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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11326–11350 of 27718

  • SevereFDA (Food)·F-1654-2024·2024-08-14

    Al'Fez Natural Tahini Recalled for Potential Salmonella Contamination

    Al'Fez Natural Tahini in 5.6oz glass jars is being recalled due to potential Salmonella contamination. The recall affects 3,522 cases distributed nationwide.

    Product
    Al'Fez Natural Tahini in 5.6oz glass jars, UPC 711464506778
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2419-2024·2024-08-14

    CADD-Solis Ambulatory Infusion Pumps with Software Defects Affecting Device Responsiveness

    CADD-Solis Model 2100 infusion pumps with pre-v4.3 software have defects affecting occlusion detection and device responsiveness. Manufacturer recommends updating to software version 4.3 (2023) to resolve the issues.

    Product
    CADD-Solis Ambulatory Infusion Pumps, Model 2100. Intended for the following uses: Indicated for the following uses: Intra-arterial, subcutaneous, intraperitoneal, in close proximity to nerves, into an intraoperative site, epidural space or subarachnoid space. Therapies that re
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2443-2024·2024-08-14

    Medline Procedure Kits Recalled Due to Defective Plastic Syringes

    Medline procedure kits containing defective plastic syringes are being recalled nationwide. The syringes may leak, break, or have other quality issues that could pose a risk to patient health.

    Product
    Medline procedure kits labeled as: 1) NEPHROLOGY PACK, Pack Number DYNJ59089; 2) NERVE BLOCK TRAY, Pack Number DYNJRA1221A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2420-2024·2024-08-14

    CADD-Solis VIP Ambulatory Infusion Pump Class I Recall

    Smiths Medical is recalling CADD-Solis VIP Model 2110 infusion pumps in a Class I action affecting units worldwide.

    Product
    CADD-Solis VIP ambulatory Infusion Pumps, Model 2110. Indicated for the following uses: Intra-arterial, subcutaneous, intraperitoneal, in close proximity to nerves, into an intraoperative site, epidural space or subarachnoid space. Therapies that require a continuous rate of in
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-1682-2024·2024-08-14

    Wiers Farm Organic Cucumbers Recalled Due to Listeria Contamination

    Wiers Farm is recalling organic cucumbers due to Listeria monocytogenes contamination. Affected consumers should not consume the product and may return it.

    Product
    Wiers Farm - Organic Cucumber packaged into 2 count trays - cases dependent on customer
    Category
    Food
    Distribution
    18 states
  • SevereFDA (Food)·F-1700-2024·2024-08-14

    Wiers Farm Eggplant Recalled Due to Listeria Contamination

    Wiers Farm is recalling eggplant packaged in 1lb cartons due to Listeria monocytogenes contamination. The recall affects 2390 cases distributed across 17 states.

    Product
    Wiers Farm - Eggplant packaged in 1lb cartons - case size dependent on customer
    Category
    Food
    Distribution
    18 states
  • SevereFDA (Food)·F-1675-2024·2024-08-14

    Wiers Farm cucumbers recalled for potential Listeria monocytogenes contamination

    Wiers Farm is recalling bagged whole salad cucumbers due to potential Listeria monocytogenes contamination. Affected products were distributed to 18 states; consumers should not consume them and should return them to the store.

    Product
    Wiers Farm - Whole Salad Cucumbers bagged in 2lb plastic bags, 10 bags per carton
    Category
    Food
    Distribution
    18 states
  • SevereFDA (Food)·F-1646-2024·2024-08-14

    SAVPAK Duro Plastic Bags Recalled for Undeclared Wheat Allergen

    SAVPAK Duro 8oz plastic bags distributed in Texas are being recalled because they contain wheat that is not declared on the label. Consumers with wheat allergies should stop using the product immediately.

    Product
    SAVPAK Duro 10x10, 8oz plastic bag, DISTRIBUTED BY: Southcoast Product Inc. Dallas, Texas 75215; UPC 29661 00076.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1670-2024·2024-08-14

    Peanut Butter Snack Mix Recalled for Potential Salmonella Contamination

    Palmer & Company is recalling Freshness Guaranteed Peanut Butter Snack Mix due to potential salmonella contamination. The recall affects 12oz and 4.5oz packages distributed nationwide in the United States and Canada.

