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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17251–17275 of 39601

  • SevereFDA (Drugs)·D-1175-2018·2018-09-12

    AvKARE Valsartan and Hydrochlorothiazide Tablets Recalled for Carcinogen Impurity

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

    Product
    AvKARE Valsartan and Hydrochlorothiazide 160 mg/25 mg tablets, 90-count bottle, Rx Only, Manufactured for: AvKARE, Inc. Pulaski, TN 38478, NDC 42291-887-90
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2962-2018·2018-09-12

    Bayer Medical Care Recalls Overhead Counterpoise Systems Due to Structural Risk

    Bayer Medical Care is recalling four Overhead Counterpoise Systems because overtightened bolts may compromise structural integrity, posing a risk of injury.

    Product
    Overhead Counterpoise Systems (OCS), OCS, 580mm CEILING MOUNT, PORTEGRA2, Catalog # OCS CEIL 58, Material Number 84433765
    Category
    Medical Device
    Distribution
    3 states
  • SevereFDA (Devices)·Z-2961-2018·2018-09-12

    Bayer Overhead Counterpoise Systems Recalled for Potential Structural Failure

    Bayer Medical Care is recalling one Overhead Counterpoise System unit due to potential overtightening of bolts that could compromise structural integrity.

    Product
    Overhead Counterpoise Systems (OCS) OCS CONF an accessory device for use with Bayer injector systems as a support for an injector head. , SHORT CEIL MNT, STD HORZ ARM, Catalog # OCS 115AS, Material Number 59880288
    Category
    Medical Device
    Distribution
    3 states
  • SevereUSDA FSIS·079-2018·2018-09-12

    Roya Foods Recalls Raw Halal Manti Beef Dumplings Produced Without Inspection

    Roya Foods is recalling approximately 438 pounds of raw Halal Manti Beef Dumplings because they were produced without federal inspection. No adverse reactions have been reported.

    Product
    Roya Foods, LLC Recalls Halal Manti Beef Dumpling Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·18V616000·2018-09-12

    Highland Ridge RV Recalls 2019 Travel Trailers Due to Axle Bearing Defect

    Highland Ridge RV is recalling 2019 Open Range and Mesa Ridge travel trailers because missing inner bearing races may cause hub failure and increase crash risk.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT OPEN RANGE ULTRA LITE, OPEN RANGE LITE, MESA RIDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1172-2018·2018-09-12

    McKesson Recalls Megestrol Acetate Oral Suspension Due to Supra-Potent Drug

    McKesson is recalling 1,531 cartons of Megestrol Acetate Oral Suspension because the drug is supra-potent. The recall is voluntary and nationwide.

    Product
    Megestrol Acetate Oral Suspension, USP 400 mg/mL, 10 mL (10 mL UD cups in boxes of 20 cups), Rx Only, Mfg. By: Par Pharmaceutical One Ram Ridge Rd Chestnut Ridge, NY 10977 Dist. By: McKesson Packaging Services a business unit of McKesson Corporation 7101 Weddington Rd. Concord…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1946-2018·2018-09-12

    Fresh Express Recalls Chopped Romaine Due to Cyclospora Test Result

    Fresh Express is recalling 482 cases of Chopped Romaine 1 lb after a test detected the Cyclospora organism. The product was distributed in 15 U.S. states.

    Product
    Fresh Express Chopped Romaine 1 lb
    Category
    Food
    Distribution
    15 states
  • SevereFDA (Devices)·Z-2960-2018·2018-09-12

    Bayer Overhead Counterpoise Systems Recalled for Potential Structural Failure

    Bayer Medical Care is recalling two Overhead Counterpoise Systems because overtightened bolts may compromise structural integrity, posing a risk of injury.

    Product
    Overhead Counterpoise Systems (OCS), OCS CONF,STD CEIL MNT, STD HORZ ARM, Catalog # OCS 115A, Material Number 59880253
    Category
    Medical Device
    Distribution
    3 states
  • SevereNHTSA·18V618000·2018-09-12

    Jayco Recalls 2019 Travel Trailers Due to Missing Axle Bearing Races

    Jayco is recalling 2019 White Hawk, Jay Flight, and Jay Flight SLX travel trailers because missing inner bearing races may cause hub overheating and axle separation.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER JAY FLIGHT SLX, JAY FLIGHT, WHITE HAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·078-2018·2018-09-11

    CTI Foods Recalls Ready-to-Eat Philly Beef Steak for Listeria Risk

    CTI Foods LLC is recalling approximately 6,720 pounds of ready-to-eat Philly Beef Steak products due to possible Listeria monocytogenes contamination.

    Product
    CTI Foods LLC. — CTI Foods LLC Recalls Ready-To-Eat Philly Steak Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·18V612000·2018-09-11

    Ford Recalls 2018 Edge and Lincoln MKX for Door Striker Bolt Defect

    Ford is recalling 2018 Ford Edge and Lincoln MKX vehicles because shorter-than-intended door striker bolts may cause doors to open in a crash, increasing injury risk.

