The Recall Desk

Severity 4 of 5

Severe recalls

The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.

What “severe” means here

Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

23626–23650 of 32184

  • SevereNHTSA·15V176000·2015-03-25

    Yamaha Recalls 2015 Motorcycles Due to Transmission Shift Cam Defect

    Yamaha is recalling 4,900 model year 2015 motorcycles because a defective shift cam stopper may fracture, causing transmission shifting issues and increasing crash risk.

    Product
    YAMAHA — YAMAHA SUPER TENERE ES, FZ-09, SUPER TENERE, FZ6R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0416-2015·2015-03-25

    Heritage Pharmaceuticals Recalls RIFAMPIN for Injection Due to Sterility Concerns

    Heritage Pharmaceuticals is recalling RIFAMPIN for Injection, USP, 600 mg per vial, due to quality control concerns regarding the assurance of sterility.

    Product
    RIFAMPIN for Injection,USP, 600 mg per vial, Rx Only, Manufactured by: Emcure Pharmaceuticals Ltd., Hinjwadi, Pune, India Manufactured for: Heritage Pharmaceuticals Inc., Eatontown, NJ 07724 NDC 23155-340-31
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1419-2015·2015-03-25

    Twin City Bagel Recalls Cinnamon Raisin Bagels for Undeclared Peanuts or Almonds

    Twin City Bagel, Inc. is recalling specific Cinnamon Raisin bagels because they may contain undeclared peanuts or almonds.

    Product
    Cinnamon Raisin bagels sold under the following brands and sizes: 1. Dan's Pantry 6 count, UPC 76057-00479 2. Essential Everyday 5 count, Keep Refrigerated, UPC 41303-00678 3. Jewel 6 count, UPC 4128001267 4. L'Oven Fresh 6 count, UPC 41498-19170 5. Pepperidge Farm, 21…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1417-2015·2015-03-25

    Twin City Bagel Recalls Plain Bagels for Undeclared Peanuts or Almonds

    Twin City Bagel, Inc. is recalling plain bagels sold under multiple brand names because they may contain undeclared peanuts or almonds.

    Product
    Plain Bagels sold under the follow brand names and sizes: 1. Dan's Pantry Bagels 6 count, UPC 76057-00479, 2. Essential Everyday 5 count, Keep Refrigerated, UPC 41303-00683 3. Jewel 6 count, UPC 41280-01268, 4. Kroger 6 count, UPC 11110-02884 5. Kroger Mini 12 count, UPC…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1288-2015·2015-03-25

    Ossur LP Rotate Foot System Recalled for Insecure Assembly

    Ossur H / F is recalling LP Rotate Foot System prosthetic devices because short threads on the shock module may cause it to detach, leading to falls.

    Product
    LP Rotate Foot System prosthetic device for fitting lower extremity amputations. -Low profile foot module with adjustable shock absorber and rotation with progressive stiffening -Build height: with male pyramid adapter 145 - 153mm (5 11/16 - 6 ) with female pyramid…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1418-2015·2015-03-25

    Twin City Bagel Recalls Whole Wheat Bagels for Undeclared Peanuts or Almonds

    Twin City Bagel, Inc. is recalling specific brands of whole wheat bagels because they may contain undeclared peanuts or almonds.

    Product
    Whole Wheat bagels sold under the following brands and sizes: 1. Kroger 6 count, UPC 11110-02887 2. Lender's 6 count, UPC 76800-56333 3. L'Oven Fresh Mini 12 count, UPC 41498-17880 4. Pepperidge Farm Mini 17 oz., UPC 14100084938 5. Thomas' 6 count, UPC 4812125505 6.…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1276-2015·2015-03-25

    Medtronic FlexCath Select Steerable Sheath Recalled for Valve Debris

    Medtronic is recalling 151 FlexCath Select Steerable Sheaths because clinicians observed debris originating from the hemostasis valve outside of patients' bodies.

    Product
    Medtronic, 10 Fr FlexCath Select Steerable Sheath 990065. The FlexCath Select Steerable Sheath (10 Fr Select) is used for percutaneous catheter introduction into the vasculature and chambers of the heart. The sheath is a single-use device and is not implantable.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1424-2015·2015-03-25

    Kroger Cinnamon Swirl Raisin Bagels Recalled for Undeclared Peanuts or Almonds

    Twin City Bagel, Inc. is recalling Kroger Cinnamon Swirl Raisin Bagels because they may contain undeclared peanuts or almonds.

    Product
    Kroger Cinnamon Swirl Raisin Bagels, 6 count, UPC 11110-02885, and 12 count Mini UPC UPC 11110-02890
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1435-2015·2015-03-25

    Jack and the Beanstalk Soybean Sprouts Recalled for Listeria

    Jack and the Beanstalk soybean and natto sprouts are being recalled in California due to positive FDA sampling for Listeria monocytogenes.

    Product
    Jack and the Beanstalk Soybean Sprouts and Natto Sprouts; Packaged in 1 lb., 1.5 lb. and 10 lb. packages. and Natto Soybean sprouts packed in 396 g. plastic bags
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1428-2015·2015-03-25

    Aron Streit Recalls Dark Chocolate Coins for Undeclared Milk

    Aron Streit Inc. is recalling Streit's Kids Dark Chocolate Coins because testing revealed undeclared milk, a major allergen.

    Product
    Streit's Kids Dark CHOCOLATE Coins, 24 x 0.5 oz (15g) mesh bags. UPC 70227 50121. PRODUCT OF TURKEY IMPORTED & DISTRIBUTED BY ARON STREIT INC. NEW YORK, NY 10002 USA.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0414-2015·2015-03-25

    Mutual Pharmaceutical Recalls Ergoloid Mesylates Tablets Due to Impurities

    Mutual Pharmaceutical is recalling Ergoloid Mesylates 1 mg tablets because they failed impurity and degradation specifications during stability testing.

    Product
    Ergoloid Mesylates ,1 mg tablets, 100 count bottle, Rx only, Manufactured by MUTUAL PHARMACEUTICAL CO., INC., PHILADELPHIA, PA 19124 USA for Sun Pharmaceutical Industries, Inc. 270 Prospect Plains Road, Cranbury, NJ 08512. NDC 53489-281-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0417-2015·2015-03-25

    Hospira Recalls 5% Dextrose Injection Due to Sterility Concerns

    Hospira is recalling 94,440 bags of 5% Dextrose Injection due to a potential leak at the administrative port that compromises sterility.

    Product
    DEXTROSE — DEXTROSE (DEXTROSE MONOHYDRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V172000·2015-03-24

    Ford Recalls 2013-2015 Lincoln MKT Vehicles Due to Fire Risk

    Ford is recalling specific 2013-2015 Lincoln MKT vehicles with limousine or hearse packages because a vacuum pump relay may overheat, increasing the risk of a vehicle fire.

    Product
    LINCOLN — LINCOLN MKT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V170000·2015-03-24

    Spartan Recalls 2011-2016 School Bus Chassis Due to Fire Risk

    Spartan Motors is recalling 2011-2016 school bus chassis because fuel system components may melt, causing engine stalls or vehicle fires.

    Product
    SPARTAN — SPARTAN SB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V165000·2015-03-23

    Navistar Recalls 2015-2016 International Trucks Due to Brake Fire Risk

    Navistar is recalling 2015-2016 International and IC Bus vehicles because defective brake actuators may cause dragging, overheating, and wheel end fires.

    Product
    INTERNATIONAL — INTERNATIONAL, IC BUS TRANSTAR, CE, DURASTAR, WORKSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V168000·2015-03-23

    Navistar Recalls 2015 IC RE Transit Buses for Brake Hose Defect

    Navistar is recalling 2015 IC RE non-school Transit Buses because the front air brake hose may contact the tire, causing leaks and increased crash risk.

    Product
    IC BUS — IC BUS RECB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V166000·2015-03-23

    Navistar Recalls 2015-2016 IC School Buses for Brake Fire Risk

    Navistar is recalling specific 2015-2016 IC school buses because defective air brake actuators may cause dragging brakes and wheel end fires.

    Product
    IC BUS — IC BUS CASB, CESB, RESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V159000·2015-03-20

    Charles Machine Recalls Ditch Witch T26 Trailers Due to Bearing Defect

    Charles Machine is recalling 2002-2015 Ditch Witch T26 trailers because incorrect wheel bearings may fail, causing the wheel to detach and increasing crash risk.

    Product
    CHARLES MACHINE — CHARLES MACHINE DITCH WITCH T26
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·050-2015·2015-03-20

    Boa Vida Imports Recalls Pork and Beef Products from Portugal

    Boa Vida Imports is recalling pork and beef products imported from Portugal without inspection because the country is ineligible to export meat to the U.S.

    Product
    Boa Vida Imports Recalls Pork And Beef Products Imported From An Ineligible Country Without Benefit Of Import Inspection
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·15V160000·2015-03-20

    Forest River Recalls 2013-2014 Sabre Trailers Due to Brake Wiring Defect

    Forest River is recalling 2013-2014 Sabre travel trailers and fifth wheels because improperly routed brake wires may chafe, break, or short, increasing crash and fire risks.

    Product
    FOREST RIVER — FOREST RIVER SABRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1251-2015·2015-03-18

    Philips DuraDiagnost X-Ray System Recalled for Installation Defects

    Philips Medical Systems is recalling 71 DuraDiagnost X-Ray systems worldwide due to improper installation risks that could cause equipment to fall or float.

    Product
    Philips DuraDiagnost X-Ray system, Stationary X-Ray System Radiographic Models: 712210, 712211
    Category
    Medical Device
    Distribution
    0 states