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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18826–18850 of 114351

  • SevereFDA (Devices)·Z-0592-2024·2024-01-10

    Tracheostomy care kits recalled for sterility assurance failure

    Busse Hospital Disposables is recalling tracheostomy care kits containing Nurse Assist Sterile Normal Saline because the required sterility assurance level cannot be guaranteed. Contaminated products could cause serious infections including bloodstream, respiratory, and urinary tract infections, or sepsis.

    Product
    Catalog No. 800 TRACHEOSTOMY CARE TRAY - STERILE -LATEX FREE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0690-2024·2024-01-10

    Soy Bean Sprouts Recalled Due to Listeria Contamination

    Samsung Bean Sprout is recalling Sung Soy Bean Sprouts (1lb packages) distributed to Virginia due to Listeria monocytogenes contamination. Products have a sell-by date of 12/14/23.

    Product
    Sung Soy Bean Sprouts, 1lb packages, in plastic packages, 20 bags per case
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-0591-2024·2024-01-10

    Omnipod 5 insulin pump app bolus calculator decimal point error

    The Omnipod 5 app bolus calculator may fail to record a decimal point if entered first when adjusting a dose, potentially causing insulin over-delivery. Users should verify dose values on both the calculator and confirmation screens before administering insulin.

    Product
    Omnipod 5 App (on compatible Android smartphones), Software Versions 1.1 - 1.2.3 (current). US: PT-000599- Omnipod 5 App Software Package (provided through Google Play), EU: PT-001323- Omnipod 5 App Software Package (provided on locked-down Controllers (PT-001194 and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V013000·2024-01-10

    Western Star 4900 and 6900 Trucks Recalled for Parking Brake Defect

    Daimler Trucks North America is recalling 2023 Western Star 4900 and 6900 trucks because a parking brake defect may allow the vehicle to move unintentionally.

    Product
    WESTERN STAR — WESTERN STAR 6900, 4900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0593-2024·2024-01-10

    Dressing change tray recalled for sterility assurance failure

    Busse Hospital Disposables recalls sterile dressing change trays due to inability to guarantee required sterility assurance level. The defect could lead to serious infections including blood stream, urinary tract, or respiratory infections.

    Product
    Catalog No. 1443 DRESSING CHANGE TRAY / STERILE - LATEX FREE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0638-2024·2024-01-10

    Philips Trilogy Evo respiratory devices recalled for missing contraindication statement

    Philips recalled Trilogy Evo respiratory devices for missing contraindications in labeling. Devices lack warnings against use in pediatric patients under 10 kg and certain therapy modes, risking barotrauma and respiratory complications.

    Product
    Trilogy Evo and Trilogy Evo O2 Material Numbers BL2110X15B BR2110X18B CA2110X12B DE2100X13B DE2110X13B DS2100X11B DS2110X11B EE2100X15B EE2110X15B ES2100X15B ES2110X15B EU2100X15B EU2100X19 EU2110X15B FR2100X14B FR2110X14B FX2100X15B GB2110X15B IA2100X15B…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0627-2024·2024-01-10

    Merit Maestro Microcatheter Sterility Recall, 717 Units Distributed Worldwide

    Merit Medical Systems is recalling 717 units of Merit Maestro Microcatheters because their sterility cannot be guaranteed. Non-sterile devices could introduce infection when used in medical procedures.

    Product
    Merit Maestro Microcatheter, Reference Numbers: 28MC2111045/B, 28MC21110ST/B, 28MC2113045/B, 28MC21130SN/CNB, 28MC21130ST/B, 28MC2115045/B, 28MC2115045/C, 28MC21150SN/B, 28MC21150ST/B, 28MC2411045/D, 28MC24110SN/D, 28MC24110ST/D, 28MC2413045/D, 28MC24130SN/F…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0664-2024·2024-01-10

    Dietary supplement recalled due to potential mold contamination

    Spring Valley Biotin & Collagen Liquid is being recalled due to potential mold contamination. Approximately 24,324 units were distributed nationwide; consumers should stop using affected products.

    Product
    Spring Valley Biotin & Collagen Liquid, Natural Berry Flavor, 15000 mcg, Dietary Supplement 29 doses 1 fl oz (29mL) UPC: 194346065158 Packaged in a glass bottle in a paper carton
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0632-2024·2024-01-10

    Surgical Knife Crescent Recall Due to Incorrect Blade Angle

    Beaver Visitec International is recalling one lot of surgical knives where the blade is oriented incorrectly—bevel down instead of the required 55-degree bevel up. This defect could compromise surgical precision during use.

    Product
    Conventional Knife Crescent 2.5mm, 55 degrees bevel up, Part Number 373807
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0635-2024·2024-01-10

    EDS 3 CSF External Drainage System recalled for incomplete sterility testing

    Natus Medical is recalling 3,336 units of the EDS 3 CSF External Drainage System nationwide because incomplete bioburden testing cannot guarantee sterility. No illnesses have been reported, but non-sterile devices pose infection risk.

    Product
    EDS 3 CSF External Drainage System, REF: NT821731C, STERILEEO, Rx only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0633-2024·2024-01-10

    Xstar Kojo slit knife recalled for incorrect blade orientation

    One lot of Xstar Kojo Safety Slit Knife contains inverted blades (bevel down instead of bevel up). The 2160 affected units from lot 6049877 were distributed internationally, including to Japan.

