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 the agency’s own highest classification or reported deaths or serious injuries, 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

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Minimum severity

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

16326–16350 of 114187

  • HighFDA (Devices)·Z-1759-2024·2024-05-15

    Randox Clinical Chemistry Calibration Serum Recalled for Measurement Bias

    Randox Laboratories has recalled Clinical Chemistry Calibration Serum (Cal2351/Cal10388) due to negative bias in inorganic phosphate measurements on RX Series instruments. The issue could affect the accuracy of clinical chemistry test results.

    Product
    Clinical Chemistry Calibration Serum (Catalog number Cal2351) that is 20x5ml lyophilized human based serum covering 38 commonly used clinical chemistry tests.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1228-2024·2024-05-15

    Ice Cream Strawberry Gelato Recalled for Undeclared Yellow #5 Allergen

    Belgian Yummies is recalling 53 units of 5-liter strawberry gelato distributed in Florida due to undeclared Yellow #5 (Tartrazine) allergen. Consumers with Yellow #5 sensitivity should not consume this product.

    Product
    Belgian Yummies Homemade Ice Cream Strawberry Gelato. Packaged in 5 Liter gray carapina liner.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1758-2024·2024-05-15

    Spinal Fusion Device Recall: Setscrew Insertion and Tightening Issues

    SPINEART's PERLA TL 25D spinal fusion screws are being recalled due to difficulties with setscrew insertion inside the screw head. The setscrew may not be properly tightened or may be positioned incorrectly, potentially affecting spinal stability.

    Product
    PERLA TL 25D SCREW REF: TLF-DS 45 25-S TLF-DS 45 30-S TLF-DS 45 35-S TLF-DS 45 40-S TLF-DS 45 45-S TLF-DS 55 30-S TLF-DS 55 35-S TLF-DS 55 40-S TLF-DS 55 45-S TLF-DS 65 35-S TLF-DS 65 40-S TLF-DS 65 45-S TLF-DS 65 50-S The PERLA¿ TL system is intended to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1227-2024·2024-05-15

    DB Yummers Island Marinade BBQ Sauce Recalled for Unapproved Processing

    Detty Family Barbeque LTD is recalling DB Yummers Island Marinade Barbeque Sauce because it was not manufactured using an FDA-approved thermal processing procedure, creating potential for pathogenic contamination.

    Product
    DB Yummers Island Marinade Barbeque Sauce packaged in 19.5 glass bottles, 12 bottles per case, UPC 7487200103.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1762-2024·2024-05-15

    Hemodialysis Vascular Access Kit Recalled for Loose Metal Shavings

    Angiodynamics DURAFLOW 2 hemodialysis kits may contain loosely affixed metal shavings that could enter the bloodstream. Metal fragments may require surgical removal if they embolize.

    Product
    DURAFLOW 2, 32CM STRAIGHT BASIC KIT PG-Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103012035
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Food)·F-1223-2024·2024-05-15

    Goya Red Kidney Beans Recalled for Swollen and Leaking Cans

    Tradewind Foods de Puerto Rico Inc. is recalling Goya Red Kidney Beans due to swollen and leaking cans discovered during an FDA inspection. The affected product was distributed in Puerto Rico and St. Croix.

    Product
    Goya Red Kidney Beans, Net Wt.15.5oz.(439g), metal (tin) cans, 24 cans/15.5 oz. per case
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1774-2024·2024-05-15

    Vascular access device recalls due to metal shaving contamination risk

    Angiodynamics is recalling the BioFlo DuraMax 15.5F Single Valve Sheath VascPak Kit due to possible loose metal shavings. Metal shavings could enter the bloodstream and require surgical removal.

    Product
    BioFlo DuraMax 15.5F 24cm Single Valve Sheath VascPak Kit- Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H965103038181
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Food)·F-1222-2024·2024-05-15

    Dietary Supplement Labeling Error: Kirkman 5-MTHF Folic Acid Misdeclared

    Kirkman 5-MTHF dietary supplement has a labeling error: the Supplement Facts incorrectly states 5000mcg Folic Acid per serving instead of 1000mcg. Lot# 477-0016, exp. 08/2025.

    Product
    Kirkman brand 5-MTHF Methyltetrahydrofolate 1mg capsule dietary supplement, Folate 1667mcg DFE, 5000mcg Folic Acid, 120 capsules per package, UPC 8 12325 02354 7. Manufactured exclusively by: Kirkman, Lake Oswego, OR 9703,
    Category
    Drug
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-1786-2024·2024-05-15

    Evidence MultiSTAT analyzer foam gasket malfunction may affect test accuracy

    Randox Laboratories is recalling 40 units of the Evidence MultiSTAT analyzer because a foam gasket defect may allow light to leak into the camera during testing, potentially affecting result accuracy and delaying reporting.

    Product
    Evidence MultiSTAT with software v 3.7-Analyzer intended for the qualitative determination of parent drug molecule and metabolites of drugs in human urine Catalog Number: EV4115
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0490-2024·2024-05-15

    Prescription skin cleanser recalled nationwide due to subpotency

    Acella Pharmaceuticals recalled 7,104 bottles of Sodium Sulfacetamide 10% Sulfur 5% Cleanser nationwide because the product contained less active ingredient than labeled. The recall was terminated in December 2025.

