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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17551–17575 of 39601

  • SevereFDA (Devices)·Z-2563-2018·2018-08-08

    Galt Medical Recalls Centeze Centesis Catheters Due to Bacterial Endotoxins

    Galt Medical Corporation is recalling 300 units of Centeze Centesis Catheters because they may contain unsafe levels of bacterial endotoxins introduced during manufacturing.

    Product
    Centeze Centesis Catheter, Catalog #: a) DRC-006-05, b) DRC-006-15,
    Category
    Medical Device
    Distribution
    19 states
  • SevereFDA (Food)·F-1798-2018·2018-08-08

    Sugar Foods Recalls Homestyle Seasoned Croutons Due to Whey Powder Contamination

    Sugar Foods Corporation is recalling 4 oz. pouches of Homestyle Seasoned Croutons because they were produced using recalled whey powder.

    Product
    Homestyle Seasoned Croutons: 4 oz. foil pouch Item # 73689 UPC 10083661736898 Sugar Foods Corporation 6190 E. Slauson Ave. Los Angeles, CA 90047
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-1804-2018·2018-08-08

    Sugar Foods Recalls Italian Seasoned Croutons Due to Whey Powder Contamination

    Sugar Foods Corporation is recalling 1 lb. foil pouches of Homestyle Italian Seasoned Croutons because they were made with recalled whey powder.

    Product
    Homestyle Italian Seasoned Croutons: 1 lb. foil pouch Item # 74384 Sugar Foods Corporation 6190 E. Slauson Ave. Los Angeles, CA 90047
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Drugs)·D-1021-2018·2018-08-08

    RemedyRepack Recalls Valsartan/HCTZ Tablets Due to Carcinogen Impurity

    RemedyRepack Inc. is recalling specific lots of Valsartan/HCTZ tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.

    Product
    Valsartan/HCTZ 320mg/12.5 mg tablet, 90-count bottle, Rx only, RemedyRepack, 625 Kolter Drive, Suite 4, Indiana, PA 15701
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Food)·F-1806-2018·2018-08-08

    Sugar Foods Recalls Garlic Butter Focaccia Crumbles Due to Whey Powder Issue

    Sugar Foods Corporation is recalling Garlic Butter and Black Pepper Focaccia Crumbles because they were made with recalled whey powder.

    Product
    Garlic Butter and Black Pepper Focaccia Crumbles: 400 lb. Gaylord Tote Item # 78939 Sugar Foods Corporation 6190 E. Slauson Ave. Los Angeles, CA 90047
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Drugs)·D-1023-2018·2018-08-08

    Pfizer Recalls Daptomycin Injection Due to Microbial Contamination

    Pfizer is recalling Daptomycin for Injection due to reports of adverse events indicative of infusion reactions related to microbiological contamination.

    Product
    Daptomycin for Injection, 500 mg per vial, packaged as 1 Single-dose vial per carton, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-0106-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2594-2018·2018-08-08

    Integra LifeSciences Recalls Mayfield Infinity XR2 Base Units Due to Fracture Risk

    Integra LifeSciences is recalling Mayfield Infinity XR2 Low Profile Base Units because the knob assembly in the swivel adapter may fracture or break during use.

    Product
    MAYFIELD INFINITY XR2 LOW PROFILE BASE UNIT, Part Number A2079A The MAYFIELD¿ Infinity XR2 Base Unit is intended to be used to support a patient during diagnostic examination and/or surgical procedures where a rigid support between surgical table and headrest, or skull clamp…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2599-2018·2018-08-08

    Beckman Coulter MicroScan Pos Combo Panel Type 43 Recalled for Incorrect Moxifloxacin Dilution

    Beckman Coulter is recalling MicroScan Pos Combo Panel Type 43 because an incorrect Moxifloxacin dilution sequence may cause inaccurate antimicrobial susceptibility results.

    Product
    MicroScan Pos Combo Panel Type 43, Catalog number B1017-217for use in determining antimicrobial agent susceptibility and/or identification to the species level of rapidly growing aerobic and facultative gram-positive cocci, some fastidious aerobic gram-positive cocci and…
    Category
    Medical Device
    Distribution
    12 states
  • SevereNHTSA·18V520000·2018-08-07

    Terex Recalls 2015-2018 Digger Derricks Due to Weld Defect

    Terex is recalling 2015-2018 C4000, C5000, C6000, and General 80 digger derricks because undersized welds may cause the auger to fall unexpectedly, posing an injury risk.

    Product
    TEREX — TEREX C4000, GENERAL 80, C6000, C5000
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V521000·2018-08-07

    BYD Recalls 2016-2017 K11 M Buses Due to Brake Caliper Defect

    BYD is recalling 2016-2017 K11 M hybrid buses because a brake caliper guide pin may break, potentially causing loss of braking ability or tire pressure.

    Product
    BYD — BYD K11 M
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·066-2018·2018-08-03

    Star Natural Meats Recalls Raw Pork Sausage for Undeclared Allergens

    Star Natural Meats is recalling raw pork sausage products because they contain undeclared milk, soy, and restricted ingredients.

