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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10951–10975 of 36632

  • SevereNHTSA·20V463000·2020-08-07

    American Hauler Recalls 2018 Trailers Due to Axle Weld Failures

    American Hauler is recalling 2018 Air-Lite, Arrow, Falcon/XC, and Night Hawk trailers because spindle weld failures on the axles may increase the risk of a crash or injury.

    Product
    AMERICAN HAULER — AMERICAN HAULER ARROW, NIGHT HAWK, AIR-LITE, FALCON/XC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V466000·2020-08-07

    2017-2021 Freightliner Business Class M2 trucks recalled for electrical harness defect

    Daimler Trucks North America is recalling certain 2017-2021 Freightliner Business Class M2 trucks because the engine harness may contact and chafe, potentially short-circuiting and causing engine stall during operation.

    Product
    FREIGHTLINER — FREIGHTLINER BUSINESS CLASS M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2729-2020·2020-08-05

    Teleflex Medical Recalls Rusch Greenlite Laryngoscopes Due to Welded Joint Breakage

    Teleflex Medical is recalling Rusch Greenlite laryngoscopes because the welded joint may break. The recall covers 20,600 units distributed nationwide.

    Product
    Rusch Greenlite Product Code: 004551002 GTIN: 14026704663115 (each) - Product Usage: The laryngoscope is a device intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2738-2020·2020-08-05

    Hill-Rom Recalls 1,033 Centralia Smart+ Beds Due to Screw Defect

    Hill-Rom is recalling 1,033 Centralia Smart+ Beds because screws may not meet tensile strength requirements, posing a risk of serious injury.

    Product
    Centrella Smart+ Bed, Catalog No. P7900 - Product Usage: intended to be used to treat or prevent pulmonary or other complications associated with immobility; to treat or prevent pressure ulcers; or for any other use where medical benefits may be derived from either Continuous…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2737-2020·2020-08-05

    Hill-Rom Recalls Progressa Beds Due to Screw Tensile Strength Defect

    Hill-Rom is recalling 257 Progressa Beds because screws may not meet tensile strength requirements, posing a risk of serious injury to patients or users.

    Product
    Progressa Bed, Catalog No. P7500 - Product Usage: intended to be used to treat or prevent pulmonary or other complications associated with immobility; to treat or prevent pressure ulcers; or for any other use where medical benefits may be derived from either Continuous Lateral…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V456000·2020-08-05

    Blue Bird Recalls 2021 School Buses Due to Steering Wheel Nut Issue

    Blue Bird is recalling 2021 Vision and All American school buses because the steering wheel nut may not be tightened properly, risking loss of control.

    Product
    BLUE BIRD — BLUE BIRD VISION SCHOOL BUS, ALL AMERICAN SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V455000·2020-08-05

    Blue Bird Recalls 2021 Transit Buses Due to Steering Wheel Nut Issue

    Blue Bird is recalling 2021 Vision and All American transit buses because the steering wheel nut may not be properly tightened, risking loss of vehicle control.

    Product
    BLUE BIRD — BLUE BIRD VISION TRANSIT BUS, ALL AMERICAN TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1412-2020·2020-08-05

    Saniderm Hand Sanitizer Recalled for Undeclared Methanol and Low Ethanol

    Polarized LLC is recalling Saniderm Advanced Hand Sanitizer because it contains undeclared methanol and less ethanol than labeled.

    Product
    Saniderm ADVANCED HAND SANITIZER, 70% Alcohol Content, 1 Liter bottles, Distributed by Polarized, LLC, Produced by Eskbiochem SA de CV, Mexico Japon 50, Celaya, Gto., Mexico, 38010. UPC 8 60003 63391 5.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2742-2020·2020-08-05

    OrthoPediatrics Recalls Spine Rods Due to Potential Fracture Risk

    OrthoPediatrics Corp is recalling 73 units of 6.0MM spine rods because incorrect laser etching may compromise strength and lead to unintended fracture.

    Product
    Orthopedics 6.0MM ROD, COCR, SINGLE HEX, 500MM LENGTH-The RESPONSE" 5.5/6.0 Spine System is intended for immobilization and stabilization of the posterior, non-cervical spine in skeletally mature patients as an adjunct to fusion for the following indications: degenerative disc…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1046-2020·2020-08-05

    Winter Gardens Spinach Artichoke Dip Recalled for Undeclared Egg Allergen

    Winter Gardens Quality Foods is recalling Spinach Artichoke Dip due to undeclared egg. The product was distributed to Whole Foods Market in the Mid-Atlantic region.

    Product
    Whole Foods Spinach Artichoke Dip ,4-12 oz containers, Lot # 248 Manufactured on 7/8/2020 Use By: 07/26/2020
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Drugs)·D-1427-2020·2020-08-05

    MasterPharm Recalls Progesterone Capsules Due to Processing Control Deficiencies

    MasterPharm LLC is recalling 600 capsules of Progesterone (Modified Release) 150 mg due to a lack of processing controls.

    Product
    Progesterone (Modified Release) 150 mg Capsule, 90 capsules per bottle, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1407-2020·2020-08-05

    Saniderm Hand Sanitizer Recalled for Undeclared Methanol Contamination

    UVT INC is recalling Saniderm Advanced Hand Sanitizer because it contains undeclared methanol. The product was distributed nationwide in the USA.