    Product
    SODIUM SULFACETAMIDE 10 SULFUR 5 CLEANSER — SODIUM SULFACETAMIDE 10 SULFUR 5 CLEANSER (SULFACETAMIDE SODIUM AND SULFUR)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1785-2024·2024-05-15

    Stryker Dynamic Mesh Mislabeled with Incorrect Catalog Number

    Stryker shipped 63 units of cranial mesh labeled as catalog 56-90614 (Gold) but actually containing 56-90314 (Blue) mesh. The mislabeling may cause procedural delays.

    Product
    Stryker 1,5/1,7MM DYNAMIC MESH- STD-MEDIUM-Intended for the reconstruction, stabilization and rigid fixation of the bony areas of the cranial skeleton. Catalog Number: 56-90614
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0492-2024·2024-05-15

    Clorazepate Dipotassium Tablets Recalled for Tablet Discoloration Defects Nationwide

    Aurobindo Pharma USA Inc. is recalling 6909 bottles of Clorazepate Dipotassium 7.5 mg tablets due to visible discoloration with yellow and dotted spots. No illnesses or injuries have been reported.

    Product
    CLORAZEPATE DIPOTASSIUM — CLORAZEPATE DIPOTASSIUM (CLORAZEPATE DIPOTASSIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0491-2024·2024-05-15

    Clorazepate Dipotassium Tablets Recalled Due to Cosmetic Discoloration

    Aurobindo Pharma USA Inc. is recalling Clorazepate Dipotassium Tablets 3.75 mg due to yellow dots and discoloration on some tablets distributed nationwide.

    Product
    CLORAZEPATE DIPOTASSIUM — CLORAZEPATE DIPOTASSIUM (CLORAZEPATE DIPOTASSIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V335000·2024-05-14

    2025 Freightliner Business Class M2 park brake failure recall

    Daimler Trucks North America is recalling 2024-2025 Freightliner Business Class M2 vehicles because the park brake valve module may leak, causing park brake failure or unexpected engagement while driving.

    Product
    FREIGHTLINER — FREIGHTLINER BUSINESS CLASS M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V336000·2024-05-14

    Thomas Built Buses Recalls 2024-2025 SAF-T-Liner C2 Models for Brake Defect

    Daimler Trucks North America is recalling 2024-2025 Thomas Built SAF-T-Liner C2 school buses because a seal defect may cause parking brake failure or unexpected engagement.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2 JOULEY, SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V338000·2024-05-14

    2024 Kia EV9 Front Passenger Seat Belt Retractor May Fail

    Kia is recalling certain 2024 EV9 vehicles because the front passenger seat belt retractor cover may not be properly secured, which can prevent the seat belt from locking correctly during a crash.

    Product
    KIA — KIA EV9
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V333000·2024-05-14

    Mack MD and Terrapro trucks recalled for incorrect weight rating

    Mack is recalling certain 2024-2025 MD and Terrapro vehicles because the Gross Axle Weight Rating (GAWR) on the certification label is incorrect, allowing vehicles to be overloaded and increasing crash risk. Dealers will replace the label free of charge.

    Product
    MACK — MACK TERRAPRO (TE), MD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V332000·2024-05-13

    ABC Bus Recalls Van Hool CX35 and CX45 Due to Heater Exhaust Risk

    ABC Bus is recalling 2023-2024 Van Hool CX35 and CX45 buses because Hydronic L-II heaters may release excessive exhaust gas, posing a risk of smoke poisoning or fire.

    Product
    VAN HOOL — VAN HOOL CX35, CX45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V334000·2024-05-13

    Winnebago Recalls 2020 Commercial Vehicle for Wheelchair Lift Defect

    Winnebago is recalling one 2020 Commercial vehicle because the wheelchair lift's outer barrier may deploy unexpectedly, increasing injury risk.

    Product
    WINNEBAGO — WINNEBAGO COMMERCIAL VEHICLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V330000·2024-05-10

    Lincoln Corsair transmission control software defect causes unexpected neutral shift

    Ford is recalling 2021-2022 Lincoln Corsair vehicles due to a hybrid powertrain control module software defect that may cause the transmission to shift into neutral unexpectedly, resulting in loss of drive power and increased crash risk.

    Product
    FORD — FORD, LINCOLN MAVERICK, ESCAPE, CORSAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V323000·2024-05-10

    Spartan Fire Recalls 2022-2024 Fire Apparatus Due to Seat Fastener Defect

    Spartan Fire is recalling 2022-2024 Gladiator, Metro Star, and FC-94 vehicles because undersized seat mount fasteners may break, increasing injury risk in a crash.

    Product
    SPARTAN FIRE — SPARTAN FIRE METROSTAR, GLADIATOR, FC-94
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V325000·2024-05-10

    Forest River Recalls 2024 Aurora Travel Trailers Due to Wiring Defect

    Forest River is recalling 2024 Aurora travel trailers because an incorrectly wired breakaway switch may fail to activate if the trailer detaches, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER AURORA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V331000·2024-05-10

    2022 Mercedes-Benz EQB Front Axle Drivetrain Rollaway Risk Recall

    Mercedes-Benz recalls 2022 EQB 300 and 350 vehicles due to improperly welded front axle gears that may fail, causing vehicle rollaway and crash risk. Dealers will replace the front axle drivetrain free of charge.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ EQB 300 4MATIC, EQB 350 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide