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.

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9026–9050 of 36629

  • SevereNHTSA·21V800000·2021-10-14

    Volvo Recalls 2001-2007 V70 and XC70 for Air Bag Inflator Defect

    Volvo is recalling 2001-2007 V70 and XC70 vehicles because the driver's air bag inflator may explode during deployment, posing a risk of serious injury or death.

    Product
    VOLVO — VOLVO V70, XC70
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·039-2021·2021-10-14

    Evans Food Group Recalls Pork Products Imported Without Inspection

    Evans Food Group is recalling pork products that were imported into the U.S. without the required re-inspection. No illnesses have been reported.

    Product
    Evans Food Group — Evans Food Group Recalls Pork Products Imported Without Benefit of Inspection
    Category
    Food
    Distribution
    6 states
  • SevereNHTSA·21V798000·2021-10-14

    RAM Pickup and Cab Chassis Trucks: Intake Heater Relay Fire Risk

    Certain 2021-2022 RAM pickup and cab chassis trucks with Cummins diesel engines may experience electrical shorts in the Intake Heater Grid Relay, causing a fire hazard. Owners should park outside until dealers inspect and repair the defect.

    Product
    RAM — RAM 2500, 4500, 3500, 5500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0009-2022·2021-10-13

    Kale Recalled for Listeria monocytogenes Contamination

    Terry and Joe Baker Farms is recalling 16 oz packages of kale sold under the Baker Farms, Kroger, and SEG Grocers brand names due to Listeria monocytogenes contamination detected during testing.

    Product
    KALE NET WT 16 OZ (1 LB) 454g Sold under the following brand names: Baker Farms 3667 Ellenton Norman Park Road, Norman Park GA 31771 UPC 8 13098 02001 6; Kroger DISTRIBUTED BY THE KROGER CO. CINCINNATI, OHIO 45202 UPC 0 11110 18170 1 & SEG Grocers DISTRIBUTED BY: SOUTHEASTERN GRO
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Drugs)·D-0002-2022·2021-10-13

    Artesunate for Injection Recalled Due to Sterility Assurance Failure

    AMIVAS (US), LLC is recalling Artesunate for Injection (110 mg/vial) because an air filter failed post-integrity testing, creating a lack of sterility assurance for the product.

    Product
    Artesunate for Injection, 110 mg/vial, packaged in a) 2x2 pack containing 2 Single-dose vials artesunate (73607-001-01) and 2 vials sterile diluent (NDC 73607-001-02) per carton (NDC 73607-001-11); 4x4 pack containing 4 Single-dose vials artesunate (73607-001-01) and 4 vials ster
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0010-2022·2021-10-13

    FDA Recalls Ultrasound Gels and Lotions for Potential Bacterial Contamination

    Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical may contain bacterial contamination. The FDA has issued a Class I recall affecting 8,702 units distributed worldwide.

    Product
    Ultra-Myossage Lotion 1-gallon bottle, REF: 4262; Myossage Lotion 1-gallon bottle, REF: 4210, located in the following DJO, LLC / DJO FRANCE kits:
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0004-2022·2021-10-13

    Betaxolol Ophthalmic Solution Recalled for Sterility Failure

    Akorn, Inc. is recalling Betaxolol Ophthalmic Solution, USP 0.5% due to confirmed sterility failure detected during stability testing. The affected lot was distributed nationwide.

    Product
    Betaxolol Ophthalmic Solution, USP, 0.5%, (Betaxolol HCl 5.6 mg/mL), 5 mL dropper bottle, Rx only, Sterile, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. Carton NDC: 17478-705-10, Bottle NDC 17478-705-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0003-2022·2021-10-13

    Firvanq Vancomycin Oral Solution Kits Recalled for Incorrect Diluent

    Azurity Pharmaceuticals is recalling 2,751 kits of Firvanq (vancomycin hydrochloride for oral solution) distributed nationwide because an incorrect diluent component was included in the kit.

    Product
    FIRVANQ — FIRVANQ (VANCOMYCIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0009-2022·2021-10-13

    Ultrasound gel distributed with medical devices recalled for bacterial contamination

    Ultrasound gel manufactured by Eco-Med Pharmaceutical and distributed with various medical device kits may contain bacterial contamination. Users should stop using affected products and follow FDA guidance.

    Product
    GEL CONDUCTOR, Description/REF: 5 LITER W/DISP/4238, 24-8.5OZ BOTTLES/4248, 5 LITER/4266, distributed by DJO, LLC / DJO FRANCE in the following kits, Part/Description: 2073/ INTELECT RPW 120V, 2073-BR/ INTELECT RPW 120V BRAZIL, 2074/ INTELECT RPW 230 V, 20
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0029-2022·2021-10-13

    Eco-Med Ultrasound Gels and Lotions Recalled for Bacterial Contamination

    Eco-Med Pharmaceutical's ultrasound gels and lotions are recalled for potential bacterial contamination. The FDA advises health care providers to stop using all affected products.

    Product
    Action De Gala, FuSion Conductive Gel - Product Usage: Intended for use in acoustic coupling of ultrasound transducer to tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0005-2022·2021-10-13

    Earle of Sandwiches Roast Beef Italiano recalled for undeclared egg

    Earle of Sandwiches X-Large Roast Beef Italiano sandwiches may contain undeclared egg. The recall affects sandwiches purchased before September 15, 2021, distributed in Minnesota, Utah, and Washington.

