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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34001–34025 of 39756

  • SevereFDA (Food)·F-1847-2013·2013-08-28

    Harmony Chai Rooibos Chai Recalled for Improper Processing

    Harmony Chai is recalling 22 oz and 64 oz bottles of decaffeinated Rooibos Chai because the product was not properly processed.

    Product
    Acidified Tea in a glass bottle with a multi-colored, stick-on label that reads in part: " HARMONY Chai Decaffeinated Fresh brewed on Orcas Island, WA Rooibos Chai 22oz. (624,25ml)***Ingredients: water, Organic Raw Sugar, Rooibos Tea, cloves, cinnamon, Ginger, secret spices…
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1829-2013·2013-08-28

    NuGo Dark Mint Chocolate Chip Bars Recalled for Undeclared Milk

    NuGo Nutrition HQ is recalling Dark Mint Chocolate Chip bars because they may contain undeclared milk, posing a risk to people with milk allergies.

    Product
    NuGo Dark Mint Chocolate Chip, 1.59 oz (45g) Non-Dairy
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1831-2013·2013-08-28

    NuGo Dark Pretzel Non-Dairy Snack Recalled for Undeclared Milk

    NuGo Nutrition HQ is recalling Dark Pretzel Non-Dairy snacks because they may contain undeclared milk, a major allergen.

    Product
    NuGo Dark Pretzel 1.59 oz (45g) Non-Dairy Non-Dairy
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V383000·2013-08-28

    Toyota Recalls RAV4 and Lexus HS 250h for Rear Suspension Defect

    Toyota is recalling 2006-2011 RAV4 and 2010 Lexus HS 250h vehicles because rear tie rods may fail, causing loss of vehicle control.

    Product
    LEXUS — LEXUS, TOYOTA HS 250 HYBRID, RAV4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1825-2013·2013-08-28

    NuGo Free Dark Chocolate Crunch Recalled for Undeclared Milk

    NuGo Nutrition HQ is recalling NuGo Free Dark Chocolate Crunch bars because they may contain undeclared milk, posing a risk to consumers with milk allergies.

    Product
    NuGo Free Dark Chocolate Crunch, 1.59 oz (45g) Non-Dairy
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1982-2013·2013-08-28

    EndoGastric Solutions Recalls EsophyX2 Devices Due to Tissue Mold Control Loss

    EndoGastric Solutions is recalling EsophyX2 devices because of reports of loss of tissue mold control, which required surgical removal in one case.

    Product
    EndoGastric Solutions EsophyX2 Device with Serosa Fastener and Accessories. Models R2001 and R2002. Indicated for the treatment of symptomatic chronic gastroesophageal reflux disease.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·13E049000·2013-08-27

    Trans/Air Recalls Compressor Mount Kits for Ford Engines

    Trans/Air is recalling specific Compressor Mount Kits installed on Ford 5.4 or 6.8-liter engines due to a risk of alternator harness damage, vehicle stalling, or fire.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V382000·2013-08-27

    Honda Recalls 2013 Odyssey and Pilot Vehicles for Engine Piston Defect

    Honda is recalling 2013 Odyssey and Pilot vehicles because engine pistons may have insufficient hardness, leading to premature wear and potential engine stalling.

    Product
    HONDA — HONDA ODYSSEY, PILOT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1809-2013·2013-08-21

    Crave Brothers Farmstead Cheese Recalled Due to Listeria Investigation

    Crave Brothers Farmstead Cheese is recalling specialty cheese products while regulatory agencies investigate a potential Listeria monocytogenes contamination.

    Product
    Crave Brothers Farmstead Classics Les Freres Semi-Soft French Style Cheese, LF225. 2.5 lb wheel packaged in cheese paper. Two 2.5 lbs wheels in a case.
    Category
    Food
    Distribution
    9 states
  • CriticalFDA (Food)·F-1810-2013·2013-08-21

    Crave Brothers Petit Frere Cheese Recalled Due to Listeria Investigation

    Crave Brothers Farmstead Cheese is recalling Petit Frere Soft Ripened Cheese because of a multi-state Listeria monocytogenes investigation.

    Product
    Crave Brothers Farmstead Classics Petit Frere Soft Ripened Cheese, PF88. Net Wt. 8 oz. (227g). Packaged in cheese paper and sold inside a wooden box. Eight 8 oz wheels per case.
    Category
    Food
    Distribution
    9 states
  • CriticalFDA (Food)·F-1807-2013·2013-08-21

    Gold Star Herring Fillets Recalled for Listeria Contamination

    Gold Star Smoked Fish Corp. is recalling RYBACKA WIES brand Herring Fillets in Oil due to Listeria monocytogenes contamination found by New York State sampling.

    Product
    RYBACKA WIES brand HERRING FILLETS IN OIL (MATJES SLEDZ W OLEJU), Net Wt. 17.6 oz. (500g), UPC 0 21143 24122 8, Distributed By Gold Star, Inc., Brooklyn, NY 11231 --- The product is vacuum packed in a sealed plastic package.
    Category
    Food
    Distribution
    11 states
  • CriticalFDA (Food)·F-1805-2013·2013-08-21

    Brach's Chocolate Malted Milk Balls Recalled for Undeclared Peanuts and Brazil Nuts

    Ferrara Candy Company is recalling Brach's Chocolate Malted Milk Balls because they may contain undeclared peanuts and Brazil nuts.

    Product
    Chocolate malted milk balls packaged in 6 lbs. bags and each case contains 3 x 6 lbs. bags; BEST BY 04/17/14; BRCH CHOC
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1811-2013·2013-08-21

    Crave Brothers Petit Frere Cheese Recalled Over Listeria Investigation

    Crave Brothers is recalling Petit Frere with Truffles Cheese due to a multi-state Listeria monocytogenes investigation.

