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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7376–7400 of 36565

  • SevereFDA (Food)·F-1592-2022·2022-08-24

    Vermont creamery recalls ice cream base mix due to Listeria contamination

    Kingdom Creamery of Vermont is recalling 14% Base Mix and Archie Case Mix ice cream base products due to Listeria monocytogenes contamination. A Class I FDA recall affects 1,623 cases distributed to Vermont, Maine, and Massachusetts.

    Product
    14% Base Mix Case:14% Archie Case Mix
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1597-2022·2022-08-24

    Rococo Ice Cream Base Mix Recalled Due to Listeria Contamination Risk

    Kingdom Creamery of Vermont LLC is recalling Rococo Ice Cream 15% base mix due to potential Listeria monocytogenes contamination. The recalled product was distributed in Vermont, Maine, and Massachusetts.

    Product
    Rococo Ice Cream 15% base mix; list Kingdom Creamery of Vermont on the product label
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1587-2022·2022-08-24

    Maple Soft Serve Mix Recalled Due to Potential Listeria Contamination

    Kingdom Creamery of Vermont is recalling its 5% Maple Soft Serve Mix due to potential Listeria monocytogenes contamination. The affected product was distributed in Vermont, Maine, and Massachusetts.

    Product
    Kingdom Creamery of Vermont 5% Maple Soft Serve Mix
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1591-2022·2022-08-24

    Kingdom Creamery Vermont Chocolate Soft Serve Mix Recalled for Listeria

    Kingdom Creamery of Vermont 10% Chocolate Soft Serve Mix is being recalled due to potential Listeria monocytogenes contamination. The product was distributed in Vermont, Maine, and Massachusetts.

    Product
    Kingdom Creamery of Vermont 10% Chocolate Soft Serve Mix
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1589-2022·2022-08-24

    Kingdom Creamery of Vermont Maple Soft Serve Mix Recalled for Listeria

    Kingdom Creamery of Vermont's 10% Maple Soft Serve Mix is being recalled due to potential Listeria monocytogenes contamination. The affected product was distributed in Vermont, Maine, and Massachusetts.

    Product
    Kingdom Creamery of Vermont 10% Maple Soft Serve Mix
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1558-2022·2022-08-24

    Albertsons Ready Meals Crab & Shrimp recalled for undeclared allergens

    Albertsons ready-to-eat meals may contain undeclared fish, shellfish, egg, wheat, and soy allergens. Consumers with allergies should not consume and should return the product.

    Product
    Ready Meals Crab & Shrimp w/Ccktl SCE NET WT 12 OZ CAL 310 NET WT. 0lb 12oz (340g) ready2eat UPC 23253500000 Store Banners: ACME, Albertsons, Andronico s Community Markets, Balducci s, Carrs-Safeway, Eagle, Jewel-Osco, King s, Pak N Save, Safeway, Shaw s, Star Market, Vons
    Category
    Food
    Distribution
    25 states
  • SevereFDA (Devices)·Z-1512-2022·2022-08-24

    HeartWare HVAD System Batteries Recalled for Critical Electrical Faults

    HeartWare HVAD System Batteries are being recalled due to electrical faults that may prevent the battery from powering the device controller, accepting charges, or maintaining charge. Approximately 19,616 batteries distributed worldwide are affected.

    Product
    HeartWare Ventricular Assist Device (HVAD) System Batteries, Product Number 1650DE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1556-2022·2022-08-24

    Albertsons Ready Meals Shrimp recalled for undeclared fish and shellfish allergens

    Albertsons Companies recalled Ready Meals Shrimp Cooked with Cocktail Sauce for undeclared fish and shellfish allergens. The product was distributed across 24 US states.

    Product
    Ready Meals Shrimp Cooked with Cocktail Sauce SCE NET WT 12 OZ CAL 330 NET WT. 0lb 12oz (340g) ready2eat Tomato paste, water, high fructose corn syrup, distilled vinegar, horseradish, salt, lemon juice concentrate, soybean oil, beet powder, natural and artificial flavor, zanthan
    Category
    Food
    Distribution
    25 states
  • SevereFDA (Food)·F-1586-2022·2022-08-24

    FDA Recalls Kingdom Creamery Vanilla Soft Serve Mix for Listeria Risk

    Kingdom Creamery of Vermont is recalling 5% Vanilla Soft Serve Mix due to potential Listeria monocytogenes contamination. The affected product was distributed in Vermont, Maine, and Massachusetts.

