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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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

1476–1500 of 26027

  • HighFDA (Devices)·Z-1550-2026·2026-03-18

    APTUS TriLock Screw mix-up between 2.5mm and 2.8mm models

    Medartis AG is recalling certain lots of APTUS 2.8 TriLock Screws due to a mix-up with 2.5mm screws. The dimensional error could affect the fit and stability of orthopedic fixation in hand, forearm, shoulder, and foot surgery.

    Product
    Brand Name: APTUS Product Name: 2.8 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5850.16/1 Software Version: Not applicable. Product Description: The APTUS fixation systems are used for fractures, osteotomies and arthrodesis of the hand, forearm, shoulder and foot.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1522-2026·2026-03-18

    Endo-Model plateau screw implants recalled due to potential bushing failure

    Waldemar Link is recalling Endo-Model Replacement Plateau implants because the bushing could detach from the screw shaft due to a longitudinal fracture. This could compromise implant stability.

    Product
    Endo-Model Replacement Plateau; Item Number: 15-0027/12;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1523-2026·2026-03-18

    Endo-Model Replacement Plateau Orthopedic Implants Recalled for Screw Bushing Detachment

    Waldemar Link is recalling 3 units of Endo-Model Replacement Plateau orthopedic implants due to potential detachment of the bushing from the screw shaft. The defect results from a longitudinal fracture in the screw.

    Product
    Endo-Model Replacement Plateau; Item Number: 15-0027/16;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1517-2026·2026-03-18

    Endo-Model Replacement Plateau Screw Recalled for Bushing Detachment Risk

    Waldemar Link recalls its Endo-Model Replacement Plateau due to potential bushing detachment from the screw shaft, which could cause implant failure. Four units were affected and distributed worldwide.

    Product
    Endo-Model Replacement Plateau; Item Number: 15-8030/12;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1533-2026·2026-03-18

    GEM Premier 5000 Lab Analyzer Cartridges May Eject During Testing

    GEM Premier 5000 lab cartridges may eject repeatedly during warm-up, requiring replacement and potentially delaying patient test results. No illnesses or injuries have been reported.

    Product
    GEM Premier 5000; Part No. 00055415005.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1554-2026·2026-03-18

    Medical augmentation devices recalled for failed bacterial endotoxin testing

    International Life Sciences is recalling Artelon FlexBand Dynamic Matrix augmentation devices due to failed bacterial endotoxin testing. The devices were distributed nationwide and internationally.

    Product
    Artelon FlexBand Dynamic Matrix Ref: 31057
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1525-2026·2026-03-18

    GEM Premier 5000 PAK Cartridges May Eject During Warm-Up

    Instrumentation Laboratory is recalling GEM Premier 5000 PAK cartridges that may experience increased ejection errors during warm-up, potentially delaying laboratory test results.

    Product
    GEM Premier 5000 PAK; Part No. 00055360008.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1542-2026·2026-03-18

    GEM Premier 5000 Cartridges Recalled for Control Solution Detection Errors

    Instrumentation Laboratory is recalling GEM PAK cartridges for the GEM Premier 5000 due to increased failures in process control detection during warm-up, which may cause cartridge ejection and delay laboratory test results.

    Product
    GEM Premier 5000; Part No. 00055445008.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1538-2026·2026-03-18

    GEM Premier 5000 Analyzer Cartridges May Malfunction During Warm-Up

    Instrumentation Laboratory is recalling 74 units of GEM Premier 5000 analyzer cartridges that may malfunction during warm-up, causing cartridge ejection and potentially delaying patient test results.

    Product
    GEM Premier 5000; Part No. 00055430008.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1544-2026·2026-03-18

    Physio-Control Infant and Child Defibrillator Electrodes Recalled for Delamination

    Physio-Control is recalling Infant/Child Reduced Energy Defibrillator Electrodes due to delamination of the electrode material that could affect proper functioning during emergency treatment of pediatric patients.

    Product
    PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Electrodes Catalog Numbers: 11101-000016 UDI-DI code: 00721902629013 Catalog Number: 11101-000017 UDI-DI code: 00721902682483 Infant/Child Reduced Energy Defibrillation Electrodes are pre gelled, self-adhesive, the
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1555-2026·2026-03-18

    Surgical Augmentation Devices Recalled for Bacterial Endotoxin Testing Failure

    International Life Sciences recalls Artelon FlexBand Plus surgical devices (Ref 41054, 41057) worldwide due to bacterial endotoxin contamination discovered during testing.

    Product
    Artelon FlexBand Plus Ref: 41054 & 41057
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0549-2026·2026-03-18

    Hortex Mieszanka 9 Spring Vegetable Mix Recalled for Potential Glass Contamination

    Polski Ogrod Sp. z o.o. is recalling Hortex Mieszanka 9 Spring vegetable mix due to potential glass contamination. The affected product was distributed in Illinois.

    Product
    Hortex Mieszanka 9 - skBadnikowa Spring vegetable mix with 9 ingredients, net wt 15.87oz., UPC 5 900477 018735 >, 14 units per case
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0613-2026·2026-03-18

    CNC Noodle Corporation Steam Noodles Recalled for Undeclared Wheat

    CNC Noodle Corporation is recalling China Noodle Co. Steam Noodle packages due to undeclared wheat in the product, which poses a risk to consumers with wheat allergies.

