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.

6101–6125 of 29110

  • SevereFDA (Drugs)·D-0212-2024·2022-09-21

    Banana Boat Clear Sunscreen Spray recalled for benzene contamination

    Edgewell Personal Care Brands is recalling Banana Boat hair & scalp defense Clear Sunscreen Spray SPF 30 due to benzene contamination. The affected product was distributed nationwide in the United States.

    Product
    Banana Boat hair & scalp defense, Clear Sunscreen Spray SPF 30, Avobenzone 2.0%, Homosalate 6.0%, Octocrylene 6.0%, packaged in Net Wt 6 oz. aluminum spray can, Distributed by: Edgewell Personal Care Brands, LLC, Shelton, CT 06484, UPC 0 79656 04041 8
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1505-2022·2022-09-21

    Magnesium Citrate Laxative Recalled Due to Microbial Contamination

    Vi-Jon's Magnesium Citrate oral solution laxative is recalled nationwide due to microbial contamination. Approximately 8,682 bottles are affected.

    Product
    MAGNESIUM CITRATE — MAGNESIUM CITRATE (MAGNESIUM CITRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1725-2022·2022-09-21

    Shrimp Tempura Sushi Rolls Recalled for Undeclared Egg and Wheat

    EZ Noble Sushi is recalling Shrimp Tempura and spice shrimp rolls (11.2 oz, expiration 08/12/2022) due to undeclared egg and wheat allergens. Consumers with allergies to eggs or wheat should not consume this product.

    Product
    Shrimp Tempura and spice shrimp roll (11.2 oz) with expiration 08/12/2022
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-1510-2022·2022-09-21

    Walgreens Magnesium Citrate Laxative Recalled for Microbial Contamination

    Walgreens Dye-Free Magnesium Citrate Saline Laxative is recalled nationwide due to microbial contamination affecting certain lots. Consumers should stop using the product immediately.

    Product
    Walgreens, Dye-Free, Magnesium Citrate, SALINE LAXATIVE, Oral Solution, (1.745 g/fl oz), Grape Flavor, 10 FL OZ (296 mL), Distributed By: Walgreen Co., 200 Wilmot RD., Deerfield, IL 60015; NDC 0363-7162-38 UPC 3 11917 20159 7 (purple label).
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1653-2022·2022-09-21

    Baxter CLEARLINK System Non-DEHP Solution Set recalled due to leak reports

    Baxter Healthcare Corporation is recalling the CLEARLINK System Non-DEHP Solution Set nationwide due to increased customer reports of leaks in the in-line injection site device.

    Product
    Baxter CLEARLINK System, Non-DEHP Solution Set with DUO-VENT Spike, Product Code 2R8403. An in-line injection site.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1726-2022·2022-09-21

    Spicy salmon rolls recalled for undeclared egg allergen

    EZ Noble Sushi recalls spicy salmon rolls (9.6 oz, expiration 08/12/2022) sold in MA and CT due to undeclared egg allergen.

    Product
    Spicy salmon roll (9.6 oz) with expiration 08/12/2022
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-1730-2022·2022-09-21

    EZ Noble Sushi Rolls Recalled for Undeclared Egg Allergen

    EZ Noble Sushi is recalling Pink Lady and Salmon Avocado rolls (9 oz, expiration 08/12/2022) distributed in MA and CT due to undeclared egg. Consumers with egg allergies should not consume this product.

    Product
    Pink lady and salmon avocado roll (9 oz) with expiration 08/12/2022
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-1731-2022·2022-09-21

    Shrimp tempura and lobster roll recalled for undeclared wheat allergen

    EZ Noble Sushi is recalling shrimp tempura and lobster roll products with expiration date 08/12/2022 distributed in Massachusetts and Connecticut due to undeclared wheat allergen.

    Product
    Shrimp tempura & lobster roll (12.8 oz) with expiration 08/12/2022
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-1502-2022·2022-09-21

    FDA Recalls CITROMA Magnesium Citrate for Microbial Contamination

    Vi-Jon, LLC is recalling CITROMA magnesium citrate oral laxative solution due to microbial contamination. The affected product was distributed nationwide in the USA, Canada, and Panama.

    Product
    CITROMA — CITROMA (MAGNESIUM CITRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1733-2022·2022-09-21

    GFB Gluten Free Bites Dark Chocolate and Coconut recalled for undeclared cashews

    West Thomas Partners is recalling The GFB Gluten Free Bites Dark Chocolate and Coconut (UPC 856818008895) because the product contains undeclared cashews. Consumers with cashew allergies should not consume this product.

    Product
    The GFB Gluten Free Bites Dark Chocolate and Coconut 1.2oz. UPC 856818008895, 10 retail units per tray, 6 trays per wholesale case.
    Category
    Food
    Distribution
    25 states
  • SevereNHTSA·22E078000·2022-09-20

    ZF Recalls Integrated Pedal Units Due to Brake Pedal Detachment Risk

    ZF North America is recalling Integrated Pedal Units where a missing or loose shaft locking screw could cause the brake pedal to detach, increasing crash risk.