    Product
    Kingdom Creamery of Vermont 5% Vanilla Soft Serve Mix
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1555-2022·2022-08-24

    Marutomo Dashi Soup Base Recalled Due to Undeclared Wheat and Soy Allergens

    Wismettac Asian Foods recalls Marutomo Dashi Soup Base due to undeclared wheat and soy allergens. The product may pose serious allergic reaction risk to sensitive consumers.

    Product
    Marutomo Dashi Soup Base, Item # #37402 Ingredients: Dried Shaved Skipjack Tuna, Fish Extract (Dried Skipjack Tuna, Salt, Sea Bream Bone, Yeast Extract), Kelp Extract (Kelp Extract, Sorbitol, Maltitol, Hydrogenated Starch Hydrolysate (Cassava), Salt, Ethyl Alcohol, Kelp Product
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-1599-2022·2022-08-24

    Ice cream base mix recalled due to listeria monocytogenes contamination

    SOCO Creamery ice cream base mix is being recalled due to potential Listeria monocytogenes contamination. Affected consumers in Vermont, Maine, and Massachusetts should discard the product.

    Product
    SOCO Creamery 15% Base Mix; the label also lists Kingdom Creamery of Vermont
    Category
    Food
    Distribution
    3 states
  • SevereNHTSA·22V634000·2022-08-19

    Thomas Built Buses Recalls Saf-T-Liner HDX School Buses for Seat Barrier Defect

    Daimler Trucks North America is recalling 2011-2021 Thomas Built Saf-T-Liner HDX school buses because forward seat barriers may not provide sufficient protection, increasing injury risk in crashes.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1399-2022·2022-08-17

    FDA Recalls 3.95 Million Viral Transport Containers Distributed Without Clearance

    The FDA recalled 3.95 million viral transport containers distributed without FDA clearance and in violation of established guidance. The containers were distributed worldwide, including to facilities in California, Florida, Illinois, and New York.

    Product
    HXBL/WETEX/Genesis Biomedical Viral Transport Container, Model No. HX-K59-1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1485-2022·2022-08-17

    Cobalt Implantable Cardioverter Defibrillators recalled for reduced shock energy

    Medtronic's Cobalt implantable cardioverter defibrillators may deliver approximately 79% of programmed shock energy during high-voltage therapy. Patients with affected models should contact their physician.

    Product
    Cobalt Implantable Cardioverter Defibrillators: a. Cobalt XT VR ICD, Model Numbers: DVPA2D1, DVPA2D4; b. Cobalt XT DR ICD, Model Numbers: DDPA2D1, DDPA2D4
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1400-2022·2022-08-17

    Viral Transport Container Distributed Without FDA Clearance or Guidance Compliance

    Haimen Shengbang Laboratory Equipment recalled 100,000 viral transport containers distributed without FDA clearance and outside FDA guidance, affecting facilities in California, Florida, Illinois, New York, and China.

    Product
    HXBL/WETEX/Genesis Biomedical Viral Transport Container, Custom Made
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1488-2022·2022-08-17

    Cobalt Implantable Defibrillators May Deliver Reduced Shock Energy

    Medtronic Cobalt implantable cardioverter defibrillators may deliver approximately 79% of programmed shock energy during high-voltage therapy. The reduced energy could affect device performance in patients requiring defibrillation.

    Product
    Cobalt Implantable Cardioverter Defibrillators with Cardiac Resynchronization Therapy (CRT-D): a. Cobalt HF CRT-D, Model Numbers: DTPB2D4, DTPB2D1; b. Cobalt HF Quad CRT-D, Model Numbers: DTPB2QQ, DTPB2Q1
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1487-2022·2022-08-17

    Cobalt Implantable Cardioverter Defibrillators May Deliver Reduced Shock Energy

    Certain Cobalt implantable cardioverter defibrillators may deliver approximately 79% of programmed shock energy during therapy, potentially reducing treatment effectiveness. Medtronic is recalling affected units worldwide.

    Product
    Cobalt Implantable Cardioverter Defibrillators: a. Cobalt VR ICD, Model Numbers: DVPB3D1, DVPB3D4; b. Cobalt DR ICD, Model Numbers: DDPB3D1, DDPB3D4
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1398-2022·2022-08-17

    FDA Recalls Viral Transport Containers Distributed Without Clearance

    FDA recalls approximately 8.7 million viral transport containers that were distributed without regulatory clearance and without complying with FDA guidance for proper viral transport specifications.

    Product
    HXBL/WETEX/Genesis Biomedical Viral Transport Container, Model No. HX-K59 Activated Type
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1489-2022·2022-08-17

    Crome Implantable Cardioverter Defibrillators Recalled for Reduced Shock Energy

    Medtronic is recalling 1,657 Crome implantable cardioverter defibrillators due to potential reduced shock energy during high-voltage therapy. Affected devices may deliver only 79% of programmed energy.

    Product
    Crome Implantable Cardioverter Defibrillators: a. Crome VR ICD, Model Numbers: DVPC3D1, DVPC3D4; b. Crome DR ICD, Model Numbers: DDPC3D1, DDPC3D4
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1486-2022·2022-08-17

    Medtronic Cobalt Implantable Defibrillators Recalled Due to Reduced Shock Energy Defect

    Medtronic has recalled 8,429 Cobalt implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) worldwide due to potential reduced shock energy during therapy, potentially delivering 79% of programmed energy.

    Product
    Cobalt Implantable Cardioverter Defibrillators with Cardiac Resynchronization Therapy (CRT-D): a. Cobalt XT HF CRT-D, Model Numbers: DTPA2D4, DTPA2D1; b. Cobalt XT HF Quad CRT-D, Model Numbers: DTPA2QQ, DTPA2Q1
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1490-2022·2022-08-17

    Crome Implantable Cardioverter Defibrillators may deliver reduced shock energy

    Medtronic recalls 866 Crome implantable defibrillators due to potential reduced shock energy delivery during high-voltage therapy, affecting devices worldwide. Patients should contact their physician to determine if their device is affected.

    Product
    Crome Implantable Cardioverter Defibrillators with Cardiac Resynchronization Therapy (CRT-D): a. Crome HF CRT-D, Model Numbers: DTPC2D4, DTPC2D1; b. Crome HF Quad CRT-D, Model Numbers: DTPC2QQ, DTPC2Q1
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-1542-2022·2022-08-17

    Big Olaf frozen ice cream recalled for potential Listeria monocytogenes contamination

    Big Olaf frozen ice cream products in all flavors and sizes distributed in Florida and Ohio are being recalled due to potential Listeria monocytogenes contamination. Listeria can cause serious illness.

    Product
    Big Olaf, Frozen Ice Cream to include all flavors, sold in sizes 2.5 gal, 1/2 gal, and pints packaged in plastic containers.
    Category
    Food
    Distribution
    2 states
  • SevereNHTSA·22E069000·2022-08-17

    S&B Diesel Fuel Tank Recall for Insufficient Driveline Clearance

    S&B Filters is recalling certain diesel fuel tanks for RAM Mega Cab vehicles due to insufficient clearance that may cause fuel leaks and fire risk.

    Product
    FUEL SYSTEM, DIESEL:STORAGE:TANK ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·22200·2022-08-15

    4moms MamaRoo and RockaRoo Baby Swings and Rockers Strangulation Hazard

    4moms is recalling over 2 million MamaRoo baby swings and 220,000 RockaRoo rockers because dangling restraint straps pose a strangulation hazard to crawling infants. One death has been reported.

    Product
    4moms MamaRoo Baby Swing, versions 1.0 through 4.0 and RockaRoo Baby Rockers
    Category
    Consumer Product
    Distribution
    Distributed nationwide