    Product
    Crave Brothers Farmstead Classics Petit Frere with Truffles Cheese, PF88T. Net Wt. 8 oz. (227g). Packaged in cheese paper and sold inside a wooden box. Eight 8 oz. wheels per case.
    Category
    Food
    Distribution
    9 states
  • CriticalFDA (Devices)·Z-1897-2013·2013-08-21

    Nova Max Glucose Test Strips Recalled for False High Readings

    Nova Biomedical Corporation is recalling Nova Max Glucose Test Strips due to reports of false abnormally high glucose readings.

    Product
    Nova Max Glucose Test Strips (50 Count Retail) Catalog Number: 43437 Product Usage: The Nova Max Glucose Test Strips are for use with the Nova Max Family of Glucose Monitors (Nova Max, Nova Max Plus, Nova Max Link, BD Logic and Paradigm Link). These monitors are intended…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1899-2013·2013-08-21

    Nova Max Glucose Test Strips Recalled for False High Readings

    Nova Biomedical is recalling 721,810 Nova Max Glucose Test Strips because they may produce false abnormally high glucose readings.

    Product
    Nova Max Glucose Test Strips (10 Count Boxed) Catalog Number: 43590 Product Usage: The Nova Max Glucose Test Strips are for use with the Nova Max Family of Glucose Monitors (Nova Max, Nova Max Plus, Nova Max Link, BD Logic and Paradigm Link). These monitors are intended to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-858-2013·2013-08-21

    Pallimed Recalls Alprostadil Injection Due to Sterility Assurance Concerns

    Pallimed Solutions is recalling 408 vials of Alprostadil IN NS Injection nationwide because FDA inspectional findings raised concerns about sterility assurance.

    Product
    Alprostadil IN NS Injection, compounded by Pallimed Solutions Pharmacy, Woburn, MA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-884-2013·2013-08-21

    Dr. Reddy's Recalls Ranitidine Tablets Due to Microbial Contamination

    Dr. Reddy's is recalling specific lots of OTC Ranitidine Hydrochloride tablets because raw material tested positive for Pseudomonas sp.

    Product
    Ranitidine Hydrochloride Tablets, USP, 150 mg, OTC, a) Equate brand Maximum Strength Acid Reducer, 65 count bottle Dist. By: Wal-Mart Stores, Inc., Bentonville, AR 72710, NDC 49035-404-61 b)Equaline brand maximum strength heartburn relief, , DISTRIBUTED BY SUPERVALU INC., EDEN…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-886-2013·2013-08-21

    Sanofi Recalls Subpotent Rifadin Capsules Due to Low Fill

    Sanofi-Synthelabo is recalling 998 bottles of Rifadin (rifampin) capsules because some capsules contained less medication than labeled.

    Product
    Rifadin (rifampin) capsules, USP, 150 mg, 100-count capsules per bottle, Manufactured by: Fabrique par Sanofi-Aventis Canada Inc., Laval, Quebec, Canada H7L4A8, DIN # 02091887
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1900-2013·2013-08-21

    Nova Max Glucose Test Strips Recalled for False High Readings

    Nova Biomedical is recalling Nova Max Glucose Test Strips because they may produce false abnormally high glucose readings, potentially affecting diabetes management.

    Product
    Nova Max Glucose Test Strips (100 Count Retail Canada)Catalog Number: 43955 Product Usage: The Nova Max Glucose Test Strips are for use with the Nova Max Family of Glucose Monitors (Nova Max, Nova Max Plus, Nova Max Link, BD Logic and Paradigm Link). These monitors are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-857-2013·2013-08-21

    Pallimed Acetylcysteine Ophthalmic Solution Recalled for Sterility Concerns

    Pallimed Solutions is recalling Acetylcysteine Ophthalmic Solution due to FDA inspectional findings regarding quality control and sterility assurance.

    Product
    Acetylcysteine Ophthalmic Solution, compounded by Pallimed Solutions Pharmacy, Woburn, MA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-878-2013·2013-08-21

    Pallimed Recalls Testosterone Cypionate Injection Due to Sterility Concerns

    Pallimed Solutions is recalling 597 vials of compounded Testosterone Cypionate Injection nationwide due to FDA inspectional findings regarding sterility assurance.

    Product
    Testosterone Cypionate Injection,compounded by Pallimed Solutions Pharmacy, Woburn, MA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-866-2013·2013-08-21

    Pallimed Solutions Recalls Dexamethasone PF Due to Sterility Concerns

    Pallimed Solutions is recalling Dexamethasone PF compounded in Woburn, MA, due to FDA inspectional findings regarding quality control and sterility assurance.

    Product
    Dexamethasone PF, compounded by Pallimed Solutions Pharmacy, Woburn, MA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1966-2013·2013-08-21

    Medtronic Recalls Pediatric Arterial Filters Due to Potential Media Breach

    Medtronic is recalling 148 Affinity Pediatric Arterial Filters because a small breach in the filter media may allow unwanted particulate or gaseous emboli to pass through, posing a risk of serious injury or death to pediatric patients.

    Product
    Medtronic Affinity Pediatric Arterial Filter, model number S4014, sterilized using ethylene oxide. Recall Update 9/6/13: Medtronic, Red cross Infant Pack 1/B, South-Africa, REF M272403C, Sterile EO. The Affinity Pediatric Arterial Filters are single-use, sterile…
    Category
    Medical Device
    Distribution
    2 states