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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2351–2375 of 36523

  • SevereFDA (Food)·H-0021-2025·2025-06-18

    Sysco Created Fresh Tuna Salad Subs Recalled for Salmonella Risk

    Sysco Corporation is recalling Created Fresh Sub-Tuna Salad on Everything Ficelle (5.76 oz.) due to potential Salmonella contamination from cucumbers used in the product.

    Product
    HKSAN167 1/5.76 OZ. EA CREATED FRESH Sub- Tuna Salad on Everything Ficelle ALL LOT CODES HKSAN167 1/5.76 OZ. EA Created Fresh Sub- Tuna Salad on Everything Ficelle ALL LOT CODES
    Category
    Food
    Distribution
    18 states
  • SevereFDA (Food)·H-0039-2025·2025-06-18

    Cucumber and Grape Tomato Product Recalled for Salmonella Contamination

    TGD Cuts, LLC is recalling Cucumber Sliced/Grape Tomato 50/2oz. packs due to Salmonella contamination. The affected product was distributed to Maryland, Pennsylvania, North Carolina, Virginia, and New Jersey.

    Product
    Cucumber Sliced/Grape Tomato 50/2oz. Pack, 50 per case
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·H-0026-2025·2025-06-18

    Cucumbers Recalled Due to Potential Salmonella Contamination

    Lipman Family Farms is recalling 24-count repacked cucumbers distributed across 18 states due to potential Salmonella contamination. Consumers should not consume the product and should discard or return affected cucumbers.

    Product
    Cucumber 24 Ct Repacked by Lipman Produce Hendersonville, NC 28792, Product of USA
    Category
    Food
    Distribution
    18 states
  • SevereFDA (Food)·H-0034-2025·2025-06-18

    Jean's Classy Fresh Salsa Mild recalled for Salmonella contamination

    TGD Cuts, LLC is recalling Jean's Classy Fresh Salsa, Mild (5 lbs.) due to Salmonella contamination. The product was distributed to Maryland, Pennsylvania, North Carolina, Virginia, and New Jersey.

    Product
    Jean's Classy Fresh Salsa, Salsa, Mild 5 lbs. 1 per case .
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·H-0029-2025·2025-06-18

    Lipman Family Farms Sliced Cucumbers Recalled for Potential Salmonella

    Lipman Family Farms is recalling sliced cucumbers due to potential Salmonella contamination. The product was distributed across multiple states, and consumers should not consume it.

    Product
    PR Cucumber Sliced 2/5# 1/4 Pack Date May 22 Product of USA Lipman Family Farms Hendersonville / NC
    Category
    Food
    Distribution
    18 states
  • SevereFDA (Food)·H-0031-2025·2025-06-18

    Smartcuts Cucumber Sliced Trays recalled due to Salmonella contamination

    Smartcuts Cucumber Sliced Trays 2/2lb have been recalled because they may be contaminated with Salmonella. Affected lots include F13625, F13825, and F14025 with expiration dates from 05/25 to 05/29.

    Product
    Smartcuts Cucumber Sliced Trays 2/2lb
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1865-2025·2025-06-18

    Z-800 Infusion System recalled for unverified software installation

    Zyno Medical LLC is recalling 613 units of the Z-800 Infusion System distributed nationwide because unreleased software versions were installed on the devices without verification or validation.

    Product
    Z-800 Infusion System. Intended to provide intravenous infusion of parenteral fluids, blood, and blood products to a patient.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1929-2025·2025-06-18

    Philips Intera 1.5T Achieva IT Nova MRI System Gradient Coil Fire Risk

    Philips is recalling one Intera 1.5T Achieva IT Nova MRI system due to a gradient coil component that may overheat and produce smoke or fire, posing risks of inhalation injury, burns, or death.

    Product
    Intera 1.5T Achieva IT Nova Product Number: 781175
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0459-2025·2025-06-18

    Celecoxib Capsules 200 mg recalled for foreign tablets inside bottles

    Alembic Pharmaceuticals is recalling Celecoxib 200 mg capsules after a customer found a Tadalafil 5 mg tablet inside a sealed 500-count bottle. The contamination was discovered through a customer complaint.

    Product
    Celecoxib Capsules, 200 mg, 500-count bottle, Rx only, Manufactured by: Alembic Pharmaceuticals Limited (Formulation Division), Panelav 389350, Gujarat, India, Manufactured for: Alembic Pharmaceuticals, Inc., Bedminster, NJ 07921, USA, NDC 62332-142-71
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0488-2025·2025-06-18

    Sulfamethoxazole and Trimethoprim Tablets Recalled for Microbial Contamination

    Amneal Pharmaceuticals is recalling Sulfamethoxazole and Trimethoprim Tablets (400 mg/80 mg) nationwide due to microbial contamination that may cause black spots on tablets. The contamination affects non-sterile products distributed across the USA.

    Product
    SULFAMETHOXAZOLE AND TRIMETHOPRIM — SULFAMETHOXAZOLE AND TRIMETHOPRIM (SULFAMETHOXAZOLE AND TRIMETHOPRIM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0465-2025·2025-06-18

    Dietary Supplement Electro Buzz Recalled for Undeclared Active Pharmaceutical Ingredients

    SAINI TRADE INC is recalling ELECTRO BUZZ dietary supplement (lot KT-1ST-43-01-07/2024, expiring 10/15/2026) distributed nationwide. Laboratory testing found undeclared chloropretadalafil, propoxyphenylsildenafil, and sildenafil.

