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

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

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

25951–25975 of 114516

  • ModerateFDA (Devices)·Z-1019-2023·2023-02-01

    Air-Q3 intubating laryngeal airway size labeling discrepancy between IFU and device

    SunMed's Air-Q3 intubating laryngeal airway devices have a discrepancy between the Instructions For Use and the printed text on the device regarding orogastric tube sizes, which could cause confusion when placing gastric catheters.

    Product
    Air-Q3 AirQ3 Standard ILA with Manual Cuff Inflation and GA Size REF Number 0.0 50005 0.5 50055 1.0 50105 1.5 50155 2.0 50205 3.0 50305 4.0 50405
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0174-2023·2023-02-01

    Clobetasol Propionate Cream recalled due to subpotent drug

    Lupin Pharmaceuticals is recalling Clobetasol Propionate Cream 0.05% nationwide because stability testing revealed insufficient active ingredient in the affected lot.

    Product
    CLOBETASOL PROPIONATE — CLOBETASOL PROPIONATE (CLOBETASOL PROPIONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0172-2023·2023-02-01

    FDA Recalls Fentanyl Injection Solution for Underfilled Cassettes

    OurPharma LLC is recalling 768 cassettes of FentaNYL Citrate injection solution due to underfilled units. The affected product was distributed in Illinois and Missouri.

    Product
    FentaNYL Citrate 2.5mg/50mL (50mcg/mL) Injection Solution, Preservative-Free IV Injection 50mL Cassette, Rx Only, OurPharma, LLC, 2512 S. City Lake Rd., Fayetteville, AR 72701, NDC 73013-1001-01.
    Category
    Drug
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1016-2023·2023-02-01

    Intraoperative PTH Test Kits Recalled Due to High Result Variability

    Future Diagnostics recalled STAT-IntraOperative-Intact-PTH immunoassay kits due to high coefficient of variability in test results. 342 kits were distributed worldwide.

    Product
    Future Diagnostics STAT-IntraOperative-Intact-PTH (STAT-IO-I-PTH) Immunoassay kit REF 4K-IPT-00. in vitro diagnostic.
    Category
    Medical Device
    Distribution
    7 states
  • SevereUSDA FSIS·003-2023·2023-01-31

    Conagra Recalls Canned Meat and Poultry Due to Packaging Defect

    Conagra Brands is recalling approximately 2.6 million pounds of canned meat and poultry products due to a packaging defect that could allow contamination.

    Product
    ConAgra Brands, Inc. — Conagra Brands Recalls Canned Meat and Poultry Products Due to Possible Packaging Defect
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·23V038000·2023-01-31

    2022–2023 Hyundai Santa Cruz and Tucson roof moldings may detach

    Hyundai is recalling certain 2022 Santa Cruz and 2023 Santa Cruz vehicles, as well as 2022 Tucson vehicles, because the roof moldings may detach and become a road hazard.

    Product
    HYUNDAI — HYUNDAI SANTA CRUZ, TUCSON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·002-2023·2023-01-30

    Wild Cajun Meals Recalls Frozen Jambalaya and Gumbo for Lack of Inspection

    Wild Cajun Meals LLC is recalling approximately 18,418 pounds of frozen jambalaya and gumbo produced without federal inspection. The products were distributed in Louisiana and Texas.

    Product
    Wild Cajun Meals LLC Recalls Frozen, Fully Cooked Jambalaya and Gumbo Products Produced without Benefit of Inspection
    Category
    Food
    Distribution
    2 states
  • SevereUSDA FSIS·001-2023·2023-01-29

    Daniele International Recalls Ready-to-Eat Sausage Products Due to Listeria Risk

    Daniele International LLC is recalling approximately 69,255 pounds of ready-to-eat sausage products that may be contaminated with Listeria monocytogenes.

    Product
    Daniele Operating, LLC - Stedagio — Daniele International LLC Recalls Ready-to-Eat Sausage Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·23V035000·2023-01-29

    2023 Kia Telluride Side Air Bag Wire Harness Damage Recall

    Kia is recalling certain 2023 Telluride vehicles because manufacturing errors may have damaged the second row seat side air bag wire harnesses, preventing deployment in a crash.

    Product
    KIA — KIA TELLURIDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V034000·2023-01-27

    Bentley Recalls 2020 Continental GT Models Due to Fire Risk

    Bentley is recalling 2020 Continental GT and GTC vehicles because liquid entering the coolant pump may cause an electrical short circuit, increasing the risk of a vehicle fire.

    Product
    BENTLEY — BENTLEY CONTINENTAL GT, CONTINENTAL GT CABRIO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V033000·2023-01-27

    Porsche Panamera coolant pump electrical short circuit increases fire risk

    Porsche is recalling certain 2017-2021 Panamera models because humidity can enter the external coolant pump, causing an electrical short circuit that increases the risk of vehicle fire. Dealers will replace the pump and inspect connections at no cost.

    Product
    PORSCHE — PORSCHE PANAMERA 4S, PANAMERA TURBO, PANAMERA TURBO EXECUTIVE, PANAMERA 4S SPORT TURISMO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·23V032000·2023-01-27

    2023 Winnebago Revel: incorrect tire size on safety label

    Certain 2023 Winnebago Revel camper vans have an incorrect tire size listed on the Tire and Loading Information Label (R16 instead of R17). Installing the wrong tires based on this incorrect information could increase the risk of a crash.