    Product
    Saniderm ADVANCED HAND SANITIZER, 70% Alcohol Content, 1 Liter bottles, Distributed by Polarized, LLC, Produced by Eskbiochem SA de CV, Mexico Japon 50, Celaya, Gto., Mexico, 38010. UPC 8 60003 63391 5.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V459000·2020-08-05

    Kia Recalls 2019 Forte Vehicles Due to Axle Driveshaft Defect

    Kia is recalling 2019 Forte vehicles because the left front axle driveshaft may not have been heat-treated, which can cause it to break and increase crash risk.

    Product
    KIA — KIA FORTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1031-2020·2020-08-05

    Greenhead Lobster Products Recalls Fresh and Frozen Lobster Meat

    Greenhead Lobster Products is recalling fresh and frozen lobster meat products due to potential contamination with Listeria monocytogenes.

    Product
    1. FRESH CLAW AND KNUCKLE MEAT, 1 and 2 lbs. 2. FRESH CLAW, KNUCKLE, AND TAIL MEAT, 1 and 2 lbs 3. FROZEN CLAW AND KNUCKLE MEAT, 2 lb
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Devices)·Z-2725-2020·2020-08-05

    Medline Recalls ClearPro Trach T-Piece Closed Suction Catheters

    Medline is recalling 680 units of ClearPro Trach T-Piece Closed Suction Catheters because the catheter may come apart from the device assembly during use.

    Product
    ClearPro Trach T-Piece Closed Suction Catheter, Model DYNCPTP14T, 14 Fr 12.5 IN FOR TRACHEOSTOMY TUBE - Product Usage: Catheters are intended for endotracheal suction of adult patients with artificial airways. Single use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V447000·2020-07-31

    Hyundai Recalls 2020 Genesis G70 for Steering Locking Risk

    Hyundai is recalling 2020 Genesis G70 vehicles because a steering component may be defective, potentially causing the steering to lock or become difficult to operate while driving.

    Product
    HYUNDAI — HYUNDAI GENESIS G70
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·018-2020·2020-07-30

    JBS Recalls Raw Boneless Beef Products Distributed Without Import Re-inspection

    JBS Food Canada ULC is recalling approximately 38,406 pounds of raw boneless beef head meat products that were imported into the United States without undergoing required FSIS import re-inspection.

    Product
    Balter Meat Company — JBS Food Canada ULC Recalls Raw Boneless Beef Products Distributed without Benefit of Import Re-inspection
    Category
    Food
    Distribution
    4 states
  • SevereNHTSA·20E052000·2020-07-30

    ZF Recalls Air Bag Crash Sensors in Chrysler and Volkswagen Vehicles

    ZF is recalling air bag crash sensors in 2019 Chrysler Jeep Cherokee and 2018 Volkswagen Atlas vehicles due to manufacturing defects that may delay or prevent air bag deployment.

    Product
    AIR BAGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1408-2020·2020-07-29

    Mystic Shield Hand Sanitizer Recalled for Undeclared Methanol

    Transliquid Technologies is recalling Mystic Shield hand sanitizer bottles due to the presence of undeclared methanol.

    Product
    Mystic Shield PROTECTION, ALCOHOL ANTISEPTIC 70%, Topical Solution, Antiseptic Hand Rub, Non-sterile Solution, Extra strength Formula*, 8.45 fl. oz. (250 ml) bottle, Labeled with green or blue labels, Manufactured by Mystic Intl S.A. de C.V. UPC barcode: 7 87790 33952 6
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2667-2020·2020-07-29

    Becton Dickinson Recalls SafeStep Huber Needle Sets Due to Tubing Cracks

    Becton Dickinson is recalling SafeStep Huber Needle Sets because tubing may crack, risking chemical exposure, blood loss, or infection.

    Product
    SafeStep Huber Needle Set with GuardIVa Antimicrobial Hemostatic Dressing; Catalog Number CPA00040 (UDI 00801741143892)
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2663-2020·2020-07-29

    Becton Dickinson Recalls PowerLoc MAX Infusion Sets Due to Tubing Cracks

    Becton Dickinson is recalling PowerLoc MAX infusion sets because tubing may crack, risking leakage of chemicals or biohazard materials.

    Product
    PowerLoc MAX Power Injectable Infusion Set with GuardIVa Antimicrobial Hemostatic Dressing Port Access Kit; Catalog Numbers 2132010G (UDI 00801741095504), 2132015G (UDI 00801741095511), 2141910G (UDI 00801741095542), 2142010G (UDI 00801741085680), 2142015G (UDI 00801741085680)…
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2668-2020·2020-07-29

    Becton Dickinson SafeStep Huber Needle Set Recall for Tubing Cracks

    Becton Dickinson is recalling SafeStep Huber Needle Sets with GuardIVa Antimicrobial Hemostatic Dressing Port Access Kits due to potential tubing cracks that may cause leakage.

    Product
    SafeStep Huber Needle Set with GuardIVa Antimicrobial Hemostatic Dressing Port Access Kit; Catalog Numbers PA-0031G (UDI 00801741085666), PA-0031YNG (UDI 00801741085673), PA-0032G (UDI 00801741087639), PA-0033G (UDI 00801741096433)
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2665-2020·2020-07-29

    Becton Dickinson Recalls SafeStep Huber Needle Sets Due to Tubing Cracks

    Becton Dickinson is recalling SafeStep Huber Needle Sets because tubing may crack, risking leakage of chemicals or blood.

    Product
    SafeStep Huber Needle Set myPICK Port Access Kit; Catalog Numbers CPA00020A (UDI 00801741129827), CPA00042A (UDI 00801741182969), CPA00049 (UDI 00801741175695)
    Category
    Medical Device
    Distribution
    0 states