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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36276–36300 of 39777

  • SevereNHTSA·12V491000·2012-10-10

    Toyota Recalls 2007-2009 Models for Power Window Switch Fire Risk

    Toyota is recalling approximately 2.5 million vehicles from 2007-2009 because power window switches may overheat and cause a fire.

    Product
    TOYOTA — TOYOTA, SCION, PONTIAC CAMRY, XD, CAMRY HYBRID, HIGHLANDER HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-004-2013·2012-10-10

    Carefusion Recalls ChloraPrep Skin Preparation Due to Sterility Failure

    Carefusion 213, LLC is recalling ChloraPrep One-Step skin preparation applicators because quarantined material failed sterility testing. The affected product was distributed in Illinois, Missouri, and New Jersey.

    Product
    ChloraPrep One-Step (2% w/v chlorhexidine gluconate and 70% v/v isopropyl alcohol) Patient Preoperative Skin Preparation, 3mL Applicators, 25 Applicators per Carton, Single Use, Latex Free, Applicator is STERILE if package is intact, NDC 54365-400-01.
    Category
    Medical Device
    Distribution
    3 states
  • SevereFDA (Food)·F-2443-2012·2012-10-10

    Gills Onions Recalls Diced Red Onions Due to Listeria Risk

    Gills Onions is recalling specific lots of diced red onions because they may be contaminated with Listeria monocytogenes.

    Product
    1/4" Diced Red Onions, 5lb, 2/5lb, 4/5lb; 3/8" Diced Red Onions, 2/5 lb, 4/5lb;
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1073-2012·2012-10-10

    Sadie's Salads Cream Slaw Recalled for Undeclared Egg and Soy Allergens

    Sadie's Salads is recalling Old Fashioned Cream Slaw because the label fails to declare egg and soybean oil allergens present in the mayonnaise.

    Product
    Sadie's Salads Old Fashioned Cream Slaw, 5 lb, 10 lb and 30 lb plastic tubs
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2479-2012·2012-10-10

    Zimmer Recalls Provisional Femoral Heads Due to Fit Issues

    Zimmer, Inc. is recalling specific provisional femoral heads used in hip surgery due to reports of improper fit with mating components.

    Product
    00780302201 MIS 12/14 Slotted Femoral Head Provisional -2X22 00780302202 MIS 12/14 Slotted Femoral Head Provisional +0X22 00780302203 MIS 12/14 Slotted Femoral Head Provisional +3.5X22 The provisional heads replicate final femoral implant geometry and are used to trial…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2449-2012·2012-10-10

    Triple B Recalls Sliced White Mushrooms Due to Listeria Risk

    Triple B Corporation is recalling 8 oz sliced white mushrooms due to potential Listeria monocytogenes contamination. The product was distributed in Idaho, Montana, and Washington.

    Product
    Sliced White Mushroom, Champ's Mushroom, net wt. 8 oz. The UPC is 0 33383 67600 5.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-2444-2012·2012-10-10

    Gills Onions Recalls Diced and Slivered Onions Due to Listeria Risk

    Gills Onions is recalling diced and slivered onions because they may be contaminated with Listeria monocytogenes.

    Product
    1/2" Diced Yellow Onions, 2/5lb, 4/5lb, 20lb. 1/4" Diced Yellow Onions, 1/5 lb, 2/5lb, 4/5lb. 1/8" Diced Yellow Onions, 4/5lb. 3/16" Diced Yellow Onions, 4/5lb. 3/8" Diced Yellow Onions, 1/5lb, 2/5lb, 4/5lb.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0010-2013·2012-10-10

    Daniella Mango Chunks Recalled for Potential Salmonella Contamination

    FreshPoint Central California is recalling Daniella brand mango chunks due to potential Salmonella Braenderup contamination. The product was distributed in California.

    Product
    Mango Chunks, 5# tub Distributed by FreshPoint Central California, Turlock, CA
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·12V487000·2012-10-05

    BMW Recalls 2,483 Motorcycles for Front Brake Fluid Foaming

    BMW is recalling 2,483 motorcycles because front brake fluid can foam, reducing braking capability and increasing crash risk.

    Product
    BMW — BMW K1300 S, K1200 R, K1200 R SPORT, K1200 S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V485000·2012-10-04

    Land Rover Recalls 2012 Range Rovers for Windshield Installation Defect

    Land Rover is recalling 2012 Range Rovers because windshields may have been installed incorrectly. This defect could cause the windshield to come loose in a crash, increasing injury risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1698-2012·2012-10-03

    FDA Recalls Hard Ten Days Capsules for Unapproved Sildenafil

    The FDA is recalling Hard Ten Days Capsules because they contain sildenafil, an unapproved active ingredient. Consumers should stop using the product.

    Product
    Hard Ten Days Capsule, 4500 mg, boxes of 6 packets, OTC, Developed by: American Federal International Living Creature Group and Tibet Gold Source Living Creature Engineering Limited Company, Unit 18, 55 Beijing Road Central, Lhasa, Tibet
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2390-2012·2012-10-03

    Gordon Food Service Recalls Pistachios Due to Potential Peanut Contamination

    Gordon Food Service is recalling shelled raw pistachios because they may be mis-packed with chopped peanuts, posing a risk to people with peanut allergies.