    Product
    1. Freshness Guaranteed Peanut Butter Snack Mix, Net Wt 12oz, UPC 78742 03912, 8/12oz case 2. Peanut Butter Snack Mix, Net Wt 4.5oz to go container, Distributed by: Kwik Trip Inc; UPC 39779 00424, 12/4.5oz case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1688-2024·2024-08-14

    Wiers Farm Habanero Peppers Recalled for Listeria Contamination

    Wiers Farm Inc is recalling habanero peppers sold in 1-pound cartons across 17 states due to potential Listeria monocytogenes contamination. The recall involves 441 cases with lot numbers 240705 through 240712.

    Product
    Wiers Farm - Habanero Peppers packaged into 1lb carton - 3lb per case
    Category
    Food
    Distribution
    18 states
  • SevereFDA (Food)·F-1647-2024·2024-08-14

    SAVPAK Duro Rueda 8oz Contains Undeclared Wheat Allergen

    SAVPAK Duro Rueda 8oz packages distributed in Texas contain undeclared wheat allergen. Consumers with wheat allergies or celiac disease should not consume this product.

    Product
    SAVPAK Duro Rueda 8oz, plastic bag, DISTRIBUTED BY: Southcoast Produce Inc. Dallas, Texas 75215; UPC 29661 00073
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1697-2024·2024-08-14

    Wiers Farm Butternut Squash Recalled for Listeria Monocytogenes

    Wiers Farm Inc is recalling Butternut Squash in 1-pound cartons due to potential Listeria monocytogenes contamination. Lot numbers 240705 through 240712 are affected.

    Product
    Wiers Farm - Butternut Squash packaged in 1lb cartons - case size dependent on customer
    Category
    Food
    Distribution
    18 states
  • SevereFDA (Food)·F-1661-2024·2024-08-14

    Sunny Select Strawberry Yogurt Coated Pretzels Recalled for Salmonella Risk

    Palmer & Company is recalling Sunny Select Strawberry Yogurt Coated Pretzels (10 oz, UPC 9848796055) distributed nationwide in the US and Canada due to potential salmonella contamination.

    Product
    Sunny Select Strawberry Yogurt Coated Pretzels, Net Wt. 10 oz, UPC 9848796055, 12/10oz case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1656-2024·2024-08-14

    Yogurt-Covered Pretzel Recall Due to Potential Salmonella Contamination

    Palmer & Company is recalling multiple yogurt-covered pretzel products distributed nationwide due to potential salmonella contamination. Consumers should not consume these products.

    Product
    1. Palmer Candy Classic Yogurt Pretzels, Net Wt 28 lbs, UPC 77232 10847 2. Sweet Smiles Yogurt Covered Pretzels, Net Wt. 3.25oz, UPC 77232 13641, 8/3.25oz case 3. Sconza Chocolates Yogurt Pretzels, Net Wt 14lbs, UPC 004166882015 4. Sunny Select Vanilla Yogurt Coated Pretzels, Net
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1663-2024·2024-08-14

    Palmer Patriotic Munchy Medley Recalled for Potential Salmonella Contamination

    Palmer & Company is recalling Palmer Patriotic Munchy Medley candy nationwide in the United States and Canada due to potential salmonella contamination.

    Product
    Palmer Patriotic Munchy Medley, Net Wt 15oz, UPC 7723237060, 12/15oz case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1689-2024·2024-08-14

    Green Bell Peppers Recalled for Listeria monocytogenes Contamination

    Wiers Farm green bell peppers packaged in 1-pound cartons are being recalled due to potential Listeria monocytogenes contamination. Affected lot numbers are 240705 through 240712, distributed across 17 states.

    Product
    Wiers Farm - Green Bell Pepper packaged into 1lb carton - cases size dependent on customer
    Category
    Food
    Distribution
    18 states
  • SevereFDA (Food)·F-1685-2024·2024-08-14

    Wiers Farm Jalapenos Recalled for Potential Listeria Contamination

    Wiers Farm jalapenos in 8oz bags are being recalled due to potential Listeria monocytogenes contamination. The recall affects 5,331 cases distributed across 16 states.