    Product
    FORD — FORD, LINCOLN EDGE, MKX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V608000·2018-09-11

    Mercedes-Benz Recalls 2018 C-Class Models Due to Rear Window Bonding Defect

    Mercedes-Benz is recalling 2018 C300, C300 4MATIC, C63 AMG, and C63S AMG vehicles because incorrect rear window bonding may cause the glass to detach, creating a road hazard.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES BENZ AMG C63S, C 300 4MATIC, C 300, AMG C63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V585000·2018-09-08

    Trailstar Recalls 2019 Dump Trailers Due to Wheel Separation Risk

    Trailstar is recalling 2019 Dump trailers because improperly installed wheel end nuts may cause the wheel to separate from the axle, increasing crash risk.

    Product
    TRAILSTAR — TRAILSTAR DUMP TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V595000·2018-09-07

    GM Recalls 2014-2016 Cadillac CTS for Seat Heater Fire Risk

    General Motors is recalling 2014-2016 Cadillac CTS vehicles because damaged front seat heaters may overheat and cause a fire when the car is remotely started.

    Product
    CADILLAC — CADILLAC CTS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V598000·2018-09-07

    Navistar Recalls 2019 IC Bus School Buses Due to Brake Defect

    Navistar is recalling 2019 IC Bus CE and RE school buses because a parking brake component may be improperly crimped, causing air leaks and increased stopping distances.

    Product
    IC BUS — IC BUS CESB, RESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V597000·2018-09-07

    Navistar Recalls 2019 International and IC Bus Vehicles for Brake Defect

    Navistar is recalling 2,089 2019 International and IC Bus vehicles because a brake chamber defect may cause air leaks, increasing stopping distance and crash risk.

    Product
    INTERNATIONAL — INTERNATIONAL, IC BUS LT, HX, WORKSTAR, DURASTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V599000·2018-09-07

    Honda Recalls 2017 Acura NSX for Brake Light Circuit Defect

    Honda is recalling 793 2017 Acura NSX vehicles because road vibrations may loosen screws, causing the center brake light to fail and increasing crash risk.

    Product
    ACURA — ACURA NSX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V601000·2018-09-07

    Nissan Recalls Murano, Maxima, Pathfinder, and QX60 for Brake Fire Risk

    Nissan is recalling specific 2015-2018 Murano, Maxima, Pathfinder, and 2017 QX60 vehicles because brake fluid leaks may cause electrical shorts and fires.

    Product
    NISSAN — NISSAN, INFINITI MURANO, QX60, MAXIMA, PATHFINDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0004-2019·2018-09-05

    Living Well Remedies Weight Away Remedy Recalled for Microbial Contamination

    Living Well Remedies is recalling Weight Away Remedy spray bottles due to out-of-specification microbial results.

    Product
    Living Well Remedies Weight Away Remedy, 2 fl oz (59 mL) Distributed by Living Well Remedies, LLC P.O. Box 704, Franklin Lakes, NJ 07417 www.LivingWellRemedies.com. Made in the USA
    Category
    Drug
    Distribution
    0 states
  • CriticalFDA (Food)·F-1853-2018·2018-09-05

    Marsee Foods Recalls Cafe YUMM! Ginger Spice Cookies for Undeclared Peanuts

    Marsee Foods Inc is recalling Cafe YUMM! Ginger Spice Cookies because they may contain undeclared peanuts. The affected cookies were sold in Oregon and Washington.

    Product
    Ginger Spice Cookies, brand Cafe YUMM! Product is packaged in shrink wrapped master case. Each master case contains two boxes and each box contains 24 cookies. The master case is taped shut and labeled with the contents and production date, along with a lot code. The…
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-1854-2018·2018-09-05

    Marsee Foods Recalls Oatmeal Raisin Cookies for Undeclared Peanuts

    Marsee Foods is recalling Oatmeal Raisin Cookies sold at Cafe YUMM! restaurants in Oregon and Washington because they may contain undeclared peanuts.

    Product
    Oatmeal Raisin Cookies, brand Cafe YUMM! Product is packaged in shrink wrapped master case. Each master case contains two boxes and each box contains 24 cookies. The master case is taped shut and labeled with the contents and production date, along with a lot code. The…
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-1162-2018·2018-09-05

    Auro Pharmacies Recalls Methyl-Cobalamin Injectable Due to Sterility Concerns

    Auro Pharmacies is recalling 81 vials of Methyl-Cobalamin injectable because processes and equipment were inadequate to assure sterility.

    Product
    Methyl-Cobalamin injectable, 10 mg/mL, 30 mL Multiple Dose vial, Rx only, Central Drugs Compounding Pharmacy, 520 W. La Habra Blvd, La Habra, CA 90631
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2951-2018·2018-09-05

    Haemonetics OrthoPAT Reservoirs Recalled Due to Missing Cannula

    Haemonetics is recalling 348 OrthoPAT QuickConnect Reservoirs because a missing cannula prevents blood from being emptied and processed.

    Product
    Haemonetics¿ OrthoPAT¿ System-OPAT QuickConnect Reservoirs. Product Code: OPT-R-1000 The OrthoPAT orthopedic perioperative autotransfusion system indicated for use to salvage RBCs from blood lost intraoperatively and postoperatively during surgical procedures
    Category
    Medical Device
    Distribution
    Distributed nationwide