    Product
    Pistachios, Shelled Raw, 4 /2.5 Packed by Tropical Food Nut & Fruit- Orlando, FL 32811
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-2369-2012·2012-10-03

    True Nutrition Recalls Whey Protein Products for Undeclared Milk

    True Nutrition is recalling specific whey protein products because they contain undeclared milk, posing a risk to individuals with milk allergies.

    Product
    Whey Protein Isolate MicroFiltration, Net Weight: 1lb (454g)
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2398-2012·2012-10-03

    McClure's Apple Cinnamon Streusel Cake Recalled for Undeclared Walnuts

    McClure's Pies & Salads is recalling Apple Cinnamon Streusel Cakes because the ingredient list mentions nuts but fails to specifically identify walnuts.

    Product
    McClure's Pies & Salads, Inc. Apple Cinnamon Streusel Cake
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Drugs)·D-1700-2012·2012-10-03

    Japan Weight Loss Blue Capsules Recalled for Unapproved Sibutramine

    Vitaminbestbuy.com is recalling Japan Weight Loss Blue Capsules because they contain sibutramine, an unapproved drug ingredient.

    Product
    Japan Weight Loss Blue Capsules, 9 g (300 mg), 30 count box, Green algae lipotropic (fat dissolving) agent, OTC, Distributed by Vitaminbestbuy.com, Brewerton, NY
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2371-2012·2012-10-03

    True Nutrition Recalls Whey Protein Products for Undeclared Milk

    True Nutrition is recalling specific whey protein products because they contain undeclared milk, posing a risk to individuals with milk allergies.

    Product
    Hydrolyzed Whey Protein High Grade, Net Weight: 1lb (454g)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1686-2012·2012-10-03

    Baxter Recalls 5% Dextrose Injection Due to Chemical Contamination

    Baxter Healthcare is recalling 5% Dextrose Injection USP in AVIVA containers due to potential trace levels of cumene hydroperoxide.

    Product
    5% Dextrose Injection USP, packaged in a) 250 mL AVIVA Container, product code 6E0062, NDC 0338-6346-02; b) 500 mL AVIVA Container, product code 6E0063, NDC 0338-6346-03; Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015 USA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2437-2012·2012-10-03

    FDA Recalls Covidien Duet TRS Stapler Units Due to Injury Risk

    The FDA is recalling 268,022 units of the Covidien Duet TRS 60 3.5 mm Universal Articulating Single Use Loading Unit because the device may injure adjacent anatomical structures.

    Product
    Covidien Duet TRS 60 3.5 mm Universal Articulating Single Use Loading Unit. Product Code: DUET6035A. Single Use Loading Unit (SULU) tissue reinforcement stapler. The Endo GIA Universal Staplers with Duet TRS reloads have applications in abdominal, gynecologic and pediatric…
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2435-2012·2012-10-03

    FDA Recalls Covidien Duet TRS Stapler Units Due to Injury Risk

    The FDA is recalling 104,355 units of the Covidien Duet TRS 45 4.8 mm Universal Articulating Single Use Loading Unit because the device may injure adjacent anatomical structures.

    Product
    Covidien Duet TRS 45 4.8 mm Universal Articulating Single Use Loading Unit. Product Code: DUET4548A. Single Use Loading Unit (SULU) tissue reinforcement stapler. The Endo GIA Universal Staplers with Duet TRS reloads have applications in abdominal, gynecologic and pediatric…
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2462-2012·2012-10-03

    Varian Eclipse Treatment Planning System Recalled for Dose Calculation Error

    Varian is recalling Eclipse Treatment Planning Systems because a clock synchronization issue can cause incorrect dose calculations, potentially leading to under- or over-dosing of patients.

    Product
    Varian brand Eclipse Treatment Planning System, Model Number: H48; Eclipse 8.9 and 10.0 Reference/FSCA Identifier: CP-08922; Product is manufactured and distributed by Varian Medical Systems Inc., Palo Alto, CA The Eclipse Treatment Planning System (Eclipse TPS) is used to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2385-2012·2012-10-03

    Ready Pac Sweet Sunshine Platter Recalled for Salmonella Risk

    Ready Pac Foods is voluntarily recalling Sweet Sunshine Platters containing mangoes due to potential Salmonella Braenderup contamination.

    Product
    Ready Pac¿ Sweet Sunshine Platter, 37oz, UPC 7774524204, Use by dates 9/8/2012 or earlier and 9/6/2012 & 9/7/2012.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2378-2012·2012-10-03

    Ready Pac Recalls Fruit Mixes Due to Potential Salmonella Contamination

    Ready Pac Foods Inc is voluntarily recalling specific fruit mixes containing mangoes due to potential Salmonella Braenderup contamination.

    Product
    Fruit Mixes: 1) Dining In¿ Super Fruit Medley,10.5oz, UPC 1122508396, Use by date 9/6/2012; 2) Ready Pac¿ Super Fruit Blend, 6oz , UPC 7774523076, Use by Dates 9/8/2012 or earlier, 9/6/2012 & 9/7/2012; 3) Ready Pac¿ Super Fruit Medley, 10.5oz, UPC 7774523746, Use by dates…
    Category
    Food
    Distribution
    Distributed nationwide