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.

Filters

Agency

Category

Minimum severity

Clear filters

601–625 of 36488

  • SevereNHTSA·26V371000·2026-06-09

    Ford Recalls 2024 Explorers for Potential Park System Damage

    Ford is recalling 2024 Explorer vehicles with 2.3L engines and 10R60 transmissions because an unintentional powertrain control module reset may damage the park system, increasing the risk of vehicle rollaway.

    Product
    FORD — FORD EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E033000·2026-06-09

    Cummins CNG Fuel System Recall for Tank Bracket Deformation Risk

    Natural Gas Fuel Systems is recalling Cummins CNG fuel systems because the tank support bracket may deform in a side impact, potentially causing the tank to detach and leak fuel.

    Product
    FUEL SYSTEM, OTHER:STORAGE:TANK ASSEMBLY:MOUNTING recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26529·2026-06-04

    Pool Drain Covers Recalled for Entrapment and Drowning Hazards

    Broqixin pool drain covers violate federal safety standards and pose a risk of serious injury or death from entrapment and drowning. About 370 units sold on Amazon from January to April 2026 should be removed immediately.

    Product
    Broqixin Pool Drain Covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26532·2026-06-04

    Vornado SRTH Small Room Tower Heaters Recalled for Fire Hazard

    Vornado is recalling about 255,000 SRTH small room tower heaters because the fan blade can detach, causing overheating and fire. Vornado has received 32 overheating reports, including eight fires and one smoke inhalation.

    Product
    SRTH Small Room Tower Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26527·2026-06-04

    Crenlux Pool Drain Covers Recalled for Entrapment and Drowning Hazards

    Crenlux pool drain covers violate federal safety standards and pose risks of entrapment and drowning. About 200 units sold on Amazon from June 2025 through March 2026 are affected.

    Product
    Crenlux Pool Drain Covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26524·2026-06-04

    Wyze Solar Cam Pan Security Cameras recalled for fire and burn hazard

    Wyze Labs is recalling about 321,360 Solar Cam Pan security cameras because incorrect assembly instructions can cause the lithium-ion battery to overheat and catch fire. The firm has received 13 reports of overheating, six of fires, and six reports of minor burns.

    Product
    Wyze Solar Cam Pan Security Cameras
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26531·2026-06-04

    Residential Elevator Interlock Switches Recalled for Fall and Crushing Hazard

    SUNS International is recalling about 7,000 SS6291 Solenoid Interlock Switches used in residential elevators because they can become stuck, allowing the exterior door to remain unlocked and creating a risk of death or serious injury.

    Product
    SUNS SS6291 Solenoid Interlock Switches
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26525·2026-06-04

    Little Grape Land Nursing Pillows Recalled Due to Suffocation Risk

    Little Grape Land Nursing Pillows are being recalled due to a risk of serious injury or death from suffocation. The pillows violate mandatory safety standards for nursing pillows and infant support cushions. No injuries have been reported.

    Product
    Little Grape Land Nursing Pillows
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V363000·2026-06-04

    Jeep Recalls Wrangler and Gladiator Models Due to Fire Risk

    Chrysler is recalling 2021-2025 Jeep Wrangler and Gladiator vehicles because steering pump wiring may overheat and cause a fire.

    Product
    JEEP — JEEP WRANGLER 4XE, GLADIATOR, WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2235-2026·2026-06-03

    Medline Spinal Block Kits Recalled Due to Quality and Efficacy Concerns

    Medline Industries, LP is recalling Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection due to microbiology testing data integrity concerns and efficacy complaints.

    Product
    Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: SPINAL BLOCK 22G QUINCKE 5S BU, Medline Kit SKU DYNJRA9026
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2234-2026·2026-06-03

    Medline Kits Containing Bupivacaine Hydrochloride Recalled Due to Quality and Efficacy Concerns

    Medline Industries, LP is recalling specific Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection due to microbiology testing data integrity concerns and efficacy complaints.

    Product
    Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) BLOCK TRAY, Medline Kit SKU DYNJRA1181C; 2) SPINAL BLOCK 25G WHTCRE 5S BU, Medline Kit SKu DYNJRA1860.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2237-2026·2026-06-03

    Medline spinal anesthesia trays recalled over Huons bupivacaine quality concerns

    Medline spinal anesthesia trays containing Huons Bupivacaine HCl in Dextrose Injection are being recalled after that drug was recalled. 200,702 kits are affected.

    Product
    Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL ANESTHESIA TRAY-LF, Medline Kit SKU DYNJRA0102A; 2) SPINAL TRAY-LF, Medline Kit SKU DYNJRA0143B; 3) SPINAL PREP TRAY-LF, Medline Kit SKU DYNJRA0205B; 4) SPINAL TRAY, Medline Ki
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0849-2026·2026-06-03

    Bulk banana smoothie base made with potentially Salmonella-contaminated ingredient

    A bulk banana smoothie base is being recalled because the firm received and used a potentially Salmonella-contaminated ingredient to manufacture various products. 4,980 pounds are affected.

