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.

1476–1500 of 29080

  • SevereFDA (Food)·H-0215-2025·2025-07-16

    Weaver bulk semi-sweet chocolate nonpareils recalled over undeclared milk allergen

    Weaver Chocolates Nonpareil Semi-Sweet Chocolate in 25 lb bulk cases is being recalled because of an undeclared milk allergen. 849 cases are affected.

    Product
    Weaver Chocolates, 47518 - Nonpareil, Semi-Sweet Chocolate (Christmas Seeds) - 25 lbs. Bulk Cases
    Category
    Food
    Distribution
    14 states
  • SevereFDA (Food)·H-0221-2025·2025-07-16

    Whole organic celery seed recalled over potential Salmonella contamination

    Whole Organic Celery Seed is being recalled because of potential contamination with Salmonella. 439 bags totalling 24,694 lbs are affected.

    Product
    Celery Seed Whole Organic, labeled, "CELERY SEED WHL OG; Net Wt: 56.25 Lbs"
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2083-2025·2025-07-16

    FEM-FLEX II femoral arterial cannulas may have wire protruding from body

    Edwards FEM-FLEX II Femoral Arterial Cannulas are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the outside of the cannula body. 847 units affected.

    Product
    Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII016AS Software Version: N/A Product Description: The Edwards FEMFLEXII Femoral Perfusion Cannluae provides or establishes arterial perfusion in the extracorporeal circuit for d 6 hours.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2081-2025·2025-07-16

    Optisite OPTI18 arterial cannulas may have wire protruding from the body

    Edwards Optisite OPTI18 Arterial Cannulas are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the outside of the cannula body. 13,240 units affected.

    Product
    Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial Cannula Model/Catalog Number: OPTI18 Software Version: N/A Product Description: Cardiac cannula. The Edwards OptiSite Arterial Perfusion Cannluae provides or establishes arterial perfusion in the extracorpo
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2047-2025·2025-07-16

    Bravo CF capsule delivery devices may have misapplied adhesive causing malfunction

    The Bravo CF capsule delivery device is being recalled because misapplied adhesive may prevent the pH capsule attaching to the oesophagus or detaching from the delivery device. 128,202 units affected.

    Product
    Bravo CF capsule delivery device, designed to place and attach a pH monitoring capsule to the esophagus using endoscopic or manometric guidance, Product Number FGS-0635 (5 pack) and FGS-0636 (1 pack)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2032-2025·2025-07-16

    Hillrom LikoScale patient lift components may falsely latch and detach

    Hillrom LikoScale components used with patient lift adapter kits are being recalled because the Q-link 13 may allow false latching of the quick-release hook. 9,839 units are affected.

    Product
    Hillrom LikoScale component, Product Code 3156232, used with the following adapter kits for patient lifts: 1) LikoScale 200 Accessory - Product Code 3156225; 2) LikoScale 350 Accessory - Product Code 3156228; 3) LikoScale 400 Accessory - Product Code 3156226.
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·25V415000·2025-07-15

    Porsche suspension strut retaining ring can loosen dislodging the strut

    Porsche is recalling certain 2025 Panamera, Panamera E-Hybrid and Taycan vehicles because a retaining ring on top of the suspension strut may come loose, dislodging the strut and losing air from the spring.

    Product
    PORSCHE — PORSCHE TAYCAN, PANAMERA, PANAMERA 4 E-HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V468000·2025-07-14

    AMO Recalls 2025 Utility Trailers Due to Axle Separation Risk

    American Manufacturing Operations is recalling 2025 AMO Utility trailers because shackle nuts may loosen, allowing the axle to detach and increasing crash risk.

    Product
    AMO — AMO UTILITY TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V459000·2025-07-11

    Zero Motorcycles Recalls 2024 Models Due to Front Brake Hose Defect

    Zero Motorcycles is recalling 2024 DSR/X, DS, DSR, and DSRP motorcycles because a twisted front brake hose may leak fluid and reduce braking ability.

    Product
    ZERO — ZERO DSRP, DSR, DS, DSR/X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V467000·2025-07-11

    Ford Bronco Sport and Escape fuel injectors may crack and leak

    Ford is recalling certain 2021-2024 Bronco Sport and 2020-2022 Escape vehicles with 1.5L engines because a fuel injector may crack and leak fuel inside the engine compartment. 694,271 vehicles affected.

    Product
    FORD — FORD BRONCO SPORT, ESCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25377·2025-07-10

    Ozark Trail 64 ounce water bottle lids can forcefully eject

    Ozark Trail 64 oz Stainless Steel Insulated Water Bottles are being recalled because the lid can forcefully eject on opening. Three injuries are reported, including two cases of permanent vision loss.

    Product
    Ozark Trail 64 oz Stainless Steel Insulated Water Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V462000·2025-07-10

    Mitsubishi Fuso Rizon Trucks Recalled for Electric Parking Brake Fire Risk

    Mitsubishi Fuso is recalling 2024-2025 Rizon trucks because an oversized spacer in the electric parking brake may cause overheating and fire.

    Product
    MITSUBISHI FUSO — MITSUBISHI FUSO RIZON FEC7K (E16), RIZON FEC9K (E18), RIZON FECXK (E18)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0164-2025·2025-07-09

    ZENSHI Handcrafted Sushi Happy Heart Platter recalled for Salmonella

    Harris Teeter is recalling ZENSHI Handcrafted Sushi Happy Heart Platter #3 (Crunchy Dragon Tempura) because recalled cucumbers used in the product may contain Salmonella.