    Product
    Secondary Packaging: STEAM NOODLES INGREDIENTS: ENRICHED FLOUR, WATER, STARCH, SALT, POTASSIUM, CARBONATE AND BENZOATE OF SODA ADDED AS PRESERVATIVEM F.D. & C. YELLOW COLOR #5 & #6 (TARTRAZINE) ARTIFICIAL COLORS) Primary Packaging: CHINA NOODLE CO. STEAM NOODLE NET WEIGHT 10 LBS
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·H-0548-2026·2026-03-18

    Vegetarian Chicken Flavor Ramen Express contains undeclared Yellow #5

    Palmetto Gourmet Foods Inc. is recalling Vegetarian Chicken Flavor Ramen Express because the product contains undeclared Yellow #5 food coloring, a major allergen for some consumers.

    Product
    VEGETARIAN CHICKEN FLAVOR RAMEN Express Net wt 3oz (85g) Ingredients: Enriched unbleached flour (wheat flour***) Palm oil***" Contains: Wheat, Soy. UPC 8 10037 81004 2 Produced by PALMETTO GOURMET FOODS, INC SALUDA, SC 29138
    Category
    Food
    Distribution
    32 states
  • HighFDA (Food)·H-0551-2026·2026-03-18

    Frozen Blueberry Crumble Pie Recalled for Listeria Risk

    Willamette Valley Pie Company is recalling Frozen Raw Bulk 9 inch Blueberry Crumble Pie due to potential contamination with listeria monocytogenes. The frozen pies were sold to grocery retailers' in-store bakeries in Illinois and Oregon.

    Product
    Frozen Raw Bulk 9 inch Blueberry Crumble Pie ES (4 pies/case). Net wt. 38oz. UPC 00022518893257. Handmade - Willamette Valley Pie Company LLC. 1651 Eska Way, Silverton, OR. Frozen raw pies were sold frozen in bulk packaging to grocery retailers' in-store bakeries. They are inte
    Category
    Food
    Distribution
    2 states
  • HighCPSC·26324·2026-03-12

    Playground Swing Set Seats Recalled for Fall Hazard Risk to Children

    LFTE USA recalls about 7,200 playground swing set seats with faulty rivets that can fail, causing children to fall. One minor injury has been reported; stop using recalled swings immediately and contact the manufacturer for free replacement.

    Product
    Playground Swing Set Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26321·2026-03-12

    LIVEHOM 11-Drawer Dressers Recalled for Tip-Over and Entrapment Hazards

    LIVEHOM 11-Drawer fabric dressers sold on Amazon are unstable without wall anchoring, creating tip-over and entrapment hazards for children. About 370 units recalled; no injuries reported.

    Product
    LIVEHOM 11-Drawer Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26319·2026-03-12

    Stoney Games Recalls Kluster Magnet Games Due to Ingestion Hazard

    Stoney Games recalls Kluster magnet chess games with loose magnets posing serious ingestion hazard to children. No injuries reported to date.

    Product
    Kluster Fun Tabletop Magnet Chess Games
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0396-2026·2026-03-11

    Capsules with Undeclared Prescription Drugs Marketed Without FDA Approval

    Mojo Max Fusion XXX capsules contain undeclared sildenafil and tadalafil, prescription drugs marketed without FDA approval. All lots (exp. 12/31/2027) distributed nationwide should not be used.

    Product
    Mojo Max Fusion XXX, 500 mg, one capsule per blister card, 20 count box, Distributed by: Max Nutrition Inc. UPC 6 78945 36675 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V897000·2026-03-11

    2022-2024 Jeep Grand Cherokee Side Air Bag Connector Defect Recall

    Certain 2022-2024 Jeep Grand Cherokee and 2021-2024 Grand Cherokee L vehicles have an improperly secured front seat side air bag connector that may prevent deployment. Chrysler has remedied all affected vehicles.

    Product
    JEEP — 2024 JEEP GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0397-2026·2026-03-11

    MR. 7 SUPER 700000 Capsules Recalled for Undeclared Pharmaceutical Ingredients

    MR. 7 SUPER 700000 capsules distributed to 4 U.S. customers contain undeclared sildenafil and tadalafil and were marketed without FDA approval. Consumers who have this product should discontinue use and consult a healthcare provider.

    Product
    MR. 7 SUPER 700000 capsules, 1 capsule blister card, Distributed by mR. 7
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Food)·H-0620-2026·2026-03-11

    Lobster and Crab Ravioli recalled for undeclared allergens

    Perfect Pasta, Incorporated is recalling Lobster & Crab Ravioli due to undeclared shrimp, crab, lobster, pollock, whiting, and soy. The product was distributed to consignees in Utah only.

    Product
    Lobster & Crab Ravioli. Keep Frozen. Contains: Wheat, Eggs, Milk, Crustaceans-Shellfish. Product is intended to be further cooked. Weight: 1-10 pound (4.5g). Use within 6 months. 801-541-9292-www.FunarosPerfectPasta.com. 1391 So. 300 West Slc, Ut 84115.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1469-2026·2026-03-11

    Impella RP cardiac support device sensor malfunction recall

    Abiomed is recalling 291 Impella RP cardiac support devices because the differential pressure sensor may malfunction, causing sensor values to drift. Devices were distributed worldwide.

    Product
    Impella RP with SmartAssist. Product Code: 0046-0035.
    Category
    Medical Device
    Distribution
    Distributed nationwide