    Product
    (BULK) SPL-BEV Banana CWT (Banana Smoothie); Super Sack Tote Item# 355-0099
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-2238-2026·2026-06-03

    Automated Impella Controllers recalled over alarm, power and purge cassette faults

    Automated Impella Controllers sold outside the US are being recalled over alarm failures, power-path faults, electrical-short risks, inaccurate motor-current sensing and purge cassette misalignment.

    Product
    Automated Impella Controller (AIC) with the below product descriptions and corresponding Product Codes. 1. Impella Controller, Packaged, CA; Product Code: 0042-0000-CA. 2. Impella Controller, Packaged, EU; Product Code: 0042-0000-EU. 3. Impella Controller, Packaged, UK
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2233-2026·2026-06-03

    Medline spinal trays recalled over Huons bupivacaine quality concerns

    Medline spinal trays containing Huons Bupivacaine HCl in Dextrose Injection are being recalled after that drug was recalled over microbiology data integrity and efficacy complaints.

    Product
    Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL TRAY W/PENCIL POINT NDL, Medline Kit SKU DYNJRA0245; 2) SPINAL TRAY W/PENCIL POINT NDL, Medline Kit SKU DYNJRA0555; 3) SPINAL TRAY, Medline Kit SKU DYNJRA0836A; 4) SPINAL T
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0857-2026·2026-06-03

    Wawa diet lemonade pints recalled over undeclared milk allergen

    Wawa Diet Lemonade in 16 oz plastic bottles is being recalled because of an undeclared milk allergen. 374 units are affected.

    Product
    Wawa Diet Lemonade Pint (16oz), Plastic bottle
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Devices)·Z-2232-2026·2026-06-03

    Medline pain and Whitacre spinal trays recalled over bupivacaine concerns

    Medline pain trays and Whitacre spinal block trays containing Huons Bupivacaine HCl in Dextrose Injection are being recalled after that drug was recalled. 28,106 kits are affected.

    Product
    Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) PAIN TRAY, Medline Kit SKU DYNJRA1555; 2) SPINAL BLOCK TRAY WHITACRE 24G, Medline Kit SKU DYNJRA1817; 3) TRAY, 25G WHIT SPINAL W/PHARM, Medline Kit SKU DYNJRA1920; 4) ULTRASOUND
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0852-2026·2026-06-03

    Giant Eagle pita chips made with recalled California Dairies milk powder

    Giant Eagle Baked Pita Chips with Parmesan, Garlic & Herb Bagel Crisps are being recalled because they were made with recalled California Dairies milk powder over Salmonella.

    Product
    giant eagle Baked Pita Chips with Parmesan, Garlic & Herb Bagel Crisps, Net Wt 7.33 oz. Shipping Case: 12 ct - 7.33 oz Bags Net Weight: 5.49 lbs. Legacy Bakehouse, LLC, Waukesha WI 53186.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-2236-2026·2026-06-03

    Medline spinal block trays recalled over Huons bupivacaine quality concerns

    Medline spinal block trays containing Huons Bupivacaine HCl in Dextrose Injection are being recalled after that drug was recalled. 30,120 kits are affected.

    Product
    Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL BLOCK TRAY, Medline Kit SKU DYNJRA1097; 2) TRAY, SPINAL PENCIL POINT 25G, Medline Kit SKU DYNJRA1154; 3) SPINAL TRAY, Medline Kit SKU DYNJRA1192A; 4) BLOCK TRAY, Medline
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2211-2026·2026-06-03

    Automated Impella Controllers await four pending hardware safety updates

    Automated Impella Controllers that have not been through Abiomed's servicing process are pending four hardware updates addressing motor control, startup and pump stop risks.

    Product
    Automated Impella Controller (AIC); Product Code: 0042-0000-US;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2160-2026·2026-06-03

    RelayPro thoracic stent-graft clasp may not release from delivery system

    The RelayPro Thoracic Stent-Graft System is subject to a labeling update concerning proximal clasp disconnection from the outer control tube, which may prevent release of the graft.

    Product
    RelayPro Thoracic Stent-Graft System (various sizes) Reference numbers: 28-N4-32-104-32U 28-N4-32-164-28U 28-N4-32-164-32U 28-N4-32-209-28U 28-N4-32-209-32U 28-N4-32-259-32U 28-N4-34-109-34U 28-N4-34-154-30U 28-N4-34-154-34U 28-N4-34-209-30U 28-N4-34-209-34U 28-N4-34-259-34U 28-
    Category
    Medical Device
    Distribution
    1 state