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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19551–19575 of 39605

  • SevereNHTSA·17V625000·2017-10-06

    Subaru Recalls 2015 WRX Models Due to Subwoofer Wiring Fire Risk

    Subaru is recalling 9,178 2015 WRX vehicles because trunk items may cause subwoofer wiring to short, potentially leading to overheating and fire.

    Product
    SUBARU — SUBARU WRX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V632000·2017-10-06

    John Evans Recalls 2017-2018 Flatbed Trailers Due to Brake Defect

    John Evans is recalling 2017-2018 Flatbed trailers because air brake diaphragms may degrade, causing emergency brakes to engage and increasing crash risk.

    Product
    EVANS — EVANS FLATBED TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V630000·2017-10-05

    Cheetah Trailer Chassis Recalled for Air Brake Diaphragm Defect

    Cheetah Chassis Corporation is recalling specific 2017-2018 trailer chassis models because air brake diaphragms may degrade, causing emergency brakes to engage unexpectedly.

    Product
    CHEETAH — CHEETAH MAXIMIZER CHASSIS, TANK CHASSIS, BRIDGEMASTER CHASSIS, EXTENDABLE CHASSIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V622000·2017-10-05

    Audi Recalls 2013-2016 Models Due to Auxiliary Heater Fire Risk

    Volkswagen Group of America is recalling 216,913 Audi A5, A4 Allroad, and Q5 vehicles because contact corrosion in the auxiliary heater connector may cause wires to overheat or melt, increasing the risk of a fire.

    Product
    AUDI — AUDI A5, A4 ALLROAD, Q5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-3362-2017·2017-10-04

    Lantana White Bean Hummus Recalled for Listeria Risk

    House Of Thaller Inc is recalling Lantana White Bean Hummus because pine nuts may be contaminated with Listeria monocytogenes.

    Product
    LANTANA White Bean HUMMUS NET WT. 10 oz (283g)
    Category
    Food
    Distribution
    32 states
  • CriticalFDA (Food)·F-3607-2017·2017-10-04

    Country Fresh Fajita Mix Recalled for Listeria Contamination Risk

    Country Fresh Products is recalling 6-oz Fajita Mix packages due to potential Listeria monocytogenes contamination. The product was distributed in five southern states.

    Product
    Fajita Mix, 6-oz. packaged in a clamshell
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-3605-2017·2017-10-04

    Country Fresh Products Recalls Creole Mix Due to Listeria Risk

    Country Fresh Products is recalling 6-oz. packages of Creole Mix due to potential contamination with Listeria monocytogenes.

    Product
    Creole Mix, 6-oz. packaged in a clamshell
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-3585-2017·2017-10-04

    Marketside Classic Hummus with Pine Nuts Recalled for Listeria Risk

    House Of Thaller Inc is recalling Marketside Classic Hummus with Pine Nuts because the pine nuts may be contaminated with Listeria monocytogenes.

    Product
    Marketside CLASSIC HUMMUS WITH PINE NUTS NET WT. 10 oz (283g)
    Category
    Food
    Distribution
    32 states
  • CriticalFDA (Food)·F-3579-2017·2017-10-04

    Country Fresh Fajita Blend Recalled for Listeria Risk

    Country Fresh Products is recalling 12-oz Fajita Blend packages due to potential Listeria monocytogenes contamination. The product was distributed in five southeastern states.

    Product
    Fajita Blend, 12-oz. packaged in an overwrap
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-3580-2017·2017-10-04

    Country Fresh Stir Fry Vegetable Recalled for Listeria Risk

    Country Fresh Products is recalling 10-oz. Stir Fry Vegetable packages due to potential Listeria monocytogenes contamination.

    Product
    Stir Fry Vegetable, 10-oz. packaged in an overwrap
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-3361-2017·2017-10-04

    House Of Thaller Artisan Hummus Recalled for Listeria Risk

    House Of Thaller Inc is recalling Artisan Hummus Pine Nuts due to potential Listeria monocytogenes contamination.

    Product
    FRESH FOODS MARKET Artisan Humus Pine Nuts NET WT 10 oz (283g)
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Devices)·Z-3164-2017·2017-10-04

    Zimmer Biomet Recalls ECT Internal Fracture Fixation Drills

    Zimmer Biomet is recalling 4,423 ECT Internal Fracture Fixation Drills because raw material anomalies may increase the risk of instrument fracture during use.

    Product
    ECT Internal Fracture Fixation Drill 2.0 mm Diameter (.079 Inch), Item Number/EDI 00231802000, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3181-2017·2017-10-04

    Zimmer Biomet Recalls Orthopedic Surgical Drills and Screw Taps

    Zimmer Biomet is recalling 1,129 orthopedic surgical drills and screw taps due to raw material anomalies that may increase the risk of instrument fracture.

    Product
    Zimmer Periarticular Locking Plate System Drill Standard 2.7 mm Diameter, Item Number/EDI 00236020527, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3183-2017·2017-10-04

    Zimmer Biomet Recalls Orthopedic Drill Bits Due to Fracture Risk

    Zimmer Biomet is recalling specific orthopedic drill bits and screw taps because raw material anomalies may cause the instruments to fracture during use.

    Product
    ECT Internal Fracture Fixation Quick-Connect Drill 2.0 mm Diameter 12.5 cm Length, Item Number/EDI 00241002100, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3604-2017·2017-10-04

    Country Fresh Diced Green Pepper Recalled for Listeria Risk

    Country Fresh Products is recalling diced green peppers due to potential Listeria monocytogenes contamination. The product was distributed in five southeastern states.

    Product
    Green Pepper Diced, 6-oz. packaged in a clamshell
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Devices)·Z-3151-2017·2017-10-04

    Zimmer Biomet Recalls Orthopedic Surgical Drill Bits and Screw Taps

    Zimmer Biomet is recalling specific orthopedic surgical instruments due to a raw material anomaly that may increase the risk of instrument fracture during use.

    Product
    Zimmer Natural Nail System Calibrated Drill Long 4.3mm, Item Number/EDI 00249004443, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1177-2017·2017-10-04

    Pfizer Recalls Sterile Water for Injection Vials Due to Cracked Glass

    Pfizer is recalling 18,725 vials of Sterile Water for Injection due to cracked or chipped glass at the neck, which poses a non-sterility risk.

    Product
    Sterile Water for Injection, USP Single Dose 100 mL vials, Rx only, Manufactured by Hospira, Inc., Lake Forest, IL 60045 USA for Genentech, Inc., South San Francisco, CA 94080-4990. NDC 50242-901-24
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3196-2017·2017-10-04

    Zimmer Biomet Recalls Orthopedic Drill Bits Due to Fracture Risk

    Zimmer Biomet is recalling specific orthopedic drill bits and screw taps because raw material anomalies may increase the risk of instrument fracture during use.

    Product
    Drill Bit Quick-Connect 3.5 mm Diameter 110 mm Length, Item Number/EDI 00480611035, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V618000·2017-10-04

    Prevost Recalls Motor Coaches Due to Fuel Tank Cradle Defect

    Prevost is recalling 2008-2018 motor coaches because fuel tank cradles may loosen, causing the tank to fall off and increasing crash risk.

    Product
    PREVOST — PREVOST X3-45 VIP ENTERTAINER, X3-45 VIP, XL2, H3-45 VIP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3106-2017·2017-10-04

    Spectranetics Bridge Occlusion Balloon Catheter Recalled for Guidewire Issues

    Spectranetics is recalling Bridge Occlusion Balloon catheters because the guidewire may not pass through the device, potentially delaying treatment.

    Product
    Spectranetics Bridge Occlusion Balloon catheter, Sheath Compatibility 12F, Guidewire Compatibility 0.035in, Working Length 90cm, Balloon Outer Diameter 31mm, Balloon Length 80mm, Rx Only. Product Usage: It is a device used to occlude the vessel and prevent blood loss as the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3175-2017·2017-10-04

    Zimmer Biomet Recalls Straight Shank Drill Bits Due to Fracture Risk

    Zimmer Biomet is recalling 62 units of 4.0 mm Straight Shank Drill Bits because raw material anomalies may increase the risk of instrument fracture during use.

    Product
    Straight Shank Drill Bits 4.0 mm Diameter, Item Number/EDI 00231804006, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3202-2017·2017-10-04

    Zimmer Biomet Recalls Orthopedic Drill Bits Due to Fracture Risk

    Zimmer Biomet is recalling 150 nonsterile orthopedic drill bits because raw material anomalies may cause the instruments to fracture during use.

    Product
    Drill Bit Quick-Connect 4.5 mm Diameter 145 mm Length, Item Number/EDI 00480614545, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3199-2017·2017-10-04

    Zimmer Biomet Recalls Orthopedic Drill Bits Due to Fracture Risk

    Zimmer Biomet is recalling 15 nonsterile orthopedic drill bits because raw material anomalies may increase the risk of instrument fracture during use.

    Product
    Drill Bit Quick-Connect 3-Fluted 4.5 mm Diameter 195 mm Length, Item Number/EDI 00480719545, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3575-2017·2017-10-04

    Wegmans Dark Chocolate Cherry Cashew Granola Bars Recalled for Vitamin A

    Treehouse Foods is recalling Wegmans Dark Chocolate Cherry Cashew chewy granola bars because they may contain a higher concentration of Vitamin A than declared on the label.

    Product
    Wegmans Dark Chocolate Cherry Cashew chewy granola bars, 12-1.4OZ(40g) bars, Total Net Wt. 16.8OZ (1 LB 0.8OZ) 480g, UPC 77890-42230
    Category
    Food
    Distribution
    1 state