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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9476–9500 of 36630

  • SevereNHTSA·21V479000·2021-06-25

    SVI Trucks Recalls 2017-2021 Rescue Trucks Due to Fuel Leak Risk

    SVI Trucks is recalling 2017-2021 Rescue Trucks because a sealing washer may not seat correctly, allowing the high-pressure fuel rail to leak and increasing fire risk.

    Product
    SVI TRUCKS — SVI TRUCKS RESCUE TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V481000·2021-06-25

    Truck battery cable defect recall: Western Star and Freightliner vehicles

    Daimler Trucks North America is recalling certain Freightliner and Western Star trucks because the battery cable terminal may break, causing engine stall and crash risk. Dealers will repair or replace the cables at no cost.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR CASCADIA, WH126, WJ121, 49X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V478000·2021-06-25

    Mercedes-Benz Recalls AMG GT Vehicles for Driveshaft Separation Risk

    Mercedes-Benz is recalling 2016-2018 AMG GT vehicles because an insufficient bond between the carbon-fiber driveshaft and flange could cause separation, leading to loss of drive power and increased crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V473000·2021-06-24

    GM Recalls Cadillac SRX and Saab 9-4X for Rear Suspension Defect

    General Motors is recalling 2010-2016 Cadillac SRX and 2011-2012 Saab 9-4X vehicles because a rear suspension part may be loose, increasing crash risk.

    Product
    CADILLAC — CADILLAC, SAAB SRX, 9-4X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V470000·2021-06-23

    Audi Recalls A4, S4, and TT Models for Airbag Inflator Defect

    Volkswagen Group of America is recalling 2000-2002 Audi A4, S4, and 2000-2001 TT vehicles because driver airbag inflators may absorb moisture, potentially causing improper deployment in a crash.

    Product
    AUDI — AUDI A4, S4, TT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1860-2021·2021-06-23

    Medtronic Angiographic Guidewire Components Shipped Without Required Sterilization

    Medtronic Vascular recalled 54,997 angiographic guidewire components that were shipped directly to customers without the required downstream processing and sterilization. The components should have been sent to a third-party processor first.

    Product
    Angiographic Guidewire Component: Model Number: 107042, 107044, 107447, 110003, 110004, The angiographic guidewire components associated with this recall are manufactured with a requirement that further downstream processing (sterilization) is required. Indications for use fo
    Category
    Medical Device
    Distribution
    11 states
  • SevereFDA (Drugs)·D-0628-2021·2021-06-23

    Imperia Elita Vitaccino Coffee Recalled for Unapproved Drug Ingredients

    Imperia Elita Vitaccino Coffee sachets are being recalled because they were marketed without FDA approval and contain pharmaceutical ingredients Sibutramine and Fluoxetine. All lots distributed nationwide are affected.

    Product
    Imperia Elita Vitaccino Coffee, 10 g sachets, 15 sachets per box, Global Beauty Technologies, Manufactured for: Imperia-Elita Ltd. & Co, KG D- 35435 Wettenberg
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0667-2021·2021-06-23

    Olde Thompson and Sun Harvest Organic Coriander Recalled for Salmonella

    Olde Thompson and Sun Harvest are recalling 1.5oz. jars of organic ground coriander due to potential Salmonella contamination. Affected lots are 23631 and 23632 with best-before dates of 05/2023.

    Product
    Olde Thompson Organic Ground Coriander 1.5oz. in glass jar with flip-top lid. Sun Harvest Organic Coriander 1.5oz in glass jar with flip-top lid. UPC code: 400000290942 Olde Thompson item numbers: 1901-43, 1901-43CA, 1901-43SU
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0675-2021·2021-06-23

    BulkFoods.com Dehydrated Celery Recalled for Salmonella Risk

    Natural Foods Inc is recalling BulkFoods.com brand dehydrated chopped celery in 1lb and 5lb bags due to potential Salmonella contamination. The affected product was distributed to multiple states.

    Product
    BulkFoods.com brand dehydrated chopped celery in 1lb and 5lb plastic bags
    Category
    Food
    Distribution
    23 states
  • SevereNHTSA·21V468000·2021-06-23

    Alexander Dennis Recalls 2017-2020 Enviro 500 Buses for Fuel Leak Risk

    Alexander Dennis is recalling 2017-2020 Enviro 500 buses because a sealing washer defect may cause high-pressure fuel leaks, increasing fire risk.

    Product
    ALEXANDER DENNIS — ALEXANDER DENNIS ENVIRO 500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0668-2021·2021-06-23

    Organic Gemini TigerNut Flour Recalled for Salmonella Contamination

    HMO Beverage Corp. dba Organic Gemini LLC is recalling Organic Gemini TigerNut Flour (27.5 lb bags) because the product may be contaminated with Salmonella. Consumers should not consume the affected product.