    Product
    Star Natural Meats LLC — Star Natural Meats, LLC Recalls Raw Pork Sausage Products due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V513000·2018-08-03

    Mercedes-Benz Recalls 2018 E 400 Cabrio for Child Seat Anchor Defect

    Mercedes-Benz is recalling 2018 E 400 Cabrio vehicles because the child seat anchoring system may not be properly installed, increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E 400
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·18752·2018-08-02

    Rena Ware Recalls Nutrex Pressure Cookers Due to Burn Hazard

    Rena Ware is recalling about 700 Nutrex pressure cookers because they can discharge steam at lower pressures than intended, posing a burn hazard.

    Product
    Nutrex pressure cookers™
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·18186·2018-08-02

    Zebra Thermal Printer Power Supply Units Recalled for Fire Hazard

    Zebra Technologies is expanding a recall of power supply units for thermal printers due to a fire hazard. The units can overheat and catch fire when exposed to moisture.

    Product
    Power supply units for Zebra brand thermal printers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E075000·2018-08-02

    Dexter Trailer Axle Recall for Incorrect Tapered Roller Bearings

    Dexter Axle Company is recalling certain trailer axles because incorrect tapered roller bearings may have been installed, increasing the risk of a crash.

    Product
    SUSPENSION:REAR:AXLE:NON-POWERED AXLE ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V505000·2018-08-02

    Newmar Recalls Motorhomes Due to Brake Caliper Bolt Tightening Issue

    Newmar is recalling 119 motorhomes because brake caliper mounting bolts may be insufficiently tightened, potentially reducing braking performance and increasing crash risk.

    Product
    NEWMAR — NEWMAR VENTANA LE, VENTANA, LONDON AIRE, ESSEX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V508000·2018-08-02

    Subaru Recalls 2019 Ascent Vehicles for Missing B-Pillar Spot Welds

    Subaru is recalling 2019 Ascent vehicles because missing spot welds on the B-Pillar may compromise vehicle strength, increasing the risk of injury in a crash.

    Product
    SUBARU — SUBARU ASCENT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1667-2018·2018-08-01

    Holley Cold Storage Recalls Field Berry Mix Due to Salmonella Risk

    Holley Cold Storage Fruit & Produce Co., Inc. is recalling Europe's Best Field Berry Mix because it may be contaminated with Salmonella.

    Product
    Europe's Best Field Berry Mix 12/600g (Strawberries, Blueberries, Blackberries)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1670-2018·2018-08-01

    Tilgner's Alaskan Salmon Recalls Cold Smoked Sockeye Due to Listeria

    Tilgner's Alaskan Salmon is recalling Ruby Red Sockeye Candy cold smoked salmon in 4 oz packages due to Listeria monocytogenes contamination.

    Product
    Ruby Red Sockeye Candy (ACA) is cold smoked salmon, 4 oz packages
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-1665-2018·2018-08-01

    Holley Cold Storage Recalls Europe's Best 4-Field Berry Mix for Salmonella Risk

    Holley Cold Storage Fruit & Produce Co., Inc. is recalling Europe's Best 4-Field Berry Mix due to potential Salmonella contamination.

    Product
    Europe's Best 4-Field Berry Mix 12/600g and 6/2kg (Blackberries, Strawberries, Blueberries, Raspberries)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1666-2018·2018-08-01

    Holley Cold Storage Recalls Europe's Best Bananas and Berries for Salmonella

    Holley Cold Storage Fruit & Produce Co., Inc. is recalling Europe's Best Bananas & Berries 12/600g in Canada due to potential Salmonella contamination.

    Product
    Europe's Best Bananas & Berries 12/600g (Bananas, Strawberries, Blueberries)
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0981-2018·2018-08-01

    Teva Recalls Valsartan and Hydrochlorothiazide Tablets Due to Carcinogen Impurity

    Teva Pharmaceuticals USA is recalling specific lots of Valsartan and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.

    Product
    Valsartan and Hydrochlorothiazide (HCTZ) Tablets, USP 80 mg/12.5 mg tablets, 90 count-count bottle, Rx Only, Manufactured by: Arrow Pharma (Malta) Ltd. India, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054, NDC 0591-2315-19.
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0971-2018·2018-08-01

    Prinston Recalls Valsartan Tablets Due to Carcinogen Impurity

    Prinston Pharmaceutical Inc. is recalling Valsartan tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.

    Product
    VALSARTAN — VALSARTAN (VALSARTAN)
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0987-2018·2018-08-01

    Teva Recalls Valsartan Tablets Due to Carcinogen Impurity

    Teva Pharmaceuticals USA is recalling specific lots of Valsartan Tablets 80 mg because a carcinogen impurity was detected in the active pharmaceutical ingredient.

    Product
    Valsartan Tablets, USP 80 mg, 90-count bottle (NDC 0591-2168-19), 1000-count bottle (NDC 0591-2168-10), Rx Only, Rx Only, Manufactured by: Arrow Pharma (Malta) Ltd. India, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054
    Category
    Drug
    Distribution
    2 states