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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Minimum severity

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

Clear filters

4001–4025 of 6120

  • SevereFDA (Drugs)·D-0180-2023·2023-02-01

    Epinephrine API Recalled for Discoloration and Reduced Efficacy

    Spectrum Laboratory Products recalls Epinephrine (L-Adrenaline) USP in multiple lot sizes due to discoloration that could reduce the product's effectiveness. The recall affects shipments distributed nationwide in the USA, Puerto Rico, and Canada.

    Product
    Epinephrine (L-Adrenaline), USP, CAS 51-43-4, Packaged in amber glass bottles in a vacuum sealed pouch as (a)100 G; (b)1 G, (c) 25 G, (d) 5 G; Rx only. Repackaged by Spectrum Chemical Mfg. Corp. Gardena, CA 90248; New Brunswick, NJ 08901.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0960-2023·2023-02-01

    Getinge Flow-c Anesthesia System Software Bug May Prevent Ventilation

    The Getinge Flow-c Anesthesia System contains a software bug that can prevent pressure buildup and ventilation delivery. Under certain conditions, oxygen delivery may decrease, which may lead to hypoventilation and hypoxia.

    Product
    Getinge Flow-c Anesthesia System, Part No. 6887700
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0183-2023·2023-02-01

    Advil Liqui Gels Minis Recalled for Illegible Label Due to Adhesive Migration

    Glaxosmithkline Consumer Healthcare is recalling Advil Liqui Gels (minis) 200mg capsules nationwide due to illegible labeling caused by adhesive migration. Consumers should discard affected product or return it to the retailer.

    Product
    Advil Liqui Gels (minis), Solubilized ibuprofen capsules, 200mg, Pain Reliever Fever Reducer (NSAID), 200 liquid filled capsules, Pfizer, Madison, NJ 07940, UPC 3 0573 1769 13 5
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0181-2023·2023-02-01

    Advil Ibuprofen Tablets Recalled for Illegible Labels

    Glaxosmithkline Consumer Healthcare is recalling Advil ibuprofen 200 mg tablets because adhesive migrated onto labels, causing them to tear when peeled. This affects 321,246 tablets distributed nationwide.

    Product
    Advil (ibuprofen) Tablets, 200 mg, packaged as a) 360-count bottles (UPC 3 0573 0154 60 4), and b) 200-count bottles (UPC 3 0573 0154 21 5), Pfizer, Madison, NJ 07940
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0311-2023·2023-02-01

    Parsley from Mexico recalled due to Salmonella contamination

    FreshPoint South Florida, Inc. is recalling FC Parsley Curly Chopped Fine imported from Mexico due to Salmonella contamination. Approximately 1,269 cases were distributed in Florida.

    Product
    FC Parsley Curly Chopped Fine,12 Count, 2 1.5 Refrigerated at 34F, 301193, UPC 10022363, Parsley 12 CT, DIST BY FPSF, 22363 LOC 51, Parsley 6 CT, DIST BY FPSF, 22363 LOC 51
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-0959-2023·2023-02-01

    Getinge Flow-i Anesthesia Systems Recalled for Software Ventilation Defect

    Getinge Flow-i Anesthesia Systems models C20, C30, and C40 are being recalled due to a software bug that can prevent proper ventilation, potentially leading to hypoxia in patients.

    Product
    Getinge Flow-i Anesthesia Systems Flow-i C20, Part no. 6677200 Flow-i C30, Part no. 6677300 Flow-i C40, Part no. 6677400
    Category
    Medical Device
    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
  • 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 (Food)·F-0299-2023·2023-01-25

    Greco and Sons Frozen Dough Products Recalled for Undeclared Milk

    Sysco Merchandising and Supply is recalling multiple Greco and Sons frozen dough products because they contain undeclared milk allergen. Consumers with milk allergies should not consume these products.

    Product
    Greco and Sons Dough Room Product No. 15 FRZN DOUGH 6 oz.; Greco and Sons Dough Room Product No. 16 FRZN DOUGH 8 oz.; Greco and Sons Dough Room Product No. 18 FRZN DOUGH 10 oz.; Greco and Sons Dough Room Product No. 26 FRZN DOUGH 12 oz.; Greco and Sons Dough Room Product No. 19 F
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0297-2023·2023-01-25

    Greco and Sons dough products recalled for undeclared milk allergen

    Sysco Merchandising and Supply recalls Greco and Sons dough products containing undeclared milk allergen. Affected products were distributed to food service locations in six states.

    Product
    Greco and Sons Dough Room Product No. 92 House of 1000 10 oz.; Greco and Sons Dough Room Product No. 81 House of 1000 15 oz.; Greco and Sons Dough Room Product No. 37 Handlebar 27 oz.; Greco and Sons Dough Room Product No. 38 Handlebar 23 oz.; Greco and Sons Dough Room Product No
    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, 0998-UC-08
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V026000·2023-01-25

    2022-2023 BMW i4 and iX Vehicles Lack Pedestrian Warning Sounds

    BMW is recalling 2022-2023 i4 eDrive40 and iX xDrive50 electric vehicles because the external pedestrian warning sound system may fail during start-up. Pedestrians could be unaware of approaching vehicles, increasing injury risk.