    Product
    ORGANIC GEMINI TigerNut Flour, Ingredients: 100% Organic Tiger Nuts; 27.5lbs; Lot: TM2-24200RFFF1; EXP: 10/2021
    Category
    Food
    Distribution
    4 states
  • SevereNHTSA·21V464000·2021-06-18

    Altec Recalls 2020-2021 Aerial Devices Due to Weak Bolts

    Altec is recalling 2020-2021 AT200A, AT235, and AT235P aerial devices because insufficient strength bolts may fail, causing the pedestal to separate and increasing the risk of injury or death.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V463000·2021-06-18

    Trailstar Recalls 2017-2019 Dump Trailers Due to Steering Arm Defect

    Trailstar is recalling 2017-2019 Dump Trailers because the steering arm may detach, potentially causing loss of steering control or road hazards.

    Product
    TRAILSTAR — TRAILSTAR DUMP TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V461000·2021-06-17

    2020-2021 Nissan Sentra Vehicles Recalled for Bent Tie Rod Defects

    Nissan is recalling 2020-2021 Sentra vehicles because the left or right tie rod may be bent. A bent tie rod can break, causing loss of steering control and increasing crash risk.

    Product
    NISSAN — NISSAN SENTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1786-2021·2021-06-16

    Medical Convenience Kits Recalled Due to Mold Contamination Risk

    Avid Medical is recalling 160 fistula care kits due to potential contamination from Aspergillus penicillioides fungal growth in a component applicator. The contamination could breach the kit's package integrity and affect other sterile components.

    Product
    FISTULA (ON/OFF) ALL IN ONE BAG. Medical convenience kit, Avid Medical Part Number: VAMK024-03
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1787-2021·2021-06-16

    Dialysis access kits recalled for potential fungal contamination risk

    Avid Medical is recalling medical dialysis access kits due to potential fungal growth in an applicator component that may compromise the package seal and contaminate other components. Approximately 560 kits distributed nationwide are affected.

    Product
    DIALYSIS ACCESS Medical convenience kit, Avid Medical Part Number: VMED004-03.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1832-2021·2021-06-16

    DeRoyal Pacemaker Tray Mislabeled With Wrong Anesthetic Concentration

    DeRoyal is recalling surgical procedure packs due to mislabeling. The product contains 0.5% Bupivacaine but is labeled as 1% Lidocaine, creating a medication identification error.

    Product
    DeRoyal Pacemaker Tray Pgybk, REF 89-6360.06
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0748-2021·2021-06-16

    Enoki Mushroom Recalled for Listeria monocytogenes Contamination

    Rainfield Marketing Group is recalling 150g packages of Enoki Mushroom (UPC 085412004020) because samples tested positive for Listeria monocytogenes. The product was distributed to California, Texas, and Maryland.

    Product
    Enoki Mushroom, 150g clear plastic bag with orange bottom; UPC 085412004020 Product of Korea Do no consume Raw Distributed by Rainfield Marketing Group
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0674-2021·2021-06-16

    BC Foods Celery Stalk and Leaf Dice Recalled for Salmonella

    BC Foods is recalling Celery Stalk and Leaf Dice due to an ingredient testing positive for Salmonella. The product was distributed to food manufacturers and distributors across eight states.

    Product
    BC Foods Celery Stalk and Leaf Dice 3/8, AD Sulfites, 11 lb. Poly lined bulk fiber carton. Item code: VCE1-D38-AXG-AB-AR
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Devices)·Z-1798-2021·2021-06-16

    Jelco Insulin Syringe Graduation Markings Recalled for Skew Defect

    Smiths Medical recalls 1,432,200 Jelco insulin syringes with skewed graduation markings that could lead to incorrect dosing. Specific lot numbers are affected.

    Product
    JELCO HYPODERMIC NEEDLE-PRO FIXED NEEDLE INSULIN SYRINGE: a) 1.0mL 28G X 1/2" (0.33mm x 13mm), REF 4428-1 b) 1.0mL 29G X 1/2" (0.33mm x 13mm), REF 4429-1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1785-2021·2021-06-16

    Avid Medical Fistula On-Off Kit Recalled for Potential Fungal Contamination

    Avid Medical is recalling 720 Fistula On-Off Kits due to potential fungal contamination that may compromise package integrity. The BD ChloraPrep applicator component may develop Aspergillus penicillioides, which could contaminate other kit components.

    Product
    FISTULA ON-OFF KIT. Medical convenience kit, Avid Medical Part Number: MMTN020.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1538-2021·2021-06-16

    INNOVA SARS-CoV-2 Antigen Rapid Tests Recalled for Unauthorized Non-Clinical Distribution

    INNOVA Medical Group is recalling SARS-CoV-2 antigen rapid test kits distributed to customers not enrolled in an authorized clinical investigation.

    Product
    For In Vitro Diagnostic Use Only *** 25T 888 SARS-CoV-2 Antigen *** SARS-CoV-2 Antigen Rapid Qualitative Test *** REF BT1309
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1784-2021·2021-06-16

    Adult Chest Tube Tray Recalled Due to Package Integrity Risk

    Avid Medical is recalling 130 Adult Chest Tube Trays due to potential contamination from mold growth in a component. The BD ChloraPrep applicator may grow Aspergillus penicillioides, which could breach package integrity and contaminate other kit components.

    Product
    ADULT CHEST TUBE TRAY. Medical convenience kit, Avid Medical Part Number: LAKC001-04
    Category
    Medical Device
    Distribution
    Distributed nationwide