    Product
    SERVICE BRAKES, HYDRAULIC:PEDALS AND LINKAGES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V700000·2022-09-19

    Liquid Transport Recalls 2022 Hays-LTI PTNTT Trailers for Hub Defect

    Liquid Transport is recalling 2022 Hays-LTI PTNTT trailers because a bearing washer may crack, causing the hub to separate from the axle and increasing crash risk.

    Product
    HAYS — HAYS LTI PTNTT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·032-2022·2022-09-17

    Healthy Choice Korean-Style Beef Recalled For Undeclared Milk Allergen

    USDA recalls 22,061 pounds of Healthy Choice Korean-Style Beef due to undeclared milk and misbranding. No illnesses reported.

    Product
    VICS Acquisition, LLC — Valley International Cold Storage Acquisition, LLC, Recalls Frozen Beef Products Due To Misbranding And Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V697000·2022-09-16

    Autocar Recalls 2022 Xpeditor Trucks Due to Tie Rod Clamp Defect

    Autocar is recalling 236 2022 Xpeditor trucks because improperly heat-treated tie rod clamps may fail, causing tie rods to separate and increasing crash risk.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V693000·2022-09-15

    2021 Nissan Versa and Kicks power steering sensor defect

    Nissan is recalling 2021 Versa and Kicks vehicles because an intermittent electrical connection in the power steering torque sensor can disable power steering assist, increasing steering effort and crash risk.

    Product
    NISSAN — NISSAN KICKS, VERSA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V692000·2022-09-15

    Micro Bird Recalls 2018-2019 G5 Electric School Buses for Fire Risk

    Micro Bird is recalling 2018-2019 G5 electric school buses because improperly crimped wires in the charging port may overheat and cause a fire.

    Product
    MICRO BIRD — MICRO BIRD G5 TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V689000·2022-09-14

    Nikola Recalls 2022 Tre BEV Vehicles Due to Seat Belt Anchor Defect

    Nikola is recalling 2022 Tre BEV vehicles because improperly installed seat belt shoulder anchorages may detach during a crash, increasing injury risk.

    Product
    NIKOLA — NIKOLA TRE BEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V684000·2022-09-14

    Ford Recalls 2022 F-150 Trucks for Air Bag Cover Defect

    Ford is recalling 2022 F-150 vehicles because a defective instrument panel cover may cause the air bag to deploy improperly or project fragments.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1657-2022·2022-09-14

    Philips OmniLab Advanced+ sleep apnea devices recalled for off-gassing

    Philips Respironics is recalling 85 units of the OmniLab Advanced+ ventilation device due to motor assemblies containing nonconforming plastic that off-gasses volatile organic compounds.

    Product
    Philips OmniLab Advanced+, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insufficiency.
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-1654-2022·2022-09-14

    Philips BiPAP A30 respiratory device motor assemblies recalled for VOC off-gassing

    Philips Respironics recalls Philips BiPAP A30 respiratory devices due to motor assemblies with nonconforming plastic that off-gases volatile organic compounds (VOCs). Patients should contact the manufacturer immediately.

    Product
    Philips BiPAP A30, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insufficiency.
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Drugs)·D-1478-2022·2022-09-14

    Antacid Medication Recalled Nationwide for Microbial Contamination Risk

    Plastikon Healthcare LLC is recalling 220,500 cups of antacid containing magnesium hydroxide and aluminum hydroxide due to microbial contamination.

    Product
    Magnesium Hydroxide 1200 mg, Aluminum Hydroxide 1200 mg, Simethicone 120 mg per 30 mL, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0904-6838-73
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1659-2022·2022-09-14

    Philips OmniLab ventilator recalled for motor assembly plastic off-gassing defect

    Philips Respironics is recalling OmniLab Advanced + ventilators due to motor assemblies manufactured with nonconforming plastic that releases volatile organic compounds (VOCs). The 8 affected units were distributed across the US and internationally.

    Product
    Philips OmniLab Advanced + with Heated Tube Humidifier, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insufficiency.
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-1656-2022·2022-09-14

    Philips BiPAP V30 Auto Respirators Recalled for VOC Off-Gassing Risk

    Philips Respironics recalls 295 BiPAP V30 Auto respiratory devices due to motor assemblies with nonconforming plastic. These assemblies off-gas volatile organic compounds (VOCs) during device operation.

    Product
    Philips BiPAP V30 Auto, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insufficiency.
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Drugs)·D-1479-2022·2022-09-14

    Antacid Oral Suspension Recalled Nationwide for Microbial Contamination

    Plastikon Healthcare LLC is recalling an antacid oral suspension distributed nationwide due to microbial contamination. Affected lots 20051A (exp. Aug. 2022) and 20088A (exp. Sep. 2022) should not be used.

    Product
    Magnesium Hydroxide 2400 mg, Aluminum Hydroxide 2400 mg, Simethicone 240 mg MAX, per 30 mL Oral Suspension, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC
    Category
    Drug
    Distribution
    Distributed nationwide