    Product
    ZENSHI HANDCRAFTED SUSHI Happy Heart Platter #3 (Crunchy Dragon Tempura) 20pc Net Wt. 23.9oz UPC 0 23012 94362 2
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·H-0140-2025·2025-07-09

    Harris Teeter ZENSHI Handcrafted Sushi Crunchy Dragon Roll Recalled for Salmonella

    Harris Teeter is recalling ZENSHI HANDCRAFTED SUSHI Crunchy Dragon Roll (10pc, 9.6oz) due to possible Salmonella contamination from recalled cucumbers used in the product.

    Product
    ZENSHI HANDCRAFTED SUSHI Crunchy Dragon Roll 10pc Net Wt. 9.6oz UPC 0 23012 94461 2
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·H-0192-2025·2025-07-09

    Harris Teeter ZENSHI Handcrafted Sushi Spicy Roll Tuna Salmonella Recall

    Harris Teeter is recalling ZENSHI HANDCRAFTED SUSHI Spicy Roll - Tuna 10pc (Brown Rice) due to possible Salmonella contamination from recalled cucumbers used in the product.

    Product
    ZENSHI HANDCRAFTED SUSHI Spicy Roll - Tuna 10pc (Brown Rice) Net Wt. 7.1oz UPC 0 23012 94319 6 & UPC 0 23012 95149 8
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·H-0185-2025·2025-07-09

    Zenshi spicy California brown rice rolls made with recalled cucumbers

    Zenshi Handcrafted Sushi Spicy California Roll on brown rice is being recalled over cucumbers recalled for possible Salmonella. 4,906 trays are affected.

    Product
    ZENSHI HANDCRAFTED SUSHI Spicy California Roll 10pc (Brown Rice) Net Wt. 7.4oz UPC 0 23012 94405 6 & UPC 0 23012 95145 0
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·H-0187-2025·2025-07-09

    ZENSHI Handcrafted Sushi Spicy Roll Salmon recalled for Salmonella

    Harris Teeter is recalling ZENSHI Handcrafted Sushi Spicy Roll - Salmon 10pc due to possible Salmonella contamination from recalled cucumbers used in the product.

    Product
    ZENSHI HANDCRAFTED SUSHI Spicy Roll - Salmon 10pc Net Wt. 7.1oz UPC 0 23012 94312 7 & 0 23012 95148 1
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·H-0172-2025·2025-07-09

    Zenshi hybrid Ni sushi platters made with recalled cucumbers

    Zenshi Handcrafted Sushi Hybrid Ni Platter is being recalled because it was made with cucumbers recalled over possible Salmonella. 7 trays are affected.

    Product
    ZENSHI HANDCRAFTED SUSHI Hybrid Ni Platter 31pc Net Wt. 33.1oz UPC 0 23012 94258 8
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Drugs)·D-0504-2025·2025-07-09

    Zicam cold remedy nasal swabs recalled over fungal contamination

    Zicam Cold Remedy Medicated Nasal Swabs are being recalled because of fungal contamination of the swabs. All lots are affected, covering 3,374,918 cartons.

    Product
    ZICAM COLD REMEDY MEDICATED NASAL SWABS, 20 Single-Use Swabs per carton, Distributed by Church & Dwight Co,. Inc., Ewing NJ. UPC 7 32216 30120 5
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2015-2025·2025-07-09

    Servo-u MR Ventilator System inaccurate patient circuit compliance measurement

    Servo-u MR Ventilator System (Model 6888800) may measure patient circuit compliance inaccurately due to incorrect pre-use leakage testing and incorrect active humidifier use.

    Product
    Servo-u MR Ventilator System. Model Number: 6888800.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0165-2025·2025-07-09

    Zenshi Hawaiian roll sushi trays made with recalled cucumbers

    Zenshi Handcrafted Sushi Hawaiian Roll is being recalled because it was made with cucumbers recalled over possible Salmonella. 1,269 trays are affected.

    Product
    ZENSHI HANDCRAFTED SUSHI Hawaiian Roll 10pc Net Wt. 11.0oz UPC 0 23012 94363 9
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·H-0145-2025·2025-07-09

    Zenshi crunchy shrimp roll trays made with recalled cucumbers

    Zenshi Handcrafted Sushi Crunchy Roll with shrimp is being recalled over cucumbers recalled for possible Salmonella. 6,523 trays are affected.

    Product
    ZENSHI HANDCRAFTED SUSHI Crunchy Roll - Shrimp 10pc Net Wt 10.0oz UPC 0 23012 95042 2
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·H-0158-2025·2025-07-09

    Zenshi spicy tuna and rainbow duo combo used recalled cucumbers

    Zenshi Handcrafted Sushi Duo Combo with Spicy Tuna and Rainbow Roll is being recalled over cucumbers recalled for possible Salmonella. 6,986 trays are affected.

    Product
    ZENSHI HANDCRAFTED SUSHI Duo Combo - Spicy Tuna & Rainbow Roll 10pc Net Wt 8.1oz UPC 0 23012 94208 3
    Category
    Food
    Distribution
    8 states