    Product
    Wiers Farm - Jalapenos packaged into 8oz bags - case size dependent on customer
    Category
    Food
    Distribution
    18 states
  • HighFDA (Devices)·Z-2495-2024·2024-08-14

    BD PYXIS Medication Cabinet Software Defect Causes Incorrect Restock Labels

    A software issue in BD PYXIS automated medication dispensing cabinets can cause restock labels to print with incorrect bin numbers. Four units are affected nationwide.

    Product
    BD PYXIS MEDBANK TWR MN CR-4HH-1FH-4FM-P, REF: 169-90 containing software version 3.9.1.9
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2520-2024·2024-08-14

    Medical Procedure Kit Recalled Over Potential Sterilization Compromise

    American Contract Systems is recalling Special Procedure Pack convenience kits due to insufficient aeration time during sterilization, which may have compromised sterility. Distributed in California, Kansas, Maine, Minnesota, Missouri, Nebraska, and South Dakota.

    Product
    American Contract Systems Special Procedure Pack convenience kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1649-2024·2024-08-14

    Premo Meat Lovers Recall Due to Potential Salmonella Contamination

    Premo Meat Lovers 7oz packages are being recalled due to potential Salmonella contamination. Affected products have a Best By Date of 7/13/24 and Lot Code 25202406.

    Product
    Premo Meat Lovers 7oz, clear plastic, UPC 612510093832, 4 retail packages per wholesale case
    Category
    Food
    Distribution
    16 states
  • HighFDA (Devices)·Z-2485-2024·2024-08-14

    Automated medication cabinet software prints incorrect bin labels

    The BD PYXIS MEDBANK MINI automated dispensing cabinet software may print incorrect bin locations on restock labels, potentially causing medications to be placed in wrong locations.

    Product
    BD PYXIS MEDBANK MINI CR-2HH-1FH-P, REF: 169-114 containing software version 3.9.1.9
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1724-2024·2024-08-14

    Panaderia Guatemex Gusano Bread Recalled for Undeclared Soy Allergen

    Panaderia Guatemex is recalling Gusano bread because it contains undeclared soy. People with soy allergies should not consume this product and should return it to the store.

    Product
    Panaderia Guatemex - Gusano packaged in plastic bag
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-2480-2024·2024-08-14

    MRI System Software Issue Can Overheat Implanted Medical Devices

    GE HealthCare recalled 23 SIGNA Victor MRI systems due to a software issue that can cause MR conditional implants to overheat. The defect occurs under specific imaging mode and configuration combinations.

    Product
    SIGNA Victor, with affected software versions: MR30.1; Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2459-2024·2024-08-14

    SIGNA Architect MRI System Software Can Exceed Implant Heating Limits

    GE Medical Systems is recalling SIGNA Architect MRI systems in which software may allow B1+ radiofrequency exposure to exceed user-prescribed limits during certain T2 FLAIR imaging sequences, risking MR-conditional implant overheating.

    Product
    SIGNA Architect, with affected software versions: DV26.0 to DV26.3, DV27.0 to DV27.3, DV28.0 to DV28.5, DV29.0, DV29.1, DV29.2, MR30.0, MR30.1; Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2532-2024·2024-08-14

    FDA Recalls CryoPatch Cardiac Tissue Grafts Due to Invalid Test Results

    Artivion has recalled CryoPatch SG cardiac tissue patches used in pulmonary surgeries due to approval and release with invalid test results. Patients who received implants should consult their healthcare provider.

    Product
    (1) CryoPatch SG Pulmonary Human Cardiac Hemi-Artery - Artery Patch, SGPH00 Cryopreserved Decellularized Cardiac Tissue Allograft Prepared with SynerGraft (SG) Technology; and (2) CryoPatch SG Pulmonary Human Cardiac Branch Patch, SGP020, Cryopreserved Decellularized Cardiac Tis
    Category
    Medical Device
    Distribution
    Distributed nationwide