    Product
    Xstar Kojo Safety Slit Knife, 2.5mm 45¿ Bevel Up, Part Number 373025
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0628-2024·2024-01-10

    FDA Recalls Merit Pursue Microcatheter Due to Sterility Concerns

    Merit Medical Systems is recalling Merit Pursue Microcatheter devices distributed worldwide because sterility cannot be guaranteed. Patients should contact their healthcare provider.

    Product
    Merit Pursue Microcatheter, REF: 28HC17130SN, 28HC17150ST/A, 29HC2015045/A, 29HC20150SN/A, 29HC20150ST, CE 2797, STERILEEO, Rx ONLY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0663-2024·2024-01-10

    Bobo's Oat Bars Recalled for Undeclared Coconut Allergen

    Bobo's Oat Bars - Peach are recalled due to undeclared coconut. The recall affects approximately 10,800 units sold under Lot Code 3J27111.

    Product
    Bobo's Oat Bars - Peach 3oz packaged in ALOX coated PET film, corrugate cartons and master case. 12 units per carton
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0631-2024·2024-01-10

    Covidien Valleylab FT10 Energy Platform software issue causes inoperability

    Covidien is recalling Valleylab FT10 FT Series Energy Platform devices due to a software issue that may render new systems inoperable. The recall affects 47,901 units distributed worldwide.

    Product
    Covidien Valleylab FT10, FT Series Energy Platform, REF: VLFT10GEN, DLVLFT10GEN, VLFT10GENZD
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V011000·2024-01-10

    2022-2023 Lucid Air defrost heater failure reduces windshield visibility

    Lucid is recalling 2022-2023 Air vehicles whose high voltage coolant heater may fail to defrost the windshield, reducing visibility and increasing crash risk. Lucid will provide a software update and replace failed heaters at no cost.

    Product
    LUCID — LUCID AIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0218-2024·2024-01-10

    Peritoneal Dialysis Solution Recalled for Lack of Sterility Assurance

    Fresenius Medical Care is recalling 69,590 bags of DELFLEX Peritoneal Dialysis Solution due to lack of sterility assurance. The affected lot was distributed nationwide.

    Product
    DELFLEX — DELFLEX (DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·24V010000·2024-01-10

    2024 Volvo XC40 Left Rear Turn Signal May Not Function

    Certain 2024 Volvo XC40 vehicles may have a software error in the Central Electronic Module that disables the left rear turn signal indicator, increasing the risk of a crash if other drivers are not notified of turning.

    Product
    VOLVO — VOLVO XC40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0711-2024·2024-01-10

    Racine Danish Kringles Raspberry Kringle Recalled for Undeclared Tree Nuts

    Racine Danish Kringles Raspberry Kringle (14 oz., lot 23299) is being recalled due to undeclared tree nuts (pecans). Consumers with nut allergies should not consume this product.

    Product
    Racine Danish Kringles Raspberry Kringle, 14 oz. UPC 0 45251-00312 7. RDK Corp, Racine, WI 53404.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0691-2024·2024-01-10

    Marinated Baby Milkfish Recalled for Botulism Risk Due to Missing Storage Instructions

    Foremost Foods is recalling Pamana Premium Marinated Baby Bangus due to potential botulism risk. The frozen product in reduced-oxygen packaging lacks required freezing and thawing instructions.

    Product
    Pamana Premium Marinated Baby Bangus (Deboned Marinated Baby Milkfish), Net Weight to be Weight at Time of Sale
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0639-2024·2024-01-10

    Spinal fixation screws recalled due to incorrect size laser marking

    Zimmer Biomet Spine Inc. is recalling Vitality Polyaxial Screws (7.5mm x 50mm) due to incorrect laser marking showing 7.5 x 40. Incorrect screw size could cause perforation and vascular damage during spinal surgery.

    Product
    Vitality Polyaxial Screw, 7.5mmx 50mm, REF: 07.02000.118, used with Vitality and Vital Spinal Fixation System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0623-2024·2024-01-10

    Medtronic Protege GPS Stent System Recalled for Packaging Seal Defects

    Medtronic is recalling Protege GPS Self-Expanding Peripheral Stent Systems due to seal defects in product packaging that could compromise sterility. Affected lot B644679 had national distribution.

    Product
    Protege GPS Self-Expanding Peripheral Stent System, product number SERB65-09-60-80, Sterile.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0629-2024·2024-01-10

    Microcatheter and Infusion Systems Recalled Due to Sterility Concerns

    Merit Medical Systems is recalling specific lots of microcatheter and infusion system devices because their sterility cannot be guaranteed. The devices were distributed worldwide including multiple US states and international locations.

    Product
    Fountain, REF: IS4-135-30 and IS4-90-10, CE2797, STERILEEO, Rx ONLY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0693-2024·2024-01-10

    Frozen Milkfish Recall Due to Missing Storage and Thawing Instructions

    Foremost Foods International is recalling Pamana Premium Bangus Belly frozen milkfish because the reduced-oxygen packaging lacks instructions to keep the product frozen and to thaw it properly, risking Clostridium botulinum toxin formation.

    Product
    Pamana Premium Bangus Belly (Cut Deboned Milkfish Belly), 340 g (120 oz)
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0689-2024·2024-01-10

    Seafood Medley Recalled for Potential Plastic Foreign Object

    Wegmans Seafood Medley (1 lb packages, Lot 47117) is being recalled because it may contain plastic foreign objects. The recall affects products distributed in Massachusetts, Pennsylvania, and New York.

    Product
    Wegmans Seafood Medley, 1lb.
    Category
    Food
    Distribution
    3 states