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.

22376–22400 of 32171

  • SevereFDA (Food)·F-2966-2015·2015-08-26

    Maruchan Instant Lunch Recalled for Potential Metal Fragments

    Maruchan Inc. is recalling Instant Lunch Con Camaron, Limon y Habanero due to potential metal fragments. The product was distributed only in Mexico and El Salvador.

    Product
    Maruchan Instant Lunch Con Camaron, Limon y Habanero, Contenido Neto 64 g, UPC code: 0 41789 00186 4, Maruchan Inc. Irvine, CA 92618. Product is packaged in a styrofoam cup with cardboard label wrapped around.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2369-2015·2015-08-26

    Teleflex Sheridan SHER-I Bronch Accessory Pack Recalled for Connector Defect

    Teleflex Medical is recalling Sheridan SHER-I Bronch Accessory Packs because the double swivel connector may crack or separate on the endobronchial tube.

    Product
    HUDSON RCI, Sheridan SHER-I BRONCH Accessory Pack, Rx Only, Sterile. Used to aspirate liquids or semisolids from a patient's upper airway.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2985-2015·2015-08-26

    Inventure Foods Recalls Frozen Butter Beans Due to Listeria Risk

    Inventure Foods is recalling specific packages of frozen speckled butter beans due to potential Listeria contamination from GMP violations.

    Product
    Fresh Frozen Grade A Speckled Butter Beans, Net Wt. 32 oz. (2 lb.) 907 g. Dist. By Fresh Frozen Foods, Inc., Jefferson, GA 30549, UPC 0-86069-20000-1; Fresh Frozen Grade A Specked Butter Beans, Net Wt. 80 Oz. (5 lb.) 2268g, Dist. By Fresh Frozen Foods, Inc., Jefferson, GA…
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Drugs)·D-1332-2015·2015-08-26

    Mylan Recalls Gemcitabine Injection Vials Due to Particulate Matter

    Mylan Institutional LLC is recalling specific lots of Gemcitabine for Injection due to the presence of particulate matter. The affected vials were distributed nationwide and in Puerto Rico.

    Product
    Gemcitabine for Injection, USP, 200 mg*/vial, Lyophilized powder in a Single-Use Vial, Rx only, labeled as a) Manufactured for: Mylan Institutional LLC, Rockford, IL 61103, Made in India, NDC 67457-464-20, UPC 3 67457 46420 6; and b) Distributed by Pfizer Labs, Division of…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2967-2015·2015-08-26

    Maruchan Instant Lunch Recalled for Potential Metal Fragments

    Maruchan, Inc. is recalling Instant Lunch Con Camaron due to potential metal fragments. The product was distributed only to Mexico and El Salvador.

    Product
    Maruchan Instant Lunch Con Camaron, Contenido Neto 64 g, UPC code: 0 41789 00195 6, Maruchan Inc. Irvine, CA 92618. Product is packaged in a styrofoam cup with cardboard label wrapped around.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2368-2015·2015-08-26

    Teleflex Recalls Sheridan Sher-I-BRONCH Endobronchial Tubes Due to Connector Cracking

    Teleflex Medical is recalling Sheridan Sher-I-BRONCH endobronchial tubes because the double swivel connector may crack or separate.

    Product
    HUDSON RCI, Sheridan Sher-I-BRONCH, Endobronchial Tube (Right sided), Sizes: 28 Fr., 35 Fr., 37 Fr., 39 Fr. and 41 Fr., Rx Only, Sterile. Intended for use in thoracic surgery, bronchospirometry, for the administration of bronchial anesthesia and other uses commonly requiring…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2433-2015·2015-08-26

    Medline Electrical Surgical Clippers Recalled for Overheating Charging Base

    Medline is recalling 7,602 electrical surgical clippers because the charging base can overheat and smoke. The units were distributed in the U.S. and eight other countries.

    Product
    Medline Electrical Clipper with Charging base The Electrical Surgical Clipper is intended for the removal of body hair from patients as required prior to surgery or other minor procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1349-2015·2015-08-26

    Bausch & Lomb Recalls Bromfenac Ophthalmic Solution Due to Sterility Concerns

    Bausch & Lomb is recalling 13,995 bottles of Bromfenac Ophthalmic Solution, 0.09%, because preservative testing failed, raising concerns about sterility.

    Product
    Bromfenac Ophthalmic Solution, 0.09%, 1.7 mL Bottle, Rx Only. Manufactured by Bausch & Lomb Incorporated Tampa, FL 33637. NDC: 24208-439-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1331-2015·2015-08-26

    Mylan Recalls Carboplatin Injection Due to Particulate Matter

    Mylan Institutional LLC is recalling Carboplatin Injection 450 mg/45 mL due to the presence of particulate matter.

    Product
    CARBOplatin Injection 450 mg/45 mL (10 mg/mL), 45 mL packaged in a 100 mL Multi-Dose Vial, Rx only, Manufactured for: Mylan Institutional LLC, Rockford, IL 61103, Made in India, NDC 67457-493-46, UPC 3 67457 49346 6.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2370-2015·2015-08-26

    Teleflex Medical Recalls Sheridan Double Swivel Connectors Due to Cracking Risk

    Teleflex Medical is recalling Sheridan double swivel connectors because they may crack or separate on endobronchial tubes.

