The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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7226–7250 of 36565

  • SevereFDA (Drugs)·D-1501-2022·2022-09-21

    Equate Magnesium Citrate Saline Laxative Recalled Due to Microbial Contamination

    Equate Magnesium Citrate saline laxative has been recalled for microbial contamination. The FDA Class I recall affects 18,324 bottles distributed in the US, Canada, and Panama.

    Product
    equate Magnesium Citrate, SALINE LAXATIVE, (1.745g/fl oz) 10 FL OZ (296mL), Grape Flavor, Distributed By: Walmart, Inc. Bentonville, AR 72716; NDC 49035-592-38 UPC 6 81131 28715 9
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V706000·2022-09-21

    Mack Recalls One 2021 LR Electric Truck for Battery Fire Risk

    Mack Trucks is recalling one 2021 LR Electric truck because a coolant line may not be fully seated, creating a risk of electrical short circuit and fire.

    Product
    MACK — MACK LR ELECTRIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • 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
  • CriticalFDA (Drugs)·D-1476-2022·2022-09-14

    Milk of Magnesia Recalled Nationwide for Microbial Contamination

    Plastikon Healthcare LLC has recalled Milk of Magnesia USP nationwide due to microbial contamination in non-sterile products. The affected lot (20071A) included approximately 24,400 institutional-use cups.

    Product
    MILK OF MAGNESIA USP, 2400 mg/30 mL, Magnesium Hydroxide, 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 0904-6846-73.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1690-2022·2022-09-14

    Select Bakery Cheese Streusel Supreme Recalled for Undeclared Walnuts and Food Colorants

    Select Bakery Cheese Streusel Supreme is recalled due to undeclared walnuts and food colorants. Consumers with allergies or sensitivities to walnuts, Yellow #5, Yellow #6, or Red #40 should not consume this product.

    Product
    Select Bakery Cheese Streusel Supreme Net Wt. 3 Oz (85g) Select Bakery, Inc., Rockwell, N.C. 28138 UPC 0 28598 10054 4
    Category
    Food
    Distribution
    3 states
  • CriticalCPSC·22221·2022-09-14

    ThyssenKrupp Residential Elevators Recalled Due to Child Entrapment Hazard

    ThyssenKrupp Access Corp. is recalling about 16,800 residential elevators sold between 1996 and 2012 due to an entrapment hazard. Children can become trapped in the gap between exterior and interior doors, resulting in serious injury or death; one child death has been reported.

    Product
    thyssenkrupp Access Corp. Residential Elevators
    Category
    Consumer Product
    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
  • SevereNHTSA·22V688000·2022-09-14

    Thomas Built Saf-T-Liner HDX School Buses Recalled for Panel Joint Strength

    Daimler Trucks North America is recalling 2020-2023 Thomas Built Saf-T-Liner HDX school buses because rear side-body panels may have insufficient joint strength.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • 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
  • 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 (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-1658-2022·2022-09-14

    Philips OmniLab Advanced+ Ventilation Devices Recalled for Plastic Off-Gassing

    Philips Respironics is recalling certain Philips OmniLab Advanced+ noninvasive ventilation devices due to motor assemblies with nonconforming plastic that can off-gas volatile organic compounds (VOCs). This is an FDA Class I recall.

    Product
    Philips OmniLab Advanced+ Intl (Flow Gen), 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-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
  • 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
  • SevereFDA (Food)·F-1691-2022·2022-09-14

    Select Bakery Brownie Recall: Undeclared Walnuts and Red #40

    Select Bakery Chocolate Chip Brownies (3 oz) are recalled due to undeclared walnuts and Red #40. Product was distributed to Georgia, North Carolina, and South Carolina.

    Product
    Select Bakery CHOCOLATE CHIP BROWNIE Net Wt. 3 Oz (85g) Contains: Wheat, Milk, Soy and Egg ingredients. Select Bakery, Inc., Rockwell, N.C. 28138 UPC 0 28598 10025 4
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-1477-2022·2022-09-14

    Milk of Magnesia USP Recalled for Microbial Contamination Nationwide

    Plastikon Healthcare LLC is recalling Milk of Magnesia USP due to microbial contamination in non-sterile products. Lot 20074A, distributed nationwide for institutional use, should not be used.

    Product
    MILK OF MAGNESIA USP, 2400 mg/10 mL, Magnesium Hydroxide, 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 0904-6840-72.
    Category
    Drug
    Distribution
    Distributed nationwide
  • 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