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.

Filters

Agency

Category

Minimum severity

Clear filters

34976–35000 of 39756

  • SevereFDA (Drugs)·D-272-2013·2013-05-01

    Sodium Tetradecyl Sulfate Injectable Recalled for Sterility Assurance Concerns

    Axium Healthcare Pharmacy is recalling Sodium Tetradecyl Sulfate Injectable due to lack of sterility assurance and quality control concerns.

    Product
    Sodium Tetradecyl Sulfate Injectable Balanced Solutions, Compounding Pharmacy a division of Axium Healthcare Pharmacy, Inc., Lake Mary, FL 32746
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-288-2013·2013-05-01

    Axium Healthcare Recalls DMSO Bladder Irrigation Solution Due to Sterility Concerns

    Axium Healthcare Pharmacy is recalling DMSO 50% Sterile Bladder Irrigation Solution because the company cannot ensure the product is sterile.

    Product
    DMSO 50% Sterile Bladder Irrigation Solution Injectable Balanced Solutions, Compounding Pharmacy a division of Axium Healthcare Pharmacy, Inc., Lake Mary, FL 32746
    Category
    Drug
    Distribution
    4 states
  • SevereNHTSA·13V165000·2013-04-30

    Westmor Trailer Recall for Defective Pressure Relief Valves

    Westmor is recalling 2003-2013 trailers with specific Fisher pressure relief valves that may break and eject, posing injury and fire risks.

    Product
    WESTMOR — WESTMOR TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13E022000·2013-04-30

    Prevost Recalls Parking Brake Chambers Due to Fire Risk

    Prevost is recalling 416 parking brake chambers that may leak air, causing brakes to drag and overheat, which could result in a fire.

    Product
    PARKING BRAKE:CONVENTIONAL:AIR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V166000·2013-04-29

    Mercedes-Benz Recalls 2013 GL Models for Seat Belt Anchor Bolt Defect

    Mercedes-Benz is recalling 2013 GL350, GL450, GL550, and GL63 vehicles because second-row seat belt anchor bolts may not be properly torqued, increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GL63, GL350, GL450, GL550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V167000·2013-04-25

    HME Recalls 2011-2012 Fire Apparatus Due to Brake Dragging Risk

    HME is recalling 11 fire apparatus vehicles because parking brake chambers may leak, causing brakes to drag and overheat, which could result in a fire.

    Product
    HME — HME, FERRARA SPECTR FIRE APPARATUS, SPECTR, INTRUDER EMBER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V190000·2013-04-25

    Setra Recalls S417 TC and S407 Motorcoaches Due to Fire Risk

    Setra is recalling 2011-2013 S417 TC and 2012-2013 S407 motorcoaches because moisture in the engine compartment can cause electrical corrosion and potential fire.

    Product
    SETRA — SETRA S417 TC, S407
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1315-2013·2013-04-24

    Publix Deli Tri Fruit and Grain Salad Recalled for Listeria Risk

    Publix Super Markets is recalling specific 12oz containers of Deli Tri Fruit and Grain Salad because the product may be adulterated with Listeria monocytogenes.

    Product
    Publix Deli Tri Fruit and Grain Salad with red rice, red wheat, quinoa, apricots, cranberry and raisins 12oz. In a clear plastic container.
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Drugs)·D-263-2013·2013-04-24

    Hospira Recalls Lactated Ringer's Injection Due to Non-Sterility

    Hospira is recalling Lactated Ringer's and 5% Dextrose Injection due to a confirmed report of non-sterility involving spore-like particulates consistent with mold.

    Product
    Lactated Ringer's and 5% Dextrose Injection, USP, 1000 mL flexible containers, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7929-09.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1316-2013·2013-04-24

    Little Mermaid Smoked Herring Recalled for Botulism Risk

    Little Mermaid Smokehouse is recalling smoked herring found to be uneviscerated during an FDA inspection due to the potential for Clostridium botulinum.

    Product
    Little Mermaid Brand Smoked Herring.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Drugs)·D-265-2013·2013-04-24

    Body Basics Recalls Actra-SX Capsules Containing Unapproved Sildenafil

    Body Basics Inc is recalling Actra-SX 500 capsules because they contain sildenafil, an active ingredient in FDA-approved erectile dysfunction drugs, without an approved NDA or ANDA.

    Product
    Actra-SX 500 Capsules, Maximum Strength, Energizer, 500 mg, 5 count package, Body Basics, Canoga Park, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1317-2013·2013-04-24

    Little Mermaid Pickled Herring Recalled for Potential Botulism Risk

    Little Mermaid Smokehouse is recalling pickled herring found to be uneviscerated during an FDA inspection due to the potential for Clostridium botulinum.

