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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29651–29675 of 39756

  • SevereFDA (Devices)·Z-0180-2015·2014-12-17

    Covidien Recalls Puritan Bennett 980 Ventilators Due to Capacitor Failure

    Nellcor Puritan Bennett is recalling 324 Puritan Bennett 980 Ventilators because a capacitor component can fail, causing a dim screen and thermal odor.

    Product
    Covidien Puritan Bennett 980 Ventilator, Rx ONLY, Made in Ireland., Covidien LLC, USA. REF 980X1ENDIUU.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0707-2015·2014-12-17

    HeartLight Seafood Recalls Frozen Yellowfin Tuna Ground Meat

    Heartlight Seafood LLC is recalling 42,000 lbs of frozen yellowfin tuna ground meat due to potential high histamine levels.

    Product
    HeartLight Seafood brand Frozen Yellowfin Tuna Ground Meat (Thunnus albacares), IQF packed in a master carton of 10 x 1 lbs HDPE bags
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0296-2015·2014-12-17

    FDA Recalls Ondansetron Injection Vials Due to Sterility Concerns

    Fresenius Kabi USA is recalling 184,550 vials of Ondansetron Injection due to potential glass fractures and particles that compromise sterility.

    Product
    ONDANSETRON — ONDANSETRON (ONDANSETRON HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0708-2015·2014-12-17

    Whole Foods Market Vegan Pumpkin Pie Recalled for Undeclared Walnuts

    Whole Foods Market is recalling 1,144 vegan pumpkin pies because they contain walnuts that are not listed on the label.

    Product
    Whole Foods Market 9 inch Vegan Pumpkin Pie (32 oz) and 1/2 Vegan Pumpkin Pie (15 oz), packaged in both clear, clamshell packaging and brown, Kraft paper boxes. Distributed by Whole Foods Market. UPCs 24917101099 and 24917300699.
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-0507-2015·2014-12-17

    TomoTherapy Treatment System Recalled for Jaw Position Monitoring Failure

    TomoTherapy Incorporated is recalling 210 TomoTherapy Treatment Systems worldwide due to a software defect that may fail to monitor jaw position after an error, potentially leading to incorrect treatment delivery.

    Product
    TomoTherapy Treatment System with software versions 2.0.1 / 2.0.2 / 2.0.3/ (Hi:Art 5.0.1 / 5.0.2 / 5.0.3)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V801000·2014-12-17

    Ferrara Fire Custom Trucks Recalled for Fuel Filter Defect

    Ferrara is recalling 12 model year 2014 Fire Custom trucks because a fuel filter defect may cause the engine to stall without warning, increasing crash risk.

    Product
    FERRARA — FERRARA FIRE CUSTOM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0562-2015·2014-12-17

    PFM Medical Recalls ASEPT Drainage Kits for Bacterial Endotoxin Concerns

    PFM Medical is recalling ASEPT 600 ml Drainage Kits because they may exceed USP limits for bacterial endotoxin. The recall affects 1,470 units distributed in the US and abroad.

    Product
    ASEPT 600 ml Drainage Kit, Ref No. 622287, M7052 Product Usage: The ASEPT Drainage Kit is an accessory to be used to connect to the ASEPT Pleural or Peritoneal Drainage Catheter to drain fluid from the chest or abdomen.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0297-2015·2014-12-17

    Fresenius Kabi Recalls Cyanocobalamin Vials Due to Sterility Concerns

    Fresenius Kabi USA is recalling 240,550 vials of Cyanocobalamin Injection due to potential glass fractures and particles that compromise sterility.

    Product
    CYANOCOBALAMIN — CYANOCOBALAMIN (CYANOCOBALAMIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0523-2015·2014-12-17

    Siemens Mammomat Inspiration System Recalled for Potential Instability

    Siemens is recalling three Mammomat Inspiration systems because the workstation table may fall over if not secured, posing a risk of serious injury.

    Product
    Mammomat Inspiration system: Product Usage: mammography exams, screening, diagnosis, and stereotactic biopsies under the supervision of medical professionals. Mammographic images can be interpreted by either hard copy film or soft copy workstation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0621-2015·2014-12-17

    Wawona Packing Recalls Pluots, Peaches, Nectarines, and Plums for Listeria Risk

    Wawona Packing Company is recalling certain lots of pluots, peaches, nectarines, and plums packed in 2014 due to potential Listeria monocytogenes contamination.

    Product
    Pluot: Product of USA: Brand names: Sweet 2 Eat, Sweet 2 Eat Organic Orchard Perfect, Trader Joes, Sam's, Mrs. Smittcamp's, Harvest Sweet, Wawona, Costco, Sweet O. Brand names: Sweet 2 Eat, Orchard Perfect, Trader Joe's, Sam's, Mrs. Smittcamp's, Harvest…
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0590-2015·2014-12-17

    Smith & Nephew Recalls Legion Knee Prosthesis Due to Undersized Stem Taper

    Smith & Nephew is recalling 45 units of the Legion COCR Constrained Femoral Component because the stem taper is undersized and the gauge point is not deep enough.