    Product
    HUDSON RCI, Sheridan, SHER-I-SWIV and SHER-I-SWIV/FO Double Swivel, Rx Only, Sterile. Used temporarily to make rigid a flexible tracheal tube to aid its insertion into a patient.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V541000·2015-08-26

    FCA Recalls 2013-2014 Ram Trucks Due to Track Bar Weld Defect

    FCA is recalling 2013-2014 Ram 2500 and 3500 trucks because inadequate welds may cause front track bar brackets to separate, increasing crash risk.

    Product
    RAM — RAM 3500, 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1330-2015·2015-08-26

    PYROLA Advanced Joint Formula Recalled for Undeclared Prescription Drugs

    GC Natural Nutrition is recalling PYROLA Advanced Joint Formula capsules because they contain undeclared prescription and over-the-counter drugs.

    Product
    PYROLA Advanced Joint Formula capsules, 60-count bottle, G & C Natural Nutrition Inc., Fullerton, CA 92833, UPC 7 11746 00075 8.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·15749·2015-08-25

    Cybex Recalls Arm Curl Machines Due to Impact Injury Hazard

    Cybex International is recalling about 4,400 arm curl machines because swivel handles can break off, posing an impact injury hazard to users.

    Product
    Arm Curl Machines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V539000·2015-08-24

    East Manufacturing Recalls 2014-2016 Trailers Due to Wheel Bearing Fire Risk

    East Manufacturing is recalling 2014-2016 trailers because insufficient grease in wheel hubs may cause overheating, leading to fire or wheel detachment.

    Product
    EAST MANUFACTURING — EAST MANUFACTURING FRAME GENESIS TRAILER, DUMP TRAILER, FRAMELESS GENESIS TRAILER, REFUSE TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V538000·2015-08-24

    McNeilus Recalls 2014-2015 CNG Trucks Due to Pressure Relief Defect

    McNeilus is recalling 2014-2015 CNG Refuse and Concrete trucks because pressure relief devices may fail to vent pressure, increasing the risk of tank explosion, fire, and injury.

    Product
    MCNEILUS — MCNEILUS CNG REFUSE TRUCK, CNG CONCRETE TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V535000·2015-08-21

    Strick Van Trailer Recall for Suspension Pivot Bolt Failure Risk

    Strick is recalling 2014 Van Trailers with SAF-Holland suspension systems because pivot bolts may fail, potentially causing the axle to separate from the trailer.

    Product
    STRICK — STRICK VAN TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V532000·2015-08-20

    Oshkosh Recalls 2014-2015 S-Series Concrete Mixers Due to Pressure Relief Defect

    Oshkosh is recalling 2014-2015 S-Series concrete mixers powered by compressed natural gas because pressure relief devices may fail to vent pressure, posing a risk of tank explosion, fire, and injury.

    Product
    OSHKOSH — OSHKOSH S-SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E067000·2015-08-20

    Reyco Granning Recalls Independent Front Suspension Assemblies for Loose Ball Joints

    Reyco Granning is recalling Independent Front Suspension assemblies manufactured between April 2011 and February 2015 due to loose ball joints that could separate and cause a loss of steering control.

    Product
    SUSPENSION:FRONT:CONTROL ARM:LOWER BALL JOINT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2960-2015·2015-08-19

    Patel Grocery Coriander Powder Recalled for Undeclared Peanut Allergen

    Patel Grocery Corp is recalling America's Best Coriander Powder in New York due to undeclared peanut allergens.

    Product
    AMERICA'S BEST CORRIANDER POWDER, NET WT.: 1) 7 OZ, 2) 14 OZ. (400 GMS) and 3) 28 OZ, sealed in plastic bags, Packed by Patel Grocery 5303 4th Ave. Brooklyn, NY 11220
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2358-2015·2015-08-19

    Invacare Pronto Air Power Wheelchair Recall for Battery Overheating Risk

    Invacare is recalling 1,057 Pronto Air power wheelchairs because the batteries may overheat during charging, posing risks of chemical burns and property damage.

    Product
    Invacare¿ Pronto¿ Air Personal Transporter (power wheelchair), Invacare Corporation, One Invacare Way, Elyria, Ohio, 44035-4190, (800) 333 -6900.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2323-2015·2015-08-19

    Alcon ReSTOR Intraocular Lenses Recalled for Post-Operative Inflammation Reports

    Alcon Research, Ltd. is recalling ReSTOR intraocular lenses manufactured for Japan due to reports of post-operative inflammation and toxic anterior segment syndrome (TASS). No US distribution occurred.

    Product
    ReSTOR intraocular lens and ReSTOR Toric intraocular lens. The Alcon AcrySof IQ ReSTOR and IQ ReSTOR Toric intraocular lenses are posterior chamber lenses intended as optical implants designed to replace the human crystalline lens in adult patients following cataract surgery.…
    Category
    Medical Device
    Distribution
    0 states