    Product
    Little Mermaid Brand Pickled Herring.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Drugs)·D-266-2013·2013-04-24

    FDA Recalls Blue Male Enhancement Pill for Unapproved Ingredient

    The Menz Club is recalling Blue Male Enhancement Pill because it contains sulfoaildenafil, an unapproved analogue of sildenafil.

    Product
    Blue Male Enhancement Pill, bulk product, by The Menz Club, Ridgeland, MS
    Category
    Drug
    Distribution
    1 state
  • CriticalFDA (Drugs)·D-262-2013·2013-04-24

    Hospira Recalls Lactated Ringer's Injection Due to Mold Contamination

    Hospira is recalling 143,136 units of Lactated Ringer's and 5% Dextrose Injection due to confirmed mold contamination.

    Product
    Lactated Ringer's and 5% Dextrose Injection, USP, 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA; NDC 0409-7929-09.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1116-2013·2013-04-24

    Hospira GemStar Infusion Pump Recall for Potential Over-Infusion Risk

    Hospira is recalling GemStar infusion pumps because the motor may rotate backwards during low-rate infusions, potentially causing over-infusion of medication.

    Product
    The GemStar Pump is a small and lightweight, single channel infusion device designed for use in the home, in the hospital, or anywhere electronic infusion is required. The GemStar Pump can be powered by AC mains adaptor, rechargeable battery pack, docking station, or two…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1052-2013·2013-04-24

    Stryker Recalls ShapeMatch Cutting Guides Due to Internal Process Issues

    Stryker Orthopaedics is recalling ShapeMatch Cutting Guides used in knee surgeries due to potential issues with internal planning and production processes.

    Product
    ShapeMatch Cutting Guides Product Usage: The ShapeMatch Cutting Guides are intended to be used as patient-specific surgical instrumentation to assist in the positioning of total knee arthroplasty components intraoperatively and in guiding the marking of bone before cutting.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1150-2013·2013-04-24

    Advanced Sterilization Products Recalls EVOTECH Endoscope Cleaner Due to Smoke Risk

    Advanced Sterilization Products is recalling 761 EVOTECH Endoscope Cleaner and Reprocessor systems because a circuit board malfunction can cause smoke to emanate from the device.

    Product
    EVOTECH Endoscope Cleaner and Reprocessor System, P/N 50004. Designed to automatically clean and high-level disinfect flexible, submersible video or fiber-optic endoscopes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V161000·2013-04-24

    Winnebago and Itasca Motorhomes Recalled for Missing Range Enclosure

    Winnebago is recalling 2012-2014 motorhomes because a missing range enclosure may allow propane gas to flow without a flame, creating a fire hazard.

    Product
    ITASCA — ITASCA, WINNEBAGO CAMBRIA, MINNIE WINNIE, MERIDIAN, SUNCRUISER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1098-2013·2013-04-24

    Carefusion Recalls Alaris PC Units Due to Communication Errors

    Carefusion is recalling Alaris PC unit model 8015 with software version 9.12 due to communication errors when specific monitoring modules are attached.

    Product
    Alaris PC unit model 8015 with software version 9.12 Product Usage: The Alaris PC unit is the central programming, monitoring and power supply component for the Alaris System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1126-2013·2013-04-24

    Accuray CyberKnife Iris Variable Aperture Collimator Recall for Beam Axis Shift

    Accuray Incorporated is recalling 176 Iris Variable Aperture Collimators for the CyberKnife System due to a defect that could shift the radiation beam's central axis.

    Product
    Accuray CyberKnife System Medical Physicist, Robotic Radiosurgery System, Medical charged-particle radiation therapy system, Model: Iris Variable Aperture Collimator P/Ns 028986 and 031777. The CyberKnife System is indicated for radiation treatment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1128-2013·2013-04-24

    SR Instruments FG3105 Patient Scales Recalled Due to Load Cell Failures

    SR Instruments is recalling 806 FG3105 patient scales used with Joerns Healthcare lifters after two load cell failures caused patient falls.

    Product
    SR Instruments FG3105 Patient Scales Used on various Joerns Healthcare Patient Lifters. Model# FG3105 Patient Scales. Product Usage: The FG3105 Scale is designed for Joerns Healthcare for use in portable patient weighing systems. The scale is designed to be connected…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-249-2013·2013-04-24

    Teva Recalls Copaxone Syringes Due to Visible Silicone Oil Presence

    Teva Pharmaceuticals is recalling 6,692 boxes of Copaxone (glatiramer acetate) injection due to visible medical grade silicone oil in the syringes.

    Product
    COPAXONE — COPAXONE (GLATIRAMER ACETATE)
    Category
    Drug
    Distribution
    Distributed nationwide