    Product
    WINNEBAGO — WINNEBAGO REVEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23107·2023-01-26

    ZLINE Gas Ranges Recalled Due to Carbon Monoxide Emission Hazard

    ZLINE is recalling about 30,000 gas ranges (30-inch, 36-inch, and 48-inch models) because the oven compartment can emit dangerous levels of carbon monoxide, posing a serious risk of injury or death. Consumers should stop using the oven immediately until repaired.

    Product
    ZLINE 30-inch, 36-inch and 48-inch RG gas ranges
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V030000·2023-01-26

    Jaguar I-PACE vehicles recalled for insufficient pedestrian warning sounds

    Jaguar is recalling 2021-2022 I-PACE vehicles because they fail to produce sufficient pedestrian warning sounds when stationary or in reverse, violating federal safety standards. Dealers will update the audio amplifier software at no charge.

    Product
    JAGUAR — JAGUAR I-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V031000·2023-01-26

    Land Rover Range Rover Sport PHEV Pedestrian Warning Sound Defect

    Land Rover is recalling certain 2020-2022 Range Rover PHEV and Range Rover Sport PHEV vehicles because they fail to make sufficient warning sounds when stationary and in reverse, violating federal safety standards for hybrid and electric vehicles.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER SPORT PHEV, RANGE ROVER PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23106·2023-01-26

    Children's Lounge Pants Recalled for Flammability Standards Violation

    Properly Tied is recalling about 1,960 children's lounge pants that fail to meet federal flammability standards for sleepwear, posing a burn injury risk to children. Consumers should stop using them immediately and contact Properly Tied for return instructions.

    Product
    Children's Lounge Pants
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0886-2023·2023-01-25

    Cardiosave IABP may shut down unexpectedly due to blood contamination

    The Cardiosave Rescue Intra-Aortic Balloon Pump may shut down unexpectedly if blood enters the device through a compromised balloon catheter. Approximately 46 units have been distributed worldwide.

    Product
    Cardiosave Rescue Intra-Aortic Balloon Pump (IABP), Model Numbers 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85, 0998-UC-0800-75, 0998-UC-0800-83, 0998-UC-0800-85.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0296-2023·2023-01-25

    Dough Ball Products Recalled for Undeclared Milk Allergen

    Sysco Merchandising and Supply is recalling Greco and Sons Dough Room dough ball products because they contain undeclared milk allergen, which poses a serious risk to milk-allergic consumers.

    Product
    Greco and Sons Dough Room Product No. 9009 Teresa's 9 oz.; Greco and Sons Dough Room Product No. 9012 Teresa's 12 oz.; Greco and Sons Dough Room Product No. 9020 Teresa's 22 oz.; Greco and Sons Dough Room Product No. 9046 Teresa's 48 oz.
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Devices)·Z-0885-2023·2023-01-25

    Cardiosave Hybrid Intra-Aortic Balloon Pump may shut down unexpectedly

    The Cardiosave Hybrid Intra-Aortic Balloon Pump may shut down unexpectedly when blood enters the device through a compromised balloon catheter during use.

    Product
    Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), Model Numbers 0998-00-0800-31, 0998-00-0800-32, 0998-00-0800-33, 0998-00-0800-34, 0998-00-0800-35, 0998-00-0800-36, 0998-00-0800-45, 0998-00-0800-52, 0998-00-0800-53, 0998-00-0800-55, 0998-00-0800-65, 0998-UC-0800-31…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0295-2023·2023-01-25

    Greco and Sons Dough Room Garlic Knots recalled for undeclared milk allergen

    Sysco Merchandising and Supply is recalling Greco and Sons Dough Room Garlic Knots due to undeclared milk allergen. Affected cases were distributed across six states with best-if-used-by dates between December 1, 2022, and June 1, 2023.

    Product
    Greco and Sons Dough Room Product No. 65 Garlic Knots 180/CS
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0293-2023·2023-01-25

    Greco and Sons Dough Room Products Recalled for Undeclared Milk Allergen

    Sysco Merchandising and Supply is recalling multiple Greco and Sons Dough Room products distributed in six states due to undeclared milk allergen. Consumers with milk allergies should not consume these products.

    Product
    Greco and Sons Dough Room Product No. 333 PUB DOUGH 9 oz.; Greco and Sons Dough Room Product No. 88 Christopher's 14 oz.; Greco and Sons Dough Room Product No. 84 Christopher's 20 oz.; Greco and Sons Dough Room Product No. 86 Christopher's 36 oz.; Greco and Sons Dough Room…
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0131-2023·2023-01-25

    Daptomycin for Injection Recalled Due to Incorrect Labeling Dosage

    Accord Healthcare is recalling Daptomycin for Injection labeled as 350 mg/vial but containing 500 mg/vial vials. The labeling error poses a dosing risk to patients.

    Product
    Daptomycin for Injection 350 mg/vial 1 Single-dose vial, Rx only, Manufactured for: Accord Healthcare, Inc., Durham, NC 27703 Manufactured by: Intas Pharmaceuticals Limited, Pharmez, Ahmedabad-382 213, India. NDC 16729-0434-05
    Category
    Drug
    Distribution
    Distributed nationwide