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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20151–20175 of 90018

  • HighFDA (Drugs)·D-0492-2023·2023-04-12

    Doxazosin 2 mg tablets recalled for manufacturing practice deviations

    RemedyRepack Inc. is voluntarily recalling Doxazosin 2 mg tablets distributed nationwide due to current Good Manufacturing Practice (cGMP) deviations. The recall affects 30-count and 90-count bottles.

    Product
    Doxazosin 2 mg tablets, packaged in a) 30-count (NDC 70518-1560-00) and b) 90-count bottles (NDC 70518-1560-01), Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0507-2023·2023-04-12

    Alprazolam 0.5 mg tablets recalled due to manufacturing contamination

    Direct Rx is recalling Alprazolam 0.5 mg tablets (Lot 11AP2219, expires 4/30/23) nationwide due to potential cross-contamination concerns at the manufacturer. No illnesses have been reported.

    Product
    Alprazolam C-IV, 0.5 mg, 30 Tabs per bottle, Rx only, Packaged and Distributed By: Direct Rx Dawsonville, GA 30534, NDC 72189-0240-30.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1328-2023·2023-04-12

    Medtronic Grafton Matrix surgical strips: potential sterile barrier packaging defects

    Medtronic is recalling Grafton Matrix Strips due to potential defects in the sterile packaging barrier. Non-conforming packaging could allow sterile barrier compromise in this surgical implant product.

    Product
    Medtronic Grafton Matrix Strips: a) DBM S42275 8MMX1CMX10CM 2EA MATRIX STRPS, REF S42275; b) DBM S42280 8MMX1CMX20CM 2EA MATRX STRPS, REF S42280; c) DBM T42275 8MMX1CMX10CM 2 EACH GRAFTON M, REF T42275; d) DBM T42275AUS 8MMX1CMX10CM 2 EA GRFTON S, REF T42275AUS; e)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0504-2023·2023-04-12

    Alprazolam 0.25mg tablets recalled for potential cross contamination

    Preferred Pharmaceuticals is recalling Alprazolam 0.25mg tablets (Lot G1822K, expiration 5/31/2023) nationwide due to potential cross contamination from manufacturing deviations. No illnesses have been reported.

    Product
    Alprazolam Tab, USP 0.25mg, (CIV), 30-count bottle, Rx Only, Preferred Pharmaceuticals, Inc. Manufactured by: Breckenridge Pharmaceuticals, Inc., Boca Raton, FL. Ins:NDC 68788-7594-3
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0520-2023·2023-04-12

    Rosuvastatin Tablets Recalled Due to Manufacturing Deviations

    Preferred Pharmaceuticals is recalling 264 bottles of Rosuvastatin Tablets 5mg nationwide due to manufacturing deviations discovered during FDA inspection. No illnesses have been reported.

    Product
    Rosuvastatin Tablets, USP, 5mg, 30-count bottle, Rx only, Manufactured: Accord Healthcare, Inc., Durham, NC 27703, NDC 68788-7971-3
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1325-2023·2023-04-12

    Medtronic Grafton Flex bone graft products recalled for packaging integrity defects

    Medtronic is recalling Grafton Flex demineralized bone matrix products due to potential packaging non-conformances that could compromise sterile barrier integrity. Approximately 2,987 units were distributed worldwide.

    Product
    Medtronic Grafton Flex: a) DBM S42090 GRAFTON 1.5CM X 1.5CM FLEX, REF S42090; b) DBM T42090 1.5CMX1.5CM FLEX GRAFTON, REF T42090; c) DBM T42090INT 1.5CMX1.5CM FLEX GRAFTON, REF T42090INT; d) DBM T42100 2.5CMX10CM FLEX GRAFTON, REF T42100; e) DBM T42100AUS 2.5CMX10CM FLEX…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1347-2023·2023-04-12

    CAPIOX FX25 Oxygenator Recalled for Potential Leaks from Improper Bonding

    Terumo Cardiovascular Systems is recalling 4,940 CAPIOX FX25 oxygenators because an arterial thermistor component may be improperly bonded to the oxygenator port, potentially causing leaks.

    Product
    CAPIOX FX25 Hollow Fiber Oxygenator, Catalog Numbers 3CX*FX25REC, 3CX*FX25RWC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1339-2023·2023-04-12

    Stryker Tourniquet Cuff May Fail to Hold Pressure During Surgery

    Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuffs may fail to achieve or hold pressure during initial surgical setup. This failure could allow blood to flow from the surgical site, potentially causing hemorrhage.

    Product
    Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 30X4,1BLA,1PRT QUICK Catalog number: 5921-030-135NS Indicated for use in surgical procedures that require the temporary occlusion of blood flow in a patient s extremities
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0525-2023·2023-04-12

    Simvastatin Tablets Recalled Due to Manufacturing Practice Deviations

    Preferred Pharmaceuticals is recalling Simvastatin 40 mg tablets nationwide due to manufacturing practice violations at the production facility. The recall is precautionary.

    Product
    Simvastatin Tablets, USP, 40 mg, Packaged as: a) 90-count bottle (NDC 68788-9868-9); b) 60-count bottle (NDC 68788-9868-6); c) 30-count bottle (NDC 68788-9868-3), Rx only, Manufactured for: Accord Healthcare, lnc., Durham, NC 27703.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1341-2023·2023-04-12

    Stryker Tourniquet Cuff Pressure Failure May Lead to Blood Loss

    Stryker's non-sterile disposable tourniquet cuff may fail to achieve or maintain proper pressure during surgical setup, potentially causing blood loss or hemorrhage. Approximately 1,979 units distributed nationwide are affected.

