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

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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

6201–6225 of 89510

  • HighFDA (Food)·H-0303-2025·2025-07-23

    YoCrunch Snickers and Twix yogurt packages may contain plastic pieces

    YoCrunch Lowfat Yogurt with Toppers two-product packages containing vanilla yogurt with Snickers and Twix pieces are being recalled because of foreign material in the form of plastic pieces.

    Product
    YoCrunch Lowfat Yogurt with Toppers. Two-product package. Contains 8-6oz (170g) cups of Vanilla Yogurt with Snickers pieces (cup UPC 46675-00112), and 8-6oz (170g) cups of Vanilla Yogurt with Twix bar pieces (cup UPC 46675-00113). Two-Pack UPC 46675-02614. Keep Refrigerat
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0304-2025·2025-07-23

    YoCrunch strawberry and raspberry granola yogurt may contain plastic pieces

    A YoCrunch Lowfat Yogurt with Toppers two-product package containing strawberry and raspberry yogurt with granola is being recalled because of foreign material in the form of plastic pieces.

    Product
    YoCrunch Lowfat Yogurt with Toppers Two-product package. Contains 8-6oz (170g) cups of Strawberry Yogurt with Granola pieces (Cup UPC 46675-00010), and 8-6oz (170g) cups of Raspberry Yogurt with Granola pieces (Cup UPC 46675-01401). Two- Pack, UPC 46675-01401. Keep Refrige
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0293-2025·2025-07-23

    Cool Watermelon bars recalled over potential Listeria monocytogenes contamination

    Cool Watermelon Bar frozen stick novelties are being recalled because of potential Listeria monocytogenes contamination. The action covers 110,292 cases across all affected products.

    Product
    Cool Watermelon Bar (86270), stick novelties 2.5 FL. Oz (74mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a master case. Keep Frozen.
    Category
    Food
    Distribution
    23 states
  • HighFDA (Food)·H-0291-2025·2025-07-23

    Savagely Sour blue raspberry bars recalled over potential Listeria contamination

    Savagely Sour BlueRasberry Bar frozen stick novelties are being recalled because of potential Listeria monocytogenes contamination. The action covers 110,292 cases across all affected products.

    Product
    Savagely Sour BlueRasberry Bar (86265), stick novelties 2.5 FL. Oz (74mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a master case. Keep Frozen.
    Category
    Food
    Distribution
    23 states
  • HighFDA (Food)·H-0288-2025·2025-07-23

    Orange Cream bars recalled over potential Listeria monocytogenes contamination

    Orange Cream Bar frozen stick novelties are being recalled because of potential Listeria monocytogenes contamination. The action covers 110,292 cases across all affected products.

    Product
    Orange Cream Bar (86010), stick novelties 2.5 FL. Oz (74mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a master case. Keep Frozen.
    Category
    Food
    Distribution
    23 states
  • HighFDA (Drugs)·D-0518-2025·2025-07-23

    Levothyroxine sodium 25 microgram tablets assayed below the approved specification

    Levothyroxine Sodium Tablets, USP 25 mcg from Accord Healthcare are being recalled because the product is subpotent, with an assay below the approved specification. 82,159 bottles affected.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2118-2025·2025-07-23

    NIO-A intraosseous device stabilizer may not release properly after insertion

    The NIO-A NIO Intraosseous Device Adult is being recalled because a manufacturing error means the built-in stabilizer may not be released properly after deployment and insertion. 7,056 US units affected.

    Product
    Brand Name: NIO-A Product Name: NIO Intraosseous Device Adult Model/Catalog Number: 105000603 Software Version: N/A Product Description: NIO devices are a spring-based, automatic intra-osseous access device supplied Sterile and single use. Indicated for Intra-osseous access t
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0521-2025·2025-07-23

    Levothyroxine sodium 100 microgram tablets assayed below the approved specification

    Levothyroxine Sodium Tablets, USP 100 mcg from Accord Healthcare are being recalled because the product is subpotent, with an assay below the approved specification. 9,739 bottles affected.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0297-2025·2025-07-23

    YoCrunch vanilla yogurt with Twix pieces may contain plastic pieces

    YoCrunch Low Fat Yogurt with Toppers, Vanilla with Twix bar pieces, is being recalled because of foreign material in the form of plastic pieces.

    Product
    YoCrunch Low Fat Yogurt with Toppers, Vanilla with Twix bar pieces, Packaged in the following size containers: 1. Single Serve Cup, 6 oz. (170g) UPC 46675-00113 2. Multipack containing 4-4 oz. cups UPC 46675-01327 Keep Refrigerated. Distributed by Danone US, LLC, White Plai
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0525-2025·2025-07-23

    Omeprazole capsule bottle contained a foreign divalproex sodium tablet

    Omeprazole Delayed-release Capsules USP 20 mg are being recalled because a foreign Divalproex Sodium Extended-Release 250 mg tablet was found in a bottle. 1,476 bottles affected.

    Product
    OMEPRAZOLE — OMEPRAZOLE (OMEPRAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2125-2025·2025-07-23

    EMPOWR 3D knee 10mm tibial inserts were packaged with wrong implant

    EMPOWR 3D Knee Tibial Insert E-PLUS units, catalog number 341-10-711, are being recalled because of a packaging discrepancy in which incorrect tibial inserts were packaged. 20 units affected.

