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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30826–30850 of 39756

  • SevereFDA (Devices)·Z-2203-2014·2014-08-20

    Gambro Recalls Prismaflex M150 Dialysis Sets Due to Connector Breakage

    Gambro Renal Products is recalling Prismaflex M150 dialysis sets because connector breakages can cause liquid or blood to leak.

    Product
    Prismaflex M150. Product number 109990. Each set is packaged in a plastic pouch, 4 pouches per carton box
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2155-2014·2014-08-20

    Cardiovascular Systems Recalls Diamondback 360 Peripheral Orbital Atherectomy System

    Cardiovascular Systems, Inc. is recalling 48 Diamondback 360 Peripheral Orbital Atherectomy Systems because the saline sheath may crack or fracture, releasing particulate during use.

    Product
    CSI Cardiovascular Systems, Inc., Diamondback 360 Peripheral Orbital Atherectomy System, Model Number DBP-125MICRO145, Part Number 7-10003. The Diamondback 360 Peripheral Orbital Atherectomy System is a percutaneous orbital atherectomy system indicated for use as therapy in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2209-2014·2014-08-20

    Medical Positioning Rapid Response HUT Table Recalled for Malfunction Risk

    Medical Positioning Inc is recalling two Model # 1019 HUT tables due to a component defect that may cause the table to drop into the Trendelenburg position more rapidly than normal.

    Product
    Medical Positioning Rapid Response HUT table, Powered Medical Examination table, Model # 1019. Product Usage: Used to conduct syncope examinations.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2202-2014·2014-08-20

    Gambro Recalls Prismaflex M100 Dialysis Sets Due to Connector Breakage

    Gambro Renal Products is recalling Prismaflex M100 dialysis sets because connector breakages can cause leakage of liquid or blood.

    Product
    Prismaflex M100. Product number 106697. Each set is packaged in a plastic pouch, 4 pouches per carton box
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2199-2014·2014-08-20

    Gambro Recalls Prisma M100 PRE Pump Infusion Sets Due to Connector Breakage

    Gambro Renal Products is recalling Prisma M100 PRE pump infusion sets because connector breakages can cause liquid or blood to leak.

    Product
    Prisma M100 PRE pump infusion set. Product number 107791. Each set is packaged in a plastic pouch, 4 pouches per carton box
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Drugs)·D-1538-2014·2014-08-20

    Teva Recalls Carbidopa and Levodopa Tablets Due to Potential Superpotency

    Teva Pharmaceuticals USA is recalling one lot of Carbidopa and Levodopa Tablets USP, 25mg/100mg, due to the potential for superpotent tablets.

    Product
    Carbidopa and Levodopa Tablets USP, 25mg/100mg, 1000 count bottle, Rx only, Manufactured in Israel by Teva Pharmaceutical IND, LTD., Jeruselem, Israel, for Teva Pharmaceuticals USA, Sellersville, PA, NDC 0093-0293-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2206-2014·2014-08-20

    Gambro Recalls PrisMARS Kits Due to Connector Breakage and Leakage

    Gambro Renal Products is recalling PrisMARS Kits because connector breakages can cause liquid or blood to leak.

    Product
    PrisMARS Kit (component of MARS Treatment Kit Type 1115/1 PrisMARS US), 1 MARS Treatment Kit per carton box, Product Number 800480, Batch
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·14V508000·2014-08-19

    NABI Recalls 2014 BRT and LFW Buses Due to Fuel Filter Defect

    NABI is recalling 35 model year 2014 BRT and LFW transit buses because a fuel filter defect may cause the engine to stall without warning, increasing crash risk.

    Product
    NABI — NABI BRT, LFW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V504000·2014-08-18

    Dakota Air Ride Trailers Recalled for Suspension Pivot Bolt Failure Risk

    Dakota Trailer Manufacturing is recalling 2014 Air Ride Grain and Side Dump trailers because suspension pivot bolts may fail, potentially causing the axle to separate and increasing crash risk.

    Product
    DAKOTA GRAIN — DAKOTA GRAIN, DAKOTA SIDE DUMP AIR RIDE GRAIN, AIR RIDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V507000·2014-08-18

    Jerr-Dan Recalls Ford Super Duty Trucks Due to Fire Risk

    Jerr-Dan is recalling 2009-2014 Ford F-350, F-450, and F-550 Super Duty trucks modified with specific PTO assemblies. Oil leaks from the PTO pressure switch may soak the exhaust thermal blanket, increasing fire risk.

    Product
    FORD — FORD F-350 SUPER DUTY, F-550 SUPER DUTY, F-450 SUPER DUTY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V505000·2014-08-18

    Spartan Emergency Vehicles Recalled for Fuel Filter Defect

    Spartan is recalling 2013-2015 emergency vehicles and chassis because fuel filters may separate, causing the engine to stall without warning.

    Product
    SPARTAN — SPARTAN SB, GLADIATOR, METROSTAR, MM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V506000·2014-08-18

    Winnebago Vista and Itasca Sunstar Motorhomes Recalled for Fire Risk

    Winnebago is recalling 2015 Vista and Itasca Sunstar motorhomes because a missing damper plate could allow air to blow out the range flame, potentially causing a propane fire.