    Product
    LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT, SIZE 5, RIGHT, REF 71426005, QTY 1, Smith & Nephew, knee prosthesis Usage:orthopedic.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0524-2015·2014-12-17

    Medtronic MiniMed Infusion Sets Recalled Due to Tubing Detachment Risk

    Medtronic MiniMed is recalling Silhouette and Sure-T infusion sets because tubing may detach, interrupting insulin delivery without an alarm.

    Product
    Medtronic MiniMed Silhouette and/or MiniMed Sure-T Infusion Sets; Paradigm Silhouette infusion sets: MMT-368, MMT-368600, MMT-371, MMT-373, MMT-377, MMT-377600, MMT378, MMT-378600, MMT-38 1, MMT-381 600, MMT-382, MMT-382600, MMT-383, MMT-383600, MMT384, & MMT384600. Sure-T…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0591-2015·2014-12-17

    Smith & Nephew Recalls Legion Knee Prosthesis Due to Undersized Stem Taper

    Smith & Nephew is recalling 23 units of the Legion COCR Constrained Femoral Component because the stem taper is undersized and the gauge point is not deep enough.

    Product
    LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT, SIZE 6, LEFT, REF 71426006, QTY 1, Smith & Nephew, knee prosthesis Usage:orthopedic.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0294-2015·2014-12-17

    Hospira Recalls Fentanyl Citrate Injection Due to Sterility Concerns

    Hospira Inc. is recalling Fentanyl Citrate Injection vials because improperly crimped flip-top seals may compromise sterility.

    Product
    FENTANYL CITRATE — FENTANYL CITRATE (FENTANYL CITRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V798000·2014-12-17

    Blue Bird Recalls 2015-2016 School Buses for Parking Brake Defect

    Blue Bird is recalling 2015-2016 Vision and All American school buses because a defective parking brake pedal assembly may fail to engage, increasing crash risk.

    Product
    BLUE BIRD — BLUE BIRD VISION, ALL AMERICAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V793000·2014-12-16

    Terex Advance Recalls 2013-2015 Concrete Mixer Trucks for Suspension Defect

    Terex Advance is recalling 2013-2015 Front Discharge Concrete Mixer Trucks because improperly secured nuts may cause the front axle leaf spring to partially disconnect, increasing crash risk.

    Product
    TEREX ADVANCE — TEREX ADVANCE FRONT DISCHARGE CONCRETE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V791000·2014-12-15

    Hino Recalls 2005-2015 Trucks Due to Parking Brake Wear

    Hino is recalling 2005-2015 NE8J, NF8J, and ND8J trucks because parking brake components may wear, causing the brake to release or fail to engage, increasing crash risk.

    Product
    HINO — HINO NE8J, NF8J, ND8J
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V787000·2014-12-12

    Ford Recalls 2005-2006 GT Vehicles for Air Bag Inflator Defect

    Ford is recalling 2005-2006 GT vehicles sold in high-humidity areas because the passenger air bag inflator may rupture during deployment, potentially causing serious injury.

    Product
    FORD — FORD GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0458-2015·2014-12-10

    ConMed Adult Radiotransparent Electrode Recall Due to Connection Failure Risk

    ConMed is recalling Adult Radiotransparent Electrodes because design changes to Philips AEDs may prevent connection, delaying therapy and risking patient death or serious injury.

    Product
    ADULT Radiotransparent Electrode, REF/Catalog Number 2516H-PC, Rx ONLY --- COMPARABLE TO PHILIPS MEDICAL HEARTSTART ELECTRODES PLUG STYLE CONNECTOR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0462-2015·2014-12-10

    ConMed Multifunction Electrodes Recalled for Connection Design Failure

    ConMed is recalling multifunction electrodes due to a design change that may prevent connection to Philips AEDs, potentially delaying therapy.

    Product
    CONMED ADULT R2 Multifunction Electrodes, REF/Catalog Number 3115-1751, Direct Connect to Philips Heartstart, Rx ONLY --- ASSEMBLED IN MEXICO -Intended for use during defibrillation, cardioversion, pacing, and ECG monitoring applications. This product is a single-use, disposable…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0595-2015·2014-12-10

    Oasis Brands Recalls Lacteos Santa Martha Cheese Due to Listeria

    Oasis Brands is voluntarily recalling Lacteos Santa Martha Queso Seco Centroamericano because Listeria monocytogenes was found in related products and environmental samples.

    Product
    Queso Seco Centroamericano (Cheese) in individually soft poly/plastic bags labeled in part: Lacteos Santa Martha Queso Seco Centroamericano Dry White Cheese Net Wt 1LB (16oz)
    Category
    Food
    Distribution
    4 states