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.

6626–6650 of 29119

  • SevereFDA (Food)·F-1123-2022·2022-06-08

    JIF Peanut Butter Recalled for Potential Salmonella Contamination

    JIF 454 gram crunchy peanut butter from specific lot codes is being recalled due to potential Salmonella contamination. Affected products were distributed nationwide.

    Product
    JIF 454 GRAM CRUNCHY PEANUT BUTTER MEXICO
    Category
    Food
    Distribution
    49 states
  • SevereFDA (Food)·F-1122-2022·2022-06-08

    JIF Creamy Peanut Butter Recalled for Potential Salmonella Contamination

    The JM Smucker Company is recalling 20,021 cases of JIF 340-gram Creamy Peanut Butter due to potential Salmonella contamination. Affected products distributed nationwide should not be consumed; consumers should discard or return them.

    Product
    JIF 340 GRAM CREAMY PEANUT BUTTER MEXICO
    Category
    Food
    Distribution
    49 states
  • SevereFDA (Food)·F-1121-2022·2022-06-08

    JIF Creamy Peanut Butter To Go Recalled Due to Salmonella Risk

    The JM Smucker Company is recalling JIF 1.5 oz and 31.25 gram Creamy Peanut Butter To Go packages due to potential Salmonella contamination. These products were distributed to all 50 states.

    Product
    JIF 1.5 oz and 31.25 gram CREAMY PEANUT BUTTER TO GO packaged in 3, 8, 36, and 96 count cases
    Category
    Food
    Distribution
    49 states
  • SevereFDA (Food)·F-1140-2022·2022-06-08

    Milk Peanut Butter Cups Recalled for Potential Salmonella Contamination

    Walnut Creek Chocolate Co Inc is recalling Milk Peanut Butter Cups due to potential Salmonella contamination. The FDA Class I recall affects 3,276 units distributed across 30 US states.

    Product
    Milk Peanut Butter Cups
    Category
    Food
    Distribution
    29 states
  • SevereNHTSA·22V398000·2022-06-07

    C.E. Smith and Malone Auto Racks Recall Boat Trailers Due to Axle Weld Failure

    C.E. Smith is recalling 2021-2022 boat trailers because a weld may fail, causing the wheel to separate and increasing crash risk.

    Product
    MALONE AUTO RACKS — MALONE AUTO RACKS, C.E. SMITH COMPANY MICROSPORT MPG460, MULTI-SPORT 48810, ECOLIGHT MPG585, MULTI-SPORT 48815
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V394000·2022-06-03

    2023 Freightliner M2 Trucks Steering Shaft Defect Recall

    Daimler Trucks North America is recalling 2023 Freightliner Business Class M2 trucks due to a u-joint pinch bolt that may detach from the steering shaft, causing loss of steering control and increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER BUSINESS CLASS M2, 114SD, 108SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22T009000·2022-06-02

    Goodyear Recalls G159 Tires Due to Tread Separation Risk

    Goodyear is recalling specific G159 tires because the tread may separate, increasing the risk of a crash. Owners should contact dealers for free replacement.

    Product
    TIRES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·22147·2022-06-02

    Backcountry Access Tracker4 Avalanche Transceivers Recalled for Toggle Switch Failure

    Backcountry Access Tracker4 Avalanche Transceivers are being recalled because the toggle switch can separate from the unit and prevent it from switching to search mode, which could prevent rescuers from locating a buried skier.

    Product
    Backcountry Access Tracker4 Avalanche Transceivers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1076-2022·2022-06-01

    Champon Soup Base recalled for undeclared milk and tuna allergens

    Joonsung Trading Inc recalls Champon Soup Base due to undeclared milk and tuna allergens. Affected 32 oz containers were distributed in Oregon and Washington; products dated before April 14, 2022 are recalled.

    Product
    Champon Soup Base packaged in 32 oz plastic jug. The label is read in part "Hot Pepper, Soy bean oil, Chicken soup base, Hondash, Garlic"
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-1077-2022·2022-06-01

    Chirashi Sauce recalled for undeclared soy and wheat allergens

    Joonsung Trading Inc is recalling Chirashi Sauce in 1/2 gallon jugs because the label fails to declare soy and wheat allergens present in the product.

    Product
    Chirashi Sauce packaged in 1/2 gallon plastic jug. Label read in parts: "Korean hot bean paste, Reg. Vinegar, Sugar, Sake, Garlic powder, 7up".
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-1098-2022·2022-06-01

    Sara Plus Active Floor Lift Recalled for Smoke and Ignition Risk

    The FDA is recalling approximately 4,449 Sara Plus Active Floor Lift devices due to a fire hazard. The devices may emit smoke or ignite, posing a risk to users and staff.