    Product
    Earle of Sandwiches X-Large Roast Beef Italiano, Italian Roast Beef & Swiss Cheese on Garlic Pepper French Bread. Net Wt. 10.25 oz (297g), UPC 97256 14340, Keep Refrigerated. Earle of Sandwiches, Willernie, MN 55090
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0001-2022·2021-10-13

    ALPHA MALE+ Male Enhancer Fruit Chew Strips Recalled for Unapproved Drug

    ALPHA MALE+ Male Enhancer fruit chew strips are being recalled because they contain tadalafil and were marketed without FDA approval. Consumers should stop using the product and consult a healthcare provider if they have questions.

    Product
    ALPHA MALE+ Male Enhancer, fruit chew strips, 1 strip per foil pouch, Distributed by Umbrella Labs, Made in the USA, UPC 8 60003 03770 6. Also manufactured for and distributed by: Alpha Male Plus, Tucson, AZ UPC 8 60003 74518 2 (pouch), UPC 8 60003 74512 0(carton)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V795000·2021-10-13

    Zero SR/F Motorcycles Recalled for Loose Rear Rotor Bolts

    Zero Motorcycles is recalling 2020 SR/F motorcycles because insufficiently tightened rear rotor bolts may reduce braking capability and increase crash risk.

    Product
    ZERO — ZERO SR/F
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·038-2021·2021-10-13

    Butterball Recalls Ground Turkey Products Due to Possible Blue Plastic Contamination

    Butterball is recalling approximately 14,107 pounds of ground turkey products that may contain blue plastic. The recall covers specific 2.5-lb and 3-lb trays sold nationwide.

    Product
    Butterball, LLC — Butterball, LLC Recalls Ground Turkey Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V792000·2021-10-12

    KTM and Husqvarna Recall Motorcycles for Clutch Slave Cylinder Defect

    KTM North America is recalling specific 2018-2020 KTM and Husqvarna motorcycles because a damaged gasket on the clutch slave cylinder may prevent the clutch from disengaging, increasing crash risk.

    Product
    KTM — KTM, HUSQVARNA 690 ENDURO R, 701 ENDURO LR, 690 DUKE, ENDURO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·36-2021·2021-10-08

    Nick’s Famous Bar-B-Q Recalls Smoked Pork for Listeria Risk

    Nick’s Famous Bar-B-Q is recalling approximately 3,140 pounds of ready-to-eat smoked pork barbecue products due to possible Listeria monocytogenes contamination.

    Product
    I-65 BBQ, Inc. — Nick’s Famous Bar-B-Q Recalls Ready-To-Eat Pork Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·21V785000·2021-10-08

    Forest River Recalls 2021-2022 Entrada Motorhomes Due to Brake Line Wear

    Forest River is recalling 2021-2022 Entrada motorhomes because brake lines may wear against leveling jack brackets, potentially causing brake failure and increasing crash risk.

    Product
    EAST TO WEST — EAST TO WEST ENTRADA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V782000·2021-10-07

    GM Recalls Buick Enclave and Chevrolet Traverse for Air Bag Defect

    General Motors is recalling 2008-2017 Buick Enclave and 2013-2017 Chevrolet Traverse vehicles because the driver's air bag inflator may explode during deployment.

    Product
    BUICK — BUICK, CHEVROLET ENCLAVE, TRAVERSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2582-2021·2021-10-06

    Ultrasound Gel Products Recalled for Possible Bacterial Contamination

    Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination. The FDA recommends healthcare providers stop using these products immediately.

    Product
    Norco Ultrasound Gel, Item/Description: NC70479/Norco Ultrasound Gel, 250 mL; NC70479/North Coast Ultrasound Gel, 250 mL; NC70479-5/Norco Ultrasound Gel, 5 liters; NC70479-5/North Coast Ultrasound Gel, 5 liters; NC70479-5C/Norco Ultrasound Gel, 5 liters (4); NC70479-5C/North Coas
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2592-2021·2021-10-06

    Atrium Pneumostat Chest Drain Valve Recalled Following Fatal Preterm Infant Case

    Atrium Medical Corporation is recalling 92,430 units of its Pneumostat Chest Drain Valve after a preterm infant died during treatment with the device. The company is revising product labeling and warnings.

    Product
    Atrium Pneumostat Chest Drain Valve, Part Number 16100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2583-2021·2021-10-06

    Ultrasound Gels and Lotions Recalled Due to Bacterial Contamination Risk

    Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical may contain bacterial contamination. The FDA issued a Class I recall on August 18, 2021.

    Product
    EcoLotion Transmission Lotion, used in ultrasound procedures. Item/Description: NC70481/Eco Lotion 5 liters, NC70482/Eco Lotion with Aloe 5 liters, NC70482C/Eco Lotion with Aloe 5 liters (4); Myossage Lotion, 1 Gallon, Item: NC31208
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2587-2021·2021-10-06

    GENOSYL DS vasodilator console recalled for reversed gas lines defect

    Vero Biotech recalled 3 GENOSYL DS consoles for a manufacturing defect that reverses gas inlet and outlet lines, causing delivery of toxic nitrogen dioxide instead of therapeutic nitric oxide.

    Product
    GENOSYL DS (Delivery System) console, for use as a vasodilator.
    Category
    Medical Device
    Distribution
    2 states