    Product
    ELECTRO BUZZ, Dietary Supplement, 10 capsules per box, Distributed By: Health Fixer, Tempe, AZ 85288, UPC B0DK68LF6J.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1868-2025·2025-06-18

    Z-800WF Infusion System software verification defect recall

    Zyno Medical LLC is recalling 613 units of the Z-800WF Infusion System because unreleased software versions were installed on distributed devices without verification or validation.

    Product
    Z-800WF Infusion System. Intended to provide intravenous infusion of parenteral fluids, blood, and blood products to a patient.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1931-2025·2025-06-18

    Philips Intera 1.5T Achieva Nova-Dual MRI System Fire Hazard Recall

    Philips is recalling three Intera 1.5T Achieva Nova-Dual MRI systems worldwide due to a gradient coil component failure that can generate smoke and fire, posing risks including burn injury and asphyxia.

    Product
    Intera 1.5T Achieva Nova-Dual Product Number: 781173;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1936-2025·2025-06-18

    Philips SmartPath to dStream 1.5T MRI Gradient Coil Fire Risk

    Philips SmartPath to dStream for 1.5T MRI systems are recalled due to potential gradient coil component failure that may produce smoke and fire, posing risks of inhalation injury, burns, asphyxia, and death.

    Product
    SmartPath to dStream for 1.5T¿; Product Number: 782146;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0463-2025·2025-06-18

    Dietary Supplement Male Ultra Recalled for Undeclared Drug Ingredients

    Male Ultra dietary supplement, distributed nationwide in 3,000 boxes, has been recalled because laboratory testing found it contains undeclared pharmaceutical ingredients: propoxyphenylsildenafil and sildenafil. The product was marketed without FDA approval.

    Product
    Male Ultra, Unleash Your Force, Dietary Supplement,10 capsules per box, Distributed By; Health Fixer, Tempe, AZ 85288, UPC B0CMQ4FTHG.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1924-2025·2025-06-18

    Azure S DR MRI SureScan Pacemakers Recalled for Battery Failure Risk

    Medtronic Azure S DR MRI SureScan pacemakers may experience sudden battery power failure without warning, potentially interrupting therapy and leading to cardiac arrest or hospitalization. Affected devices are being recalled internationally.

    Product
    Azure S DR MRI SureScan, Product number W3DR01
    Category
    Medical Device
    Distribution
    0 states
  • SevereUSDA FSIS·022-2025·2025-06-13

    King Tallow LLC Recalls Beef Tallow Produced Without Federal Inspection

    King Tallow LLC is recalling 353 pounds of beef tallow jars produced without federal inspection. The product was sold in Puerto Rico.

    Product
    King Tallow LLC Recalls Beef Tallow Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·25V394000·2025-06-13

    Ford Recalls 2025 Mustang Mach E for Transmission Park Rod Defect

    Ford is recalling 2025 Mustang Mach E vehicles because the transmission park rod may fail to engage, creating a risk of vehicle rollaway and crash.

    Product
    FORD — FORD MUSTANG MACH E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V401000·2025-06-13

    Ford Super Duty brake pushrod springs missing; owners told not to drive

    Ford is recalling certain 2025 Super Duty trucks because the brake booster pushrod retaining spring may not have been installed, risking sudden loss of brake function.

    Product
    FORD — FORD F-250 SD, F-350 SD, F-450 SD, F-550 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·021-2025·2025-06-12

    Starway Recalls Ineligible Frozen Fish Balls Imported From Vietnam

    Starway International Group is recalling approximately 9,513 pounds of frozen fish balls imported from Vietnam because the producing establishment is not eligible to export to the US.

    Product
    Starway International Group LLC Recalls Ineligible Frozen Siluriformes Fish Ball Products Imported From Vietnam
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V392000·2025-06-12

    Volvo electric and hybrid models can lose braking in one-pedal mode

    Volvo is recalling certain electric and plug-in hybrid models because the vehicle may lose brake function while coasting downhill in "B" mode or One Pedal Drive. Owners are told not to use those modes until repaired.

    Product
    VOLVO — VOLVO XC60PHEV, C40BEV, EC40, EX40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V391000·2025-06-12

    Honda and Acura brake pedal pivot pins may not be secured

    Honda is recalling certain Acura TLX, Acura MDX and Honda Pilot vehicles because the brake pedal pivot pin was not secured properly, which can shift the pedal out of position.

    Product
    ACURA — ACURA, HONDA TLX, MDX, PILOT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25336·2025-06-12

    Bugaboo Giraffe Highchairs Recalled for Fall Hazard Risk

    Bugaboo North America is recalling about 18,280 Giraffe highchairs because the legs can detach from the frame if screws are not properly tightened during assembly, posing a risk of serious injury or death. The company has received 22 reports of leg detachment, including 13 reports of minor injuries.

    Product
    Giraffe highchairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide