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

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

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

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

Clear filters

9076–9100 of 36629

  • SevereFDA (Devices)·Z-2480-2021·2021-09-29

    Ultrasound Gels and Lotions Recalled Due to Bacterial Contamination

    Eco-Med Pharmaceutical, Inc. is recalling ultrasound gels and lotions that may contain bacterial contamination. Products were distributed nationally and internationally.

    Product
    EcoGel 100 Imaging Gel, EcoGel 200 MultiPurpose Gel (Blue), EcoGel 200 MultiPurpose Gel (CLEAR), and EcoLotion Transmission Lotion 1) 100, 200 gel Intended for use in acoustic coupling of ultrasound transducer to tissue 2) Lotion Ecolotion transmission and massage lotion is in
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2469-2021·2021-09-29

    Multiple Ultrasound Gel Products Recalled for Potential Bacterial Contamination

    Ultrasound gels sold under multiple brand names have been recalled due to potential bacterial contamination. Approximately 100,114 units distributed nationwide between August 2018 and August 2021 are affected.

    Product
    Ultrasound Gel labeled under the following brand names: MediChoice Ultrasound Gel, Athena Liquasonic Ultrasound Gel, Eco-Med EcoGel Ultrasound Gel, MAC Medical Supply Ultrasound Gel, Eco-Med EcoGel 200 Blue High Velocity Ultrasound Gel, Eco-Med EcoGel 200 Multi-Purpose Ultrasoun
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1006-2021·2021-09-29

    Golden Natural Product Dried Apricots Recalled for Undeclared Sulfites

    Golden Natural Product Inc. brand Dried Apricot Subkhon products (with bone and jumbo varieties) are being recalled because they contain high levels of undeclared sulfites. The affected products have lot number GC005 and expiration date 2023.

    Product
    Golden Natural Product Inc. brand Dried Apricot Subkhon with Bone, Net Wt. 16 oz (1 lb) 454 g; and Golden Natural Product Inc. brand Dried Apricot Subkhon Jumbo, Net Wt. 16 oz (1 lb) 454 g Manufactured and Packed by: Gardencells LLC, Urgut, Samarkand region Republic of Uzbekist
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1008-2021·2021-09-29

    Kroger Kale Bags Recalled for Potential Listeria Contamination

    The Kroger Co. is recalling Kroger Kale Bags (16 oz) due to potential contamination with Listeria Monocytogenes. The affected product was distributed to retail locations in seven states.

    Product
    Kroger Kale Bag 16oz plastic bag 8 packages per case
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0827-2021·2021-09-29

    Arformoterol Tartrate Inhalation Solution Recall Due to Sterility Assurance

    Glenmark Pharmaceuticals is recalling Arformoterol Tartrate Inhalation Solution 15 mcg/2 mL nationwide because the manufacturer lacks assurance of sterility for affected lots.

    Product
    Arformoterol Tartrate Inhalation Solution 15 mcg*/2 mL For Oral Inhalation Only Rx Only Manufactured by: Glenmark Pharmaceuticals Inc., USA Monroe, NC 28110 Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ 07430 a) 60x2 mL Sterile Unit-Dose Vials NDC 68462-833-65;
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0988-2021·2021-09-29

    Joy Coriander Chutney Recalled for Undeclared Sulfites

    Joy Coriander Chutney (8 oz, best by 07/30/22) is being recalled because it contains high levels of undeclared sulfites. Consumers with sulfite sensitivity should not consume this product.

    Product
    2. "***JOY***Coriander Chutney***NET WT 8 OZ (228g)***07 28 BEST BY 073022***INGREDIENTS: CORIANDER, GREEN CHILLIES, COCONUT, SUGAR, SALT, SPICES, VINEGAR, STABILIZERS (GUAR, TRAGAGANTH AND XANTHAN), CITIRC ACID, SODIUM BENZOATE AS PRESERVATIVE & ARTIFICIAL COLORS (FD&C BLUE 1 &
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0819-2021·2021-09-29

    X Rated Honey For Men Recalled for Undisclosed Tadalafil

    Phe Inc is recalling X Rated Honey For Men packets nationwide because the product contains Tadalafil and was marketed without FDA approval. Consumers should stop use immediately.

    Product
    X RATED HONEY FOR MEN, packaged in 15g packets, 4 packets per box, UPC 6 13682 41232 2
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·035-2021·2021-09-28

    Espi's Recalls Frozen Chicken and Pork Hot Dogs Due to Listeria

    Espi's Sausage and Tocino Co. is recalling frozen ready-to-eat chicken and pork hot dogs due to possible Listeria monocytogenes contamination.

    Product
    Espi's Sausage and Tocino Co. — Espi’s Sausage and Tocino Co. Recalls Ready-to-Eat Chicken and Pork Hot Dog Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·21V753000·2021-09-28

    Tiffin Wayfarer RV Water Tank Mounting Defect Increases Crash Risk

    Tiffin Motorhomes is recalling 2018-2022 Wayfarer RVs because the rear water tank mounting bolts can fail, causing the tank to fall onto the exhaust pipe. This affects vehicle stability and increases crash risk.

    Product
    TIFFIN — TIFFIN WAYFARER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V752000·2021-09-27

    Spartan K3 and K4 Recalled for Power Steering Pump Defect

    Shyft Group is recalling 2020-2022 Spartan K3 and K4 RVs because a machining defect may cause the power steering pump shaft seal to break, resulting in a loss of power steering assist.

    Product
    SPARTAN — SPARTAN K4, K3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V617000·2021-09-27

    Toyota Recalls 2019-2020 Yaris Models for Fuel Pump Defect

    Toyota is recalling 2019-2020 Yaris vehicles because a fuel pump impeller may crack, potentially causing engine stalls and increasing crash risk.

