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.

6301–6325 of 29111

  • SevereNHTSA·22V564000·2022-08-02

    Delco Trailers Recalls 2021-2022 Models Due to Axle Weld Defect

    Delco Trailers is recalling 2021-2022 C, D, and F-Series trailers because a defective axle weld may crack or separate, increasing crash risk.

    Product
    DELCO TRAILERS — DELCO TRAILERS C-SERIES, F-SERIES, D-SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V565000·2022-08-02

    Travel Trailers Recalled for Improperly Tightened Axle Bolts

    Xtreme Outdoors is recalling 2021-2022 Little Guy Max and Mini Max travel trailers with improperly tightened axle bolts that could cause axle detachment and increase crash risk.

    Product
    XTREME OUTDOORS — XTREME OUTDOORS LITTLE GUY MINI MAX, LITTLE GUY MAX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V558000·2022-08-01

    Forest River Rockwood and Flagstaff tent campers recalled for defective brake axle

    Forest River is recalling certain 2022 Flagstaff and 2022-2023 Rockwood tent campers due to improperly installed axles that can reduce brake function. Owners should contact their dealer for free inspection and repair.

    Product
    FOREST RIVER — FOREST RIVER FLAGSTAFF, ROCKWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·025-2022·2022-07-30

    Conagra Recalls P.F. Chang's Beef and Broccoli for Undeclared Egg

    Conagra Brands is recalling P.F. Chang's Home Menu Beef & Broccoli because the product contains egg, an undeclared allergen. No illnesses have been reported.

    Product
    Conagra Brands (Conagra Foods Packaged Foods, LLC) — Conagra Brands, Inc., Recalls Frozen Beef Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V553000·2022-07-29

    2023 Thomas Built School Buses Recalled for Engine Control Module Defect

    Daimler Trucks North America is recalling 2023 Thomas Built Saf-T-Liner HDX and C2 school buses because the engine control module may short-circuit, causing unexpected engine shutdown.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX, SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·023-2022·2022-07-28

    Danny's Sub and Pizza Recalls Frozen Meat Pizzas Lacking Federal Inspection

    USDA FSIS is recalling approximately 19,275 pounds of frozen meat pizzas from Danny's Sub and Pizza because they were produced without federal inspection.

    Product
    Danny’s Sub and Pizza Recalls Meat Pizza Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    2 states
  • SevereNHTSA·22V549000·2022-07-28

    Nissan Recalls 2017-2019 Rogue Hybrid for Brake Booster Overheating

    Nissan is recalling 2017-2019 Rogue Hybrid vehicles because the hydraulic brake booster may overheat, causing a loss of power brake assist and increasing crash risk.

    Product
    NISSAN — NISSAN ROGUE HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V551000·2022-07-28

    Eldorado Axess Recalled for Potential Steering Gear Fracture

    Eldorado is recalling 2021-2022 Axess vehicles because incorrectly assembled steering gears may fracture, causing loss of steering control and increasing crash risk.

    Product
    ELDORADO — ELDORADO AXESS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·22193·2022-07-28

    Evaporator Coil Drain Pans Recall for Fire Hazard Risk

    Daikin Comfort Technologies is recalling about 298,300 evaporator coil drain pans that can overheat, melt, and deform, creating a fire hazard. The company has received 26 fire reports, with no injuries reported.

    Product
    Evaporator coil drain pans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1501-2022·2022-07-27

    Blazos Pie Shoppe Products Recalled for Possible Salmonella Contamination

    Blazos Pie Shoppe is recalling peanut butter cream and chocolate peanut butter cream pie and cup products that may be contaminated with Salmonella.

    Product
    10 oz Blazos Pie Shoppe Peanut Butter Cream Cup (UPC 9438600085)
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1502-2022·2022-07-27

    Panera Bread Southwest Corn Chowder Recalled for Undeclared Wheat

    Blount Fine Foods is recalling Panera Bread at Home Southwest Corn Chowder due to undeclared wheat. The product poses a health risk to consumers with wheat allergies or celiac disease.

    Product
    Panera Bread at Home Southwest Corn Chowder, 16 oz. (453 g)
    Category
    Food
    Distribution
    12 states
  • SevereFDA (Devices)·Z-1389-2022·2022-07-27

    GE Healthcare Anesthesia Systems Recalled for Potential Transducer Connection Reversal

    GE Healthcare anesthesia systems may have reversed oxygen and air transducer connections, potentially affecting proper gas delivery. 5,372 devices worldwide are affected.

    Product
    GE Healthcare Aisys CS2 Anesthesia System, Part number 1011-9050-000; and Avance CS2 and Avance CS2 Pro Anesthesia System, Part number 1009-9050-000.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1297-2022·2022-07-27

    Artri King Herbal Supplement Tablets Recalled Nationwide for Undeclared Medication

    Amazon is recalling Artri King herbal supplement tablets nationwide due to FDA laboratory findings of undeclared diclofenac, a pharmaceutical medication not listed on the label. The product was marketed without FDA approval.