    Product
    Sara Plus Active Floor Lift
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1081-2022·2022-06-01

    French Beans Recalled for Potential Listeria Contamination

    Hippie Organics French Beans, 1Lb packages (Lot IM313626) are recalled due to potential Listeria monocytogenes contamination. Alpine Fresh, Inc. notified the FDA after a positive test result.

    Product
    Hippie Organics- French Beans, 1Lb, UPC 1588701137
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1087-2022·2022-06-01

    Bantam Bagels Everything Bagel Recalled for Undeclared Egg Allergen

    Damascus Bakery LLC is recalling Bantam Bagels Everybody's Favorite Everything Bagels due to undeclared egg allergen. The affected product was distributed to a consignee in Georgia.

    Product
    Bantam Bagels Everybody's Favorite Everything Bagel Stuffed with Veggie Cream Cheese, 6/1.3 oz pieces per carton (Net Wt. 7.8 oz.), Paper Carton, 6 cartons / case. Keep Frozen
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1080-2022·2022-06-01

    Sunomono Vinegar Recalled for Undeclared Soy and Wheat

    Sunomono Vinegar in 5-gallon jugs is recalled due to undeclared soy and wheat allergens. Consumers with allergies should avoid this product.

    Product
    Sunomono Vinegar packaged in 5 gallon plastic jug. Label read in parts: "Ingredient: Reg. vinegar, Sugar, Salt, Mirin".
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-1124-2022·2022-06-01

    Benzonatate 100mg Capsules Label Mix-up — Wrong Medication in Bottles

    Benzonatate 100mg capsule bottles are mislabeled. Some contain Benzphetamine tablets instead, and vice versa. This medication mix-up affects 10 bottles distributed to one physician in Alpharetta, Georgia.

    Product
    Benzonatate capsules, 100mg, repackaged in 30-count bottles, Distributed by Calvin Scott & Co., Inc, Albuq., NM. 87123, NDC 67877-0573-05
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Food)·F-1079-2022·2022-06-01

    Spicy Chicken Sauce recalled due to undeclared wheat allergen

    Joonsung Trading Inc is recalling Spicy Chicken Sauce in 1/2 gallon plastic jugs because the product contains wheat but the label does not declare it. This poses a serious risk to consumers with wheat allergies.

    Product
    Spicy Chicken Sauce packaged in 1/2 gallon plastic jug. Label read in parts "Ingredient: Soy sauce (Gluten free), Sugar, Korean hot bean paste, Garlic powder, Ginger powder, Mirin, Korean hot pepper, Sambal hot sauce"
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-1078-2022·2022-06-01

    Mio Salad Dressing Recalled for Undeclared Egg Allergen

    Joonsung Trading Inc recalls Mio Salad Dressing due to undeclared egg allergen. The label lists Mayo but fails to declare Egg, creating serious risk for egg-allergic consumers.

    Product
    Mio Salad Dressing packaged in 1 gallon plastic jug. Label read in parts: "Ingredient: Onion, Carrot, Ginger water, Soybean oil, Reg. Vinegar, Mayo, Sushi Ginger".
    Category
    Food
    Distribution
    2 states
  • SevereNHTSA·22V388000·2022-05-30

    Escape Trailer Recalls 2018-2021 Models Due to Gas Leak Risk

    Escape Trailer is recalling 2018-2021 travel trailers because aluminum burner tubes can fracture, causing a gas leak that may lead to fire.

    Product
    ESCAPE — ESCAPE, ESCAPE RV ESCAPE 5.0, ESCAPE 19, ESCAPE 17, ESCAPE 21
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22E047000·2022-05-28

    R.H. Sheppard Recalls Steering Gears Due to Fracture Risk

    R.H. Sheppard is recalling specific steering gears that may have been assembled incorrectly, posing a risk of fracture and loss of steering control.

    Product
    STEERING recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0867-2022·2022-05-25

    Milk of Magnesia USP Recalled for Microbial Contamination

    Plastikon Healthcare LLC is recalling Milk of Magnesia USP (2400 mg/30 mL) distributed in Indiana due to microbial contamination in this non-sterile product. The FDA classified this as a Class I recall.

    Product
    MILK OF MAGNESIA USP, (Magnesium Hydroxide), 2400 mg/30 mL, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Distributed by Major Pharmaceuticals, Livonia, MI 48152, NDC 0904-6846-73.
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1095-2022·2022-05-25

    Dragonfly OpStar Imaging Catheter Recall Due to Proximal Marker Separation Risk

    Abbott Vascular recalls 14,544 Dragonfly OpStar Imaging Catheters due to potential separation of the proximal marker. The affected devices were distributed throughout the US and internationally.

    Product
    Dragonfly OpStar Imaging Catheter, REF 1014651/1014652, 0.068 in, 0.014 in, 135 cm, STERILE EO
    Category
    Medical Device
    Distribution
    44 states