    Product
    Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEETM INS, 11L 10MM, VE Model/Catalog Number: 341-10-711 Software Version: NA Product Description: Enovis" knee devices are intended for treatment of patients who are candidates for knee arthroplasty p
    Category
    Medical Device
    Distribution
    18 states
  • HighFDA (Drugs)·D-0519-2025·2025-07-23

    Levothyroxine sodium 25 microgram bottles of 1000 assayed below specification

    Levothyroxine Sodium Tablets, USP 25 mcg in 1000-count bottles from Accord Healthcare are being recalled because the product is subpotent. 2,352 bottles are affected.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0299-2025·2025-07-23

    YoCrunch strawberry granola yogurt cups may contain plastic foreign material

    YoCrunch Low Fat Yogurt with Toppers, Strawberry with Granola pieces in 6 oz single serve cups, is being recalled because of foreign material in the form of plastic pieces.

    Product
    YoCrunch Low Fat Yogurt with Toppers, Strawberry with Granola pieces, Single Serve Cup, 6 oz. (170g) UPC 46675-00010. Keep Refrigerated. Distributed by Danone US, LLC, White Plains, NY 10605
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2116-2025·2025-07-23

    SwabCap disinfecting caps may have an incomplete seal allowing alcohol evaporation

    SwabCap Disinfecting Caps for needlefree connectors are being recalled because an incomplete seal may let isopropyl alcohol evaporate, which may result in inadequate disinfection. 1,445,600 units affected.

    Product
    SwabCap Disinfecting Cap for Needlefree Connectors: SwabSleeve, REF: SCXT3-5-2000; SwabCap, 200-ct. Box, REF: SCXT3-2000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0279-2025·2025-07-23

    Wei-Chuan dried black fungus slices tested positive for Salmonella

    Wei-Chuan branded Black Fungus Slice in 2.5 oz bags is being recalled because the wood-ear mushroom tested positive for Salmonella. 100 cases are affected.

    Product
    Wei-Chuan branded Black Fungus Slice. Net weight: 2.5 oz UPC#: 072869231321
    Category
    Food
    Distribution
    11 states
  • HighFDA (Drugs)·D-0533-2025·2025-07-23

    Rizatriptan 5 mg tablets exceed the acceptable intake limit for nitrosamine

    Rizatriptan Benzoate Tablets USP 5 mg are being recalled after detection of N-nitroso-dimethyl-rizatriptan above the FDA recommended acceptable intake limit.

    Product
    RIZATRIPTAN BENZOATE — RIZATRIPTAN BENZOATE (RIZATRIPTAN BENZOATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0520-2025·2025-07-23

    Levothyroxine sodium 50 microgram tablets assayed below the approved specification

    Levothyroxine Sodium Tablets, USP 50 mcg from Accord Healthcare are being recalled because the product is subpotent, with an assay below the approved specification. 54,227 bottles affected.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2115-2025·2025-07-23

    Access Vitamin B12 reagent lot can give erroneously low or high results

    Access Vitamin B12 Reagent lot 439850 is being recalled after complaints of erroneous results, which may lead to a delayed or improper diagnosis or repeat testing. 10,000 units are affected.

    Product
    Access Vitamin B12 Reagent, Catalog Number 33000, Lot Number 439850
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·25V476000·2025-07-22

    Nova Bus steering can turn without driver input from missing valve

    Nova Bus is recalling certain 2020-2023 LFS transit buses because the electric power steering system may be missing a check valve, allowing hydraulic pressure to turn the steering wheel on its own.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V478000·2025-07-22

    Winnebago airbag wiring can be caught in the seat mechanism

    Winnebago is recalling certain 2024-2026 motorhomes because Supplemental Restraint System wires can be caught in the seat mechanism when the front seats are adjusted, damaging them.

    Product
    WINNEBAGO — WINNEBAGO REVEL, EKKO, NAVION, VIEW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·25393·2025-07-21

    Above-ground pools recalled after nine children drowned using strap footholds

    Above-ground pools 48 inches and taller with compression straps over the vertical support legs are being recalled because the strap can create a foothold. CPSC believes nine children have drowned.

    Product
    48-inch and taller above-ground pools with compression straps running on the outside and over the vertical support legs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V475000·2025-07-21

    Rosenbauer Fire Trucks Recalled for Odometer Software Error

    Rosenbauer America is recalling 2019-2024 fire trucks because a software error may cause the odometer to freeze, potentially delaying critical safety maintenance.

    Product
    ROSENBAUER — ROSENBAUER AVENGER, COMMANDER, WARRIOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25389·2025-07-17

    CasaClean handheld steamers can leak steam or spew hot boiling water

    CasaClean Handheld Steamers, model DF-958, are being recalled because they can leak steam or spew hot boiling water. Thirteen consumers have received burns. About 23,000 units are affected.

    Product
    CasaClean Handheld Steamers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25391·2025-07-17

    VIVI e-bike lithium-ion batteries can overheat, posing fire and burn hazards

    36-volt lithium-ion batteries supplied with certain VIVI e-bikes are being recalled because they can overheat. Fourteen overheating incidents including three fires have been reported. About 24,000 units affected.

    Product
    36-volt lithium-ion batteries used with VIVI E-bikes
    Category
    Consumer Product
    Distribution
    Distributed nationwide