hose may fail, causing the platform or load to move unexpectedly.

    Product
    ALTEC — ALTEC LR SERIES AERIAL DEVICE, L SERIES AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V430000·2023-06-15

    2023 Honda Civic recalled for brake modulator fluid leak

    Honda recalls 2023 Civic vehicles with a defective brake modulator that may leak fluid, potentially causing unintended vehicle movement or increased brake pedal travel.

    Product
    HONDA — HONDA, ACURA ACCORD, INTEGRA, RDX, CIVIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23222·2023-06-15

    Oceanic SCUBA Buoyancy Compensating Devices Recalled for Drowning Hazard

    Huish Outdoors is recalling Oceanic brand SCUBA diving buoyancy compensating devices because the weight pocket handle can break during use, preventing divers from dumping weight in an emergency to surface safely. No injuries have been reported, but 73 broken handles have been documented.

    Product
    SCUBA Diving Buoyancy Compensating Devices OceanPro, Excursion, Hera
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V431000·2023-06-15

    Honda Odyssey, Pilot, Passport Rearview Camera Display Failure Recall

    A faulty MOST cable connector in certain 2018-2023 Honda Odyssey, Pilot, and Passport vehicles may prevent the rearview camera image from displaying, reducing rear visibility and increasing crash risk.

    Product
    HONDA — HONDA PASSPORT, ODYSSEY, PILOT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V432000·2023-06-15

    2023 Toyota Camry and Camry Hybrid: Loose Wheel Lug Nuts Risk Detachment

    Toyota is recalling 298 2023 Camry and Camry Hybrid vehicles because lug nuts attaching wheels may be loose, risking wheel detachment and loss of vehicle control. Owners are advised not to drive until dealers repair the issue.

    Product
    TOYOTA — TOYOTA CAMRY HYBRID, CAMRY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V428000·2023-06-15

    2023 Grand Design Momentum Toy Hauler Recall: Incorrect Cargo Capacity Label

    Grand Design RV is recalling certain 2023 Momentum toy haulers due to an incorrect Cargo Carrying Capacity label. The mislabeled weight information can lead to vehicle overload, increasing crash risk.

    Product
    GRAND DESIGN — GRAND DESIGN MOMENTUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23223·2023-06-15

    Trek Bicycles with Promax Hydraulic Disc Brakes Recalled for Crash Hazard

    Trek Bicycle Corp. is recalling about 96,900 bicycles equipped with Promax hydraulic disc brakes because the brake hose can detach from the brake lever, posing a crash hazard. Trek has received 195 reports of this issue with no injuries reported.

    Product
    Promax hydraulic disc brakes sold on Trek bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1666-2023·2023-06-14

    StealthStation Cranial Software displays inaccurate navigation during brain surgery

    A software anomaly in Medtronic's StealthStation Cranial Software may cause inaccurate surgical navigation during brain procedures. This can result in unintended tissue damage and prolonged surgery.

    Product
    StealthStation Cranial Software, Model: 9735585, used with StealthStation S7/i7 systems
    Category
    Medical Device
    Distribution
    1 state
  • CriticalFDA (Food)·F-0983-2023·2023-06-14

    Cookies Recalled for Undeclared Soy and Wheat Allergens

    TETAS Mireya, SABOR Galleta Oreo cookies are being recalled due to undeclared soy and wheat allergens. Consumers with soy or wheat allergies should not consume this product.

    Product
    TETAS Mireya, SABOR Galleta Oreo
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Devices)·Z-1650-2023·2023-06-14

    Philips Trilogy and LifeVent ventilator models recalled for flow sensor debris

    Environmental debris accumulation may block flow sensors in Philips ventilators, potentially preventing accurate pressure and flow delivery to patients.

    Product
    Trilogy Evo O2 and LifeVent EVO2, Model Numbers DS2100X11B, IN2100X15B, IN2100X19, FX2100X15B, LA2100X15B, IA2100X15B, FP2100X10, FR2100X14B, ND2100X15B, IT2100X21B, ES2100X15B, DE2100X13B, EU2100X15B, EU2100X19, EE2100X15B, and SP2100X26B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0976-2023·2023-06-14

    Tastykake Chocolate Kandy Kakes recalled for undeclared peanuts

    Tastykake Chocolate Kandy Kakes are being recalled due to undeclared peanuts. The product poses a serious risk to individuals with peanut allergies.

    Product
    Tastykake Chocolate Kandy Kakes NET WT 8 OZ (227g) 6-1.3 OZ (38g) PKGS TASTY BAKING COMPANY, PHILADELPHIA, PA 19112 UPC 0 25600 00225 4
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Devices)·Z-1633-2023·2023-06-14

    FDA Recalls Walnut Wearable Smart Thermometer Due to Reported Skin Burns

    BearCare's Walnut Wearable Smart Thermometer (Model WT20) is being recalled due to reports of skin burns in children ages 0-6. The device was distributed nationwide; 1818 units were affected.

    Product
    Walnut Wearable Smart Thermometer, intended for continuous chest temperature monitoring of children ages 0-6 years in non-emergency medical situations, Model Number WT20
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1649-2023·2023-06-14

    Philips Respironics Ventilators Recalled for Flow Sensor Debris Accumulation

    Philips Respironics recalled approximately 57,395 ventilators due to environmental debris potentially accumulating on the flow sensor, which may prevent accurate delivery of pressure and volume to patients, risking hypoxemia.

    Product
    Trilogy Evo, Garbin Evo, and Aeris EVO, Model Numbers DS2110X11B, IN2110X15B, JP2110X16B, AU2110X15B, LA2110X15B, CA2110X12B, BR2110X18B, KR2110X15B, IA2110X15B, FP2110X10, FR2110X14B, ND2110X15B, IT2110X21B, ES2110X15B, DE2110X13B, BL2110X15B, GB2110X15B, EU2110X15B…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0980-2023·2023-06-14

    TETAS Mireya candy recalled for undeclared soy and walnut allergens

    DIBE LLC is recalling TETAS Mireya candy due to undeclared soy and walnut allergens. Consumers with allergies to these ingredients should not consume the product.

    Product
    TETAS Mireya, SABOR Ferrero
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0977-2023·2023-06-14

    Onion Powder Premium Recalled for Potential Salmonella Contamination

    Olam Food Ingredients is recalling Onion Powder Premium sold in bulk fiber bags due to potential Salmonella contamination. Affected product was distributed to Canada, Arkansas, and Illinois.

    Product
    Onion Powder Premium, 44.9 and 50 lb. fiber bags sold as bulk ingredient
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0979-2023·2023-06-14

    TETAS Mireya Galleta Maria Cookies Recalled for Undeclared Soy and Wheat

    DIBE LLC is recalling TETAS Mireya SABOR Galleta Maria cookies due to undeclared soy and wheat allergens. Consumers with allergies to these ingredients should not consume the product.

    Product
    TETAS Mireya, SABOR Galleta Maria
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1630-2023·2023-06-14

    StealthStation Cranial Software Depth Gauge Synchronization Failure Risk

    A software anomaly in StealthStation Cranial Software causes depth gauge displays to lose synchronization during cranial biopsy procedures, risking inaccurate surgical guidance and tissue injury.

    Product
    StealthStation Cranial Software, Models: 9735585, 9735586 (kit), 9735587 (kit), used with StealthStation S7/i7 systems
    Category
    Medical Device
    Distribution
    Distributed nationwide