    Product
    BMW — 2023 BMW I4
    Category
    Vehicle
    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 Produ
    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
  • SevereFDA (Food)·F-0290-2023·2023-01-25

    Alfalfa Sprouts Recalled Due to Potential Salmonella Contamination

    Sun Sprouts Alfalfa Sprouts packaged in 4 oz clamshells and 2.5 lb boxes have been recalled due to potential Salmonella contamination. The affected products were sold to distributors and retailers in Nebraska, Kansas, and Iowa.

    Product
    Sun Sprouts Alfalfa Sprouts packaged in 4 oz plastic clamshell, 6/4 oz or 12/4 oz containers per case; Sun Sprouts Alfalfa Sprouts packaged in 2.5lb plastic lined box.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0294-2023·2023-01-25

    Sysco Greco and Sons Dough Products Recalled for Undeclared Milk Allergen

    Sysco Merchandising and Supply is recalling Greco and Sons dough products sold in six states due to undeclared milk allergen. The recall affects approximately 2,325 cases with Best if Used By dates between December 1, 2022 and June 1, 2023.

    Product
    Greco and Sons Dough Room Product No. 28 Stefano 12 oz.; Greco and Sons Dough Room Product No. 29 Stefano 20 oz.; Greco and Sons Dough Room Product No. 30 Stefano 26 oz.; Greco and Sons Dough Room Product No. 36 Stefano 24 oz.; Greco and Sons Dough Room Product No. 35 Stefano 15
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0300-2023·2023-01-25

    Greco and Sons dough ball products recalled for undeclared milk allergen

    Sysco is recalling Greco and Sons dough ball products due to undeclared milk allergen. Consumers with milk allergies should not consume these products.

    Product
    Greco and Sons Dough Room Product No. 79 North Park Lounge 10 oz.; Greco and Sons Dough Room Product No. 64 North Park Lounge 16 oz.
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Devices)·Z-0926-2023·2023-01-25

    Medical device controller software update addresses critical failure

    Cardiac Assist is issuing a software update for LifeSPARC Controller units that may experience critical failure causing the system to freeze, crash, or lose display functionality. Affected units are identified by specific serial numbers.

    Product
    SHIP KIT, LIFESPARC, CONTROLLER AND ACCESSORIES - 5900-0000; SHIP KIT, LIFESPARC, CONTROLLER ONLY - 5900-0001. Component of LifeSPARC System, used to pump the blood through an extracorporeal circuit.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0298-2023·2023-01-25

    Sysco Greco and Sons Dough Products Recalled for Undeclared Milk Allergen

    Sysco is recalling Greco and Sons Dough Room products due to undeclared milk allergen. Affected products include 8 oz and 16 oz sizes distributed to six states.

    Product
    Greco and Sons Dough Room Product No. 61 Dad's 8 oz.; Greco and Sons Dough Room Product No. 62 Dad's 16 oz.
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0301-2023·2023-01-25

    Dough Ball Products Recalled for Undeclared Milk Allergen

    Sysco Merchandising and Supply is recalling Greco and Sons Dough Room pizza dough products due to undeclared milk allergen. Consumers with milk allergies should not consume these products.

    Product
    Greco and Sons Dough Room Product No. 12 Vic's Pizza 10 oz.; Greco and Sons Dough Room Product No. 17 Vic's Pizza 20 oz.
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Devices)·Z-0908-2023·2023-01-18

    Philips Fetal Spiral Electrode may break off during labor monitoring

    Philips is recalling fetal spiral electrodes used for labor monitoring because the spiral tip can break off during use, requiring surgery to remove the fragment from the newborn.

    Product
    Philips Fetal Spiral Electrode-intended for patients requiring fetal heart rate monitoring during labor. PN: 989803137631
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0882-2023·2023-01-18

    Philips Trilogy 100 Ventilator Foam May Separate and Block Air Inlet

    Silicone sound abatement foam in some Philips Trilogy 100 ventilators may separate and block the air inlet, potentially reducing delivered therapy volume or pressure and causing device alarms.

    Product
    Philips Trilogy 100 Ventilator, Model Numbers 1054260, 1054096, U1054260, U1054260B, 1054260B, CA1054096B, BT1054260, 1054096B, R1054260, RSL1054260, CA1054096, R1054260B, R1054655TPV, AU1054096, AU1054096B, 1054096B, 1054097, BR1054096, LA1054096, CN1054096, KO1054096, KR1054096
    Category
    Medical Device
    Distribution
    Distributed nationwide