    Product
    WINNEBAGO — WINNEBAGO VISTA, ITASCA SUNSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·053-2014·2014-08-15

    Whole Foods Recalls Ground Beef Due To Possible E. Coli O157:H7 Contamination

    Whole Foods Market is recalling 368 pounds of ground beef products in Massachusetts due to possible E. coli O157:H7 contamination linked to three confirmed illnesses.

    Product
    Massachusetts Firm Recalls Ground Beef Products Due To Possible E. Coli O157:H7 Contamination
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·14V503000·2014-08-15

    Altec Recalls Aerial Devices and Digger Derricks Due to Fire Risk

    Altec is recalling 2000-2013 Aerial Devices and Digger Derricks because a battery equalizer component may conduct electricity and cause a fire.

    Product
    ALTEC — ALTEC AERIAL DEVICE, DIGGER DERRICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V502000·2014-08-14

    Jayco Recalls 2014-2015 Precept Motorhomes Due to Fire Risk

    Jayco is recalling 2014-2015 Precept motorhomes because damaged seat wiring may short and cause a fire. Owners should contact dealers for free repairs.

    Product
    JAYCO — JAYCO PRECEPT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2302-2014·2014-08-13

    Hot Mama's Foods Recalls Hummus Due to Listeria Concerns

    Hot Mama's Foods is recalling approximately 14,860 pounds of hummus and dip products due to concerns about possible Listeria monocytogenes.

    Product
    Spicy Yellow Lentil Hummus sold under the Eat Well Embrace Life brand and packaged in a transparent plastic tub with a net weight of 10 oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2298-2014·2014-08-13

    Hot Mama's Foods Recalls Chipotle Hummus Due to Listeria Concerns

    Hot Mama's Foods is recalling Chipotle Hummus sold under the Giant Eagle Market District brand due to concerns about possible Listeria monocytogenes.

    Product
    Chipotle Hummus sold under the Giant Eagle Market District brand and packaged in a transparent plastic tub with a net weight of 8 oz (227 g).
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2301-2014·2014-08-13

    Hot Mama's Foods Recalls Hummus and Dip Products for Listeria Concerns

    Hot Mama's Foods is recalling approximately 14,860 pounds of hummus and dip products due to concerns about possible Listeria monocytogenes.

    Product
    5 Layer Fiesta Dip sold under the Trader Joe's brand and packaged in a transparent plastic tub with a net weight of 11.5 oz (326 g) or 24 oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2291-2014·2014-08-13

    KIND Recalls Multiple Protein Bars Due to Potential Peanut Presence

    KIND, LLC is recalling several protein bar varieties due to the potential presence of peanut protein. The recall covers 12,190 cases distributed nationwide and in Mexico.

    Product
    STRONG & KIND Roasted Jalapeno Almond Protein Bar, 45g, packaged in a green, black and transparent wrapper. Sold individually or packaged in a box of 4 or 12.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2292-2014·2014-08-13

    KIND Recalls Multiple Protein Bars Due to Potential Peanut Presence

    KIND, LLC is recalling several varieties of KIND and Strong & KIND bars due to the potential presence of peanut protein.

    Product
    STRONG & KIND Honey Mustard Almond Protein Bar, 45g, packaged in a yellow, black and transparent wrapper. Sold individually or packaged in a box of 4 or 12.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2300-2014·2014-08-13

    Hot Mama's Foods Recalls Edamame Hummus for Listeria Concerns

    Hot Mama's Foods is recalling Trader Joe's Edamame Hummus due to possible Listeria monocytogenes contamination.

    Product
    Edamame Hummus sold under the Trader Joe's brand and packaged in a transparent plastic tub with a white lid and with a net weight of 8 oz (227 g).
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2297-2014·2014-08-13

    Hot Mama's Foods Recalls Hummus Due to Listeria Concerns

    Hot Mama's Foods is recalling approximately 14,860 pounds of hummus and dip products due to concerns about possible Listeria monocytogenes.

    Product
    Roasted Red Pepper Hummus sold under the Archer Farms brand and packaged in a transparent plastic tub with a net weight of 17 oz (1 lb. 1 oz).
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2299-2014·2014-08-13

    Hot Mama's Foods Recalls Garlic Hummus Due to Listeria Concerns

    Hot Mama's Foods is recalling approximately 14,860 pounds of hummus and dip products due to concerns about possible Listeria monocytogenes.

    Product
    Garlic Hummus sold under the Giant Eagle Market District brand and packaged in a transparent plastic tub with a net weight of 8 oz (227 g).
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2295-2014·2014-08-13

    Hot Mama's Foods Recalls Archer Farms Hummus Due to Listeria Concerns

    Hot Mama's Foods is recalling Archer Farms Traditional Hummus due to concerns about possible Listeria monocytogenes contamination.

    Product
    Traditional Hummus sold under the Archer Farms brand and packaged in either a transparent plastic tub or a white plastic tub with a net weight respectively of 10 oz (283 g) or 2 lb.
    Category
    Food
    Distribution
    Distributed nationwide