    Product
    Artri King Reforzado con Ortiga y Omega 3 tablets, 500 mg, 100-count bottle, Hecho en Mexico por: PLANTAS MEDICINALES DE MEXICO , Melchor Ocampo No. 55 Local D, Delegacion Xochimilco. C.P. 16800, Mexico, D.F., ASIN B084KSV12L, UPC 7 501031 111190
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1296-2022·2022-07-27

    Ortiga mas Ajo Rey supplement recalled for undeclared diclofenac

    FDA recalls Ortiga mas Ajo Rey dietary supplement sold nationwide due to undeclared diclofenac. Product marketed as supplement contains pharmaceutical ingredient not listed on label.

    Product
    Ortiga mas Ajo Rey Reforzado con Omega 3, 6 y 9, is packaged in a carton containing 30 tablets (500 mg c/u) in a bottle and 60 capsules (400 mg c/u) in a bottle, Hecho en Mexico por: Omega Nutrition , Jorge Washington No. 108 Col. Las Americas, Hidalgo del Parral, Chihuahua. C.P
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1336-2022·2022-07-27

    Dietary supplement found to contain undeclared pharmaceutical drug tadalafil

    Launch Sequence Capsules dietary supplement recalled for containing undeclared tadalafil, an FDA-approved pharmaceutical ingredient. The product was marketed without required drug approval.

    Product
    Launch Sequence Capsules, Dietary Supplement, 60- count bottles, ASIN B07TLPWXDS, UPC Code 641378938375.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1337-2022·2022-07-27

    FDA Recalls Launch Sequence Euphoria Capsules for Undeclared Tadalafil

    Launch Sequence Euphoria Capsules have been recalled because the product contains undeclared tadalafil, an unapproved active ingredient. The capsules were distributed nationwide in the USA and Canada.

    Product
    Launch Sequence Euphoria Capsules, 10- count tins, ASIN B08ZJX4V9J, UPC Code 661020846864.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1295-2022·2022-07-27

    Artri Ajo King Tablets Recalled Due to Undeclared Diclofenac

    The FDA is recalling Artri Ajo King tablets nationwide after finding they contain undeclared diclofenac, a prescription anti-inflammatory drug. Affected bottles (lot LTARTKNGOMG30220, expiring December 2025) were sold on Amazon.

    Product
    Artri Ajo King Reforzado con Ortiga y Omega 3 tablets, 500 mg, 100-count bottle, Hecho en Mexico por: PLANTAS MEDICINALES DE MEXICO , Melchor Ocampo No. 55 Local D, Delegacion Xochimilco. C.P. 16800, Mexico, D.F., ASIN B092P4615M, UPC 7 501031 111190
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V543000·2022-07-27

    Volkswagen Recalls 2016 Audi and Golf Models for Air Bag Defect

    Volkswagen is recalling 1,216 2016 Audi and Volkswagen vehicles because the front passenger air bag may explode or deploy improperly, posing a risk of serious injury or death.

    Product
    AUDI — AUDI, VOLKSWAGEN S3, A3 SPORTBACK E-TRON, GTI, GOLF R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1500-2022·2022-07-27

    Blazos Pie Shoppe peanut butter cream pies recalled for possible Salmonella contamination

    Blazos Pie Shoppe is recalling 9-inch peanut butter cream pies possibly contaminated with Salmonella. The affected products with code dates 6/23 and 6/27 were distributed in Michigan.

    Product
    9-inch pie Blazos Pie Shoppe Chocolate Peanut Butter Cream Pie (UPC 9438600049) 9-inch pie Blazos Pie Shoppe Peanut Butter Cream Pie (UPC 9438600025)
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1338-2022·2022-07-27

    Launch Sequence Aphrodisia Capsules recalled for undeclared tadalafil

    Launch Sequence Aphrodisia Capsules contain undeclared tadalafil, making them an unapproved drug. The recall involves 500 4-count tins distributed nationwide in the USA and Canada.

    Product
    Launch Sequence Aphrodisia Capsules, 4-count tins, ASIN B07QB3S2LV, UPC Code 661020846957.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V537000·2022-07-26

    Capacity Recalls 2021-2022 TJ Trucks for Steering Gear Fracture Risk

    Capacity of Texas is recalling 2021-2022 TJ 5000, 6500, and 9000 trucks because incorrectly assembled steering gears may fracture, causing loss of steering control.

    Product
    CAPACITY — CAPACITY TJ 9000, TJ 6500, TJ 5000
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V539000·2022-07-26

    Spartan Fire Recalls 2020-2021 Metrostar and Gladiator Trucks for Fire Risk

    Spartan Fire is recalling 2020-2021 Metrostar and Gladiator fire trucks because a loose electrical connection may cause the load center to overheat and increase the risk of a fire.

    Product
    SPARTAN FIRE — SPARTAN FIRE METROSTAR, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V538000·2022-07-26

    E-One Fire Trucks Recalled for Electrical Connection Overheating Risk

    E-One is recalling specific 2019-2022 fire trucks because a loose electrical connection may cause the load center to overheat, increasing fire risk.

    Product
    E-ONE — E-ONE CYCLONE II, TYPHOON, TYPHOON N, CYCLONE N
    Category
    Vehicle
    Distribution
    Distributed nationwide