    Product
    TOYOTA — TOYOTA YARIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·034-2021·2021-09-26

    Nestle Recalls DiGiorno Pepperoni Pizza Due to Undeclared Soy Allergen

    Nestle is recalling approximately 27,872 pounds of frozen DiGiorno Crispy Pan Crust Pepperoni Pizza because some cartons contain undeclared soy protein.

    Product
    Nestlé USA Inc. Recalls Frozen DiGiorno Crispy Pan Crust Pepperoni Pizza Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·033-2021·2021-09-25

    Ajinomoto Recalls Raw Frozen Chicken Potstickers Due to Plastic Contamination

    Ajinomoto Foods North America is recalling raw, frozen chicken and vegetable potstickers that may contain clear flexible and hard plastic.

    Product
    Ajinomoto Foods North America Inc Recalls Raw, Frozen Chicken and Vegetable Potsticker Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V748000·2021-09-24

    MCI Motorcoaches Recalled for Main Distribution Panel Fire Risk

    Motor Coach Industries is recalling specific 2017-2021 motorcoaches because a circuit board in the battery compartment may fail, potentially causing a fire or unexpected shutdown.

    Product
    MCI — MCI D45 CRT LE, D4000ISTV, D4500, D4505
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·21198·2021-09-23

    Boppy Newborn Loungers Recalled After Eight Infant Deaths

    The Boppy Company is recalling approximately 3.3 million Boppy newborn loungers due to suffocation risk. Eight infant deaths have been reported associated with the product.

    Product
    Boppy Original Newborn Loungers, Boppy Preferred Newborn Loungers and Pottery Barn Kids Boppy Newborn Loungers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V733000·2021-09-23

    DRV Recalls 2018-2021 Elite and Mobile Suites Due to Brake Caliper Defect

    DRV Suites is recalling 2018-2021 Elite and Mobile Suites because brake caliper clips may bend, causing the caliper to unseat and increasing crash risk.

    Product
    DRV — DRV ELITE SUITE, MOBILE SUITE, MOBILE SUITES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V736000·2021-09-23

    Altec Recalls 2011-2016 Aerial Devices Due to Mounting Frame Cracks

    Altec is recalling 2011-2016 AT200A aerial devices because cracks in the mounting frame legs may cause the side plate to break, increasing injury risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V740000·2021-09-23

    Braun Recalls Demers Ambulances Due to Fire Risk from Damaged Wires

    Braun Ambulances is recalling 2020-2021 Demers MXP153 vehicles because damaged electrical wires and oxygen tubes may increase fire risk.

    Product
    DEMERS AMBULANCES — DEMERS AMBULANCES MXP153 FORD F-SERIES, MXP153 DODGE RAM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V732000·2021-09-23

    Volkswagen Recalls 2018 Tiguan Vehicles Due to Roof Reinforcement Defect

    Volkswagen is recalling 2018 Tiguan vehicles because an incorrect roof reinforcement assembly may have been installed during prior repairs, potentially compromising structural integrity and airbag deployment.

    Product
    VOLKSWAGEN — VOLKSWAGEN TIGUAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V742000·2021-09-23

    2022 Nissan Pathfinder: Third-Row Headrests May Detach or Move

    Nissan is recalling 2022 Pathfinder vehicles because the third-row headrests may move or detach due to improper welds or misaligned components. Detached headrests could fail to restrain occupants in a crash, increasing injury risk.

    Product
    NISSAN — NISSAN PATHFINDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0804-2021·2021-09-22

    Spironolactone Ophthalmic Solution Recalled for Lack of Sterility Assurance

    Greenpark Compounding Pharmacy is recalling Spironolactone Ophthalmic Solution 0.005 mg/mL due to lack of assurance of sterility. The 15 mL bottles were distributed nationwide.

    Product
    Spironolactone Ophthalmic Solution 0.005 mg/mL, 15 mL bottles, Rx only, Greenpark Compounding Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2428-2021·2021-09-22

    Angiographic Catheter Recall: Cordis SUPER TORQUE Entrapment and Dislodgement Risk

    Cordis is recalling its SUPER TORQUE MB Angiographic Catheter worldwide because it may become entrapped between endovascular devices and the vessel wall. This entrapment can cause marker band movement or dislodgement.

    Product
    Cordis 5F UNIVERSAL FLUSH F4 SUPER TORQUE MB, SPECIAL, Angiographic Catheter, REF SRD6785MB
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2429-2021·2021-09-22

    Cordis Angiographic Catheter Recall Due to Potential Marker Band Dislodgement

    Cordis is recalling approximately 1,610 SUPER TORQUE PIG PIGTAIL SPECIAL angiographic catheters worldwide because the device can become entrapped between endovascular devices and the vessel wall, potentially causing marker band movement or dislodgement.

    Product
    Cordis 5F SUPER TORQUE PIG PIGTAIL SPECIAL, Angiographic Catheter, REF SRD7040MB
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0805-2021·2021-09-22

    AMINOSYN II 15% Amino Acid Injection Recalled for Particulate Matter

    ICU Medical Inc is recalling AMINOSYN II 15% An Amino Acid Injection due to the presence of particulate matter including fibers, hair, and proteinaceous material found in retained samples.

    Product
    AMINOSYN II 15% An Amino Acid Injection, Sulfite-Free, 2000 mL in flexible containers, Rx ONLY, Hospira, Inc., Lake Forest, IL 60045. NDC 0409-7171-17
    Category
    Drug
    Distribution
    Distributed nationwide