    Product
    Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 34X4,1BLA,1PRT QUICK Catalog number: 5921-034-135NS Indicated for use in surgical procedures that require the temporary occlusion of blood flow in a patient s extremities
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·23E031000·2023-04-11

    Meritor Recalls Front Drive Steer Axles Due to Fastener Loosening

    Meritor is recalling specific front drive steer axles because fasteners may loosen, potentially causing axle separation and loss of vehicle control.

    Product
    STEERING:CRITICAL FASTENERS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V259000·2023-04-07

    Thomas Built Buses Recall 48 School Buses for Steering Defect

    Daimler Trucks North America is recalling 48 Thomas Built Buses school buses because a missing fastener may allow the steer arm to detach, risking loss of steering control.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2 JOULEY, SAF-T-LINER C2, SAF-T-LINER MVP-EF, HDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V207000·2023-04-07

    Lightning eMotors Recalls 148 Vehicles Due to Battery Pack Defects

    Lightning eMotors is recalling 148 electric vehicles because defective battery pack welds may cause internal leaks, leading to battery failure, loss of power, or fire.

    Product
    LIGHTNING EMOTORS — LIGHTNING EMOTORS FE4-129, FT3-86, FT3-43, FE4-86
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V255000·2023-04-07

    Volvo VNR Trucks Recalled for Aggressive Adaptive Cruise Control Braking

    Volvo Trucks is recalling 2020-2023 VNR Electric vehicles equipped with Adaptive Cruise Control that can trigger aggressive braking under light load conditions, risking rear axle skidding and loss of vehicle control.

    Product
    VOLVO — VOLVO VNR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V257000·2023-04-07

    Buell Recalls 2021-2022 1190 RX and SX Motorcycles for Gear Shift Defect

    Buell Motorcycles is recalling 2021-2022 1190 RX and SX motorcycles because an improperly installed index spring may cause gear slipping or shifting failure, increasing crash risk.

    Product
    BUELL — BUELL 1190 RX HAMMERHEAD, 1190 SX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V256000·2023-04-07

    Alamo Group Recalls 2014-2019 Super Products Camel and Mud Dog Trailers

    Alamo Group is recalling 2014-2019 Super Products Camel and Mud Dog trailers because a tie rod could disconnect, allowing the water tank strap to detach and become a road hazard.

    Product
    SUPER PRODUCTS — SUPER PRODUCTS CAMEL, MUD DOG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-04072023-01·2023-04-07

    Russ' Commissary Fresh Salads Recalled Due to Possible Listeria Contamination

    The USDA FSIS issued a public health alert recalling fresh salads with chicken and ham containing lettuce due to possible Listeria monocytogenes contamination.

    Product
    Russ' Commissary — FSIS Issues Public Health Alert for Fresh Salads With Chicken and Ham Containing Lettuce Recalled by FDA for Possible Listeria Monocytogenes Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·23V254000·2023-04-07

    Starcraft Prodigy School Buses Recalled for Ceiling Panel Defect

    Forest River Bus is recalling 2019-2022 Starcraft Prodigy school buses because improperly secured ceiling panels may not protect passengers in a crash.

    Product
    STARCRAFT BUS — STARCRAFT BUS PRODIGY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V258000·2023-04-07

    2023 Subaru Ascent Tire Bead Damage Increases Crash Risk

    Subaru is recalling certain 2023 Ascent vehicles equipped with 20-inch wheels due to potential tire bead damage during manufacturing. The defect may cause sudden air pressure loss and increase crash risk.

    Product
    SUBARU — SUBARU ASCENT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V246000·2023-04-06

    Prevost Recalls 2023 X3-45 VIP Motor Coaches Due to Fire Risk

    Prevost is recalling 2023 X3-45 VIP motor coaches because a missing grommet allows electrical cables to chafe, potentially causing a short circuit and fire.

    Product
    PREVOST — PREVOST X3-45 VIP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V253000·2023-04-06

    2023 BMW X5 Head Restraints May Fail in Crash

    BMW is recalling approximately 235 certain 2023 X5 vehicles with defective second-row head restraints that may not properly restrain occupants during a crash, violating federal safety standards.

    Product
    BMW — BMW X5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23174·2023-04-06

    Mammut Avalanche Shovels Recalled for Spring Locking Mechanism Failure

    Mammut Sports Group is recalling Alugator Ride 3.0 Hoe and Alugator Ride SE avalanche shovels because the spring locking mechanism can fail during emergency excavation, posing risk of injury or death.

    Product
    Alugator Ride 3.0 Hoe and Alugator Ride SE avalanche shovels
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V245000·2023-04-06

    Prevost Recalls 2023 X3-45 Motor Coaches Due to Electrical Fire Risk

    Prevost is recalling 2023 X3-45 and X3-45 VIP motor coaches because an insufficient grommet allows electrical cables to chafe, potentially causing a short circuit and fire.

    Product
    PREVOST — PREVOST X3-45 VIP, X3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V248000·2023-04-06

    Navistar Recalls International Buses Due to HVAC Wiring Fire Risk

    Navistar is recalling 2016-2020 International and IC Bus models because an HVAC wiring terminal may overheat, increasing the risk of a fire.

    Product
    INTERNATIONAL — INTERNATIONAL, IC BUS TRANSTAR, DURASTAR, PROSTAR, LONESTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide