The Recall Desk

Severity 4 of 5

Severe recalls

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

What “severe” means here

Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

7426–7450 of 29119

  • SevereNHTSA·21E099000·2021-12-01

    Cummins Recalls X12 Diesel Engines Due to Fuel Tube Cracking Risk

    Cummins is recalling X12 Diesel Engines because fuel tubes may crack, causing high-pressure leaks that increase fire risk.

    Product
    FUEL SYSTEM, DIESEL:FUEL INJECTION SYSTEM:FUEL RAIL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·22023·2021-12-01

    DEWALT Jobsite Pro Wireless Earphones Recalled for Burn and Fire Hazards

    E-filliate is recalling about 301,800 DEWALT Jobsite Pro Wireless Earphones because they can overheat during charging or use, posing burn and fire hazards. The company has received 61 reports of overheating, including five fires and four minor burn injuries.

    Product
    DEWALT ® Jobsite Pro Wireless Earphones
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V934000·2021-12-01

    Mercedes-Benz Recalls 2021 Sprinter Vans for Rear Step Bolt Issue

    Daimler Vans USA is recalling 2021 Mercedes-Benz Sprinter vans because improperly tightened rear step bolts could allow the step to separate, creating a road hazard.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 4500, SPRINTER 2500, SPRINTER 1500, SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V933000·2021-12-01

    2021 Mercedes-Benz Sprinter Vehicles Recalled for Brake Hose Damage Risk

    Daimler Vans USA is recalling 2021 Mercedes-Benz and Freightliner Sprinter vans because the front fender liner may damage the brake hose, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 3500, SPRINTER 4500, SPRINTER 1500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21T018000·2021-11-30

    Sailun Recalls Specific Tires Due to Belt Separation Risk

    Sailun is recalling specific ST235/80R16 and ST235/85R16 tires due to a manufacturing issue that may cause belt separation. This defect could lead to loss of vehicle control and increase crash risk.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E098000·2021-11-30

    Meritor Recalls 180 Series Drive Pinions Due to Fracture Risk

    Meritor is recalling 180 Series Drive Pinions because they may fracture and engage the parking brake without warning, increasing crash risk.

    Product
    POWER TRAIN:AXLE ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E097000·2021-11-30

    Tenneco Recalls MOOG and NAPA Tie Rods Due to Heat Treatment Defect

    Tenneco Automotive is recalling specific MOOG and NAPA tie rods that may not have been heat-treated properly. This defect can cause tie rod failure and loss of steering control.

    Product
    STEERING:LINKAGES:TIE ROD ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V932000·2021-11-29

    Honda Recalls 2016-2020 Models for Hood Latch Striker Defect

    Honda is recalling specific Passport, Pilot, and Ridgeline vehicles because a damaged hood latch striker may cause the hood to open while driving, obstructing the driver's view.

    Product
    HONDA — HONDA RIDGELINE, PASSPORT, PILOT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V923000·2021-11-24

    2022 Ford Super Duty F-250 and F-350 Driver-Side Air Bag Cover Defect Recall

    Ford is recalling 2022 Super Duty F-250 and F-350 vehicles due to an insufficient driver-side air bag cover that may break apart during a crash, projecting fragments toward occupants and increasing injury risk.

    Product
    FORD — FORD F-350 SD, F-250 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0186-2022·2021-11-24

    Hardies Onion Yellow Jumbo Recalled for Salmonella Contamination Risk

    Hardies Fruit & Vegetable Co., LP is recalling Onion Yellow Jumbo packed in 5-pound boxes due to potential Salmonella contamination. Consumers should not consume the affected product.

    Product
    Onion Yellow Jumbo packed in a 5 pound cardboard box Product Code 2377
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0249-2022·2021-11-24

    Lotrimin Daily Prevention Deo Tolnaftate Spray Recalled for Benzene Contamination

    Bayer Healthcare Pharmaceuticals is recalling Lotrimin Daily Prevention Deo (Tolnaftate 1%) spray powder due to the presence of benzene contamination. The recall affects 579,456 cans distributed nationwide.

    Product
    LOTRIMIN DAILY PREVENTION DEO — LOTRIMIN DAILY PREVENTION DEO (TOLNAFTATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0242-2022·2021-11-24

    Tinactin Tolnaftate Deodorant Powder Spray Recalled for Benzene Contamination

    Bayer Healthcare is recalling Tinactin (Tolnaftate 1%) Deodorant Powder Spray due to potential benzene contamination. The product was manufactured at a facility where other lots tested positive for benzene.

    Product
    TINACTIN — TINACTIN (TOLNAFTATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0251-2022·2021-11-24

    Tinactin Tolnaftate Liquid Spray Recalled for Benzene Contamination

    Bayer Healthcare Pharmaceuticals is recalling Tinactin (Tolnaftate 1%) liquid spray due to the presence of benzene chemical contamination. The product was distributed nationwide through retail channels.

    Product
    TINACTIN — TINACTIN (TOLNAFTATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0250-2022·2021-11-24

    Tinactin Tolnaftate Deodorant Powder Spray Recalled for Benzene Contamination

    Bayer Healthcare Pharmaceuticals is recalling Tinactin (Tolnaftate 1%) Deodorant Powder Spray due to the presence of benzene chemical contamination. The recall affects 738,432 cans distributed nationwide and internationally.

    Product
    TINACTIN — TINACTIN (TOLNAFTATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0205-2022·2021-11-24

    EveryPlate Meal Kits Recalled for Salmonella Contamination

    HelloFresh is recalling specific EveryPlate meal kits containing onions from ProSource that are associated with a Salmonella Oranienburg outbreak. Affected product codes from production week 08/25/2021 are being recalled nationwide.

    Product
    EveryPlate Meal Kit Product Codes 87-88-89-90-91-94-101 from Production Week 35 (production week start date: 08/25/2021)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0189-2022·2021-11-24

    HelloFresh Meal Kit Recalled for Salmonella-Contaminated Onions

    HelloFresh is recalling meal kits containing onions from ProSource that may be contaminated with Salmonella Oranienburg. The affected product is from Production Week 28 (starting July 7, 2021) and was distributed nationwide.

    Product
    HelloFresh Meal Kit Product Code 2-7-17-19-21-25-AB from Production Week 28 (production week start date: 07/07/2021)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0180-2022·2021-11-24

    Red Jumbo Onions Recalled for Potential Salmonella Contamination

    JF Palmer & Sons Produce is recalling 1,040 bags of red jumbo onions due to potential Salmonella contamination. The affected onions were distributed to MN, TX, CA, and MD.

    Product
    Onions Red Jumbo, packaged in 25 pound bulk bags
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0184-2022·2021-11-24

    Green Giant Fresh Whole White Onions Recalled for Salmonella

    Green Giant Fresh brand whole white onions in 2 lb. bags are being recalled due to potential Salmonella Oranienburg contamination. The affected onions were distributed in Minnesota and North Dakota.

    Product
    Green Giant Fresh brand, Whole WHITE Onions packaged in 2 lb. flexible mesh bags, UPC 60580600218-2.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0200-2022·2021-11-24

    EveryPlate Meal Kits Recalled for Salmonella Contamination

    HelloFresh US is recalling specific EveryPlate meal kits containing onions contaminated with Salmonella Oranienburg. The affected products are from production week starting July 21, 2021, with product codes 84, 88, 89, 90, 91, 92, 94, 98, 99, and 100.

    Product
    EveryPlate Meal Kit Product Codes 84-88-89-90-91-92-94-98-99-100 from Production Week 30 (production week start date: 07/21/2021)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0171-2022·2021-11-24

    Whole White Onions Recalled for Potential Salmonella Contamination

    Keeler Family Farms is recalling whole white onions imported from Chihuahua, Mexico due to potential contamination with Salmonella Oranienburg. The affected onions were shipped between July 1 and August 25, 2021.

    Product
    Whole raw onions - WHITE - imported from Chihuahua, Mexico and shipped from July 1, 2021 through August 25, 2021. Products are packaged in 25 lb. and 50 lb. mesh bags. One pallet contains 42 bags. Store in cool dry place off the ground. Labeling will state product of Mexico on bi
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0210-2022·2021-11-24

    Dole Garden Salad Recalled for Listeria monocytogenes

    Dole Fresh Vegetables Inc is recalling Salad Classics Garden Salad (12 oz) due to Listeria monocytogenes contamination found by the Georgia Department of Agriculture. The product was distributed across multiple states.

    Product
    Salad Classics Garden Salad; iceberg lettuce, shredded carrots, red cabbage; Net Wt. 12 oz. (340g) UPC: 6-88267-18443-7 Packaged by Dole Distributed by F-------Old USA, Landover, MD
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Devices)·Z-0234-2022·2021-11-24

    Arrow-Trerotola Percutaneous Thrombolytic Device: Inner Lumen Detachment Risk

    Arrow International is recalling 1918 units of the Arrow-Trerotola Percutaneous Thrombolytic Device due to inner lumen detachment that can cause embolization, requiring emergency retrieval and delaying treatment.

    Product
    Arrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR Product Code: PT-65709-WC The Arrow-Trerotola" Percutaneous Thrombolytic Device (PTDTM) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits mechanical declotting of native arterio-venous
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0208-2022·2021-11-24

    Marketside Garden Salad recalled due to Listeria contamination

    Dole Fresh Vegetables Inc is recalling Marketside Classic Salad (Garden Salad) because samples tested positive for Listeria monocytogenes. The product was distributed to multiple states.

    Product
    Marketside Classic Salad; Garden Salad; iceberg lettuce, shredded carrots, red cabbage; Net Wt. 24 oz. (1 lb. 8 oz.) 680 g UPC: 6-81131-32895-1 Distributed by Walmart, Bentonville, AR
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Devices)·Z-0224-2022·2021-11-24

    FDA Recalls Scrip Ultrasound Gel for Potential Bacterial Contamination

    Scrip Inc is recalling Scrip Ultrasound Gel Clear (5L) nationwide due to potential bacterial contamination. Affected units may cause harm if contaminated product contacts patients during ultrasound procedures.

    Product
    Scrip Ultrasound Gel Clear, 5L Intended for use in acoustic coupling of ultrasound transducer to tissue
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0246-2022·2021-11-24

    Lotrimin AF Deodorant Powder Spray Recalled for Benzene Contamination

    Bayer Healthcare is recalling Lotrimin AF Deodorant Powder Spray (Miconazole nitrate 2%) nationwide due to the presence of benzene contamination. The recall affects approximately 2.8 million cans distributed across the US, Puerto Rico, Canada, and Mexico.

    Product
    LOTRIMIN AF (Miconazole nitrate 2%) Deodorant Powder Spray, NET WT 133g (4.6 OZ) can, Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Spain, NDC 11523-1272-2 UPC 3 11017 41023 3
    Category
    Drug
    Distribution
    Distributed nationwide