The Recall Desk

Archive

February 2015 recalls

651 recalls were announced in February 2015.

What the numbers show

Critical
223
Severe
214
High
145
Moderate
59
Low
10

Of the 651 recalls this month scored against our rubric, 34% are Critical, 33% are Severe.

Which agencies issued them

401–500 of 651

  • SevereFDA (Food)·F-1015-2015·2015-02-11

    Husky Spumoni Ice Cream Recalled for Potential Listeria Contamination

    Husky Ice Cream is recalling Spumoni ice cream due to potential Listeria monocytogenes contamination from a recalled ingredient.

    Product
    Spumoni ice cream is packed in 2.5 gallon bulk, 1.5 gallon bulk, or half gallon retail size tubs. Retail size ice cream flavor is labeled in part, "***Husky Ice Cream, Inc. 4721 California Ave SW Seattle, WA 98116 HUSKY "Cream of the Town" HALF GALLON ICE CREAM…
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0382-2015·2015-02-11

    Hospira Recalls Lidocaine Hydrochloride Injection Due to Particulate Matter

    Hospira Inc. is recalling 120,900 vials of 1% Lidocaine Hydrochloride Injection because iron oxide particulates were found in the solution.

    Product
    LIDOCAINE HYDROCHLORIDE — LIDOCAINE HYDROCHLORIDE (LIDOCAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1036-2015·2015-02-11

    Invacare Recalls G-Series Bed Rails Due to Entrapment Safety Defect

    Invacare is recalling G-Series bed rails because the mounting bracket does not meet entrapment safety specifications.

    Product
    G- Series Beds; G29 full length bed rails assembly
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1042-2015·2015-02-11

    Zimmer Persona Tibial Inserter Recalled for Potential Tip Fracture

    Zimmer, Inc. is recalling 1,091 Persona Tibial Articular Surface Inserters due to a potential fracture of the instrument tip, which could cause tissue damage or require revision surgery.

    Product
    Zimmer PERSONA Tibial Articular Surface Inserter; Item # 42-5299-001-00. Manual surgical instrument for knee arthroplasty (orthopedic).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0977-2015·2015-02-11

    Riba Foods Recalls Salpica Ballpark Nachos Due to Undeclared Wheat

    Riba Foods Inc is recalling Salpica 8 oz. Ballpark Nachos because the product may contain undeclared wheat. The recall affects 6,564 units distributed across 23 states.

    Product
    Salpica 8 oz. Ballpark Nacho; 6 units per case
    Category
    Food
    Distribution
    23 states
  • HighFDA (Food)·F-0976-2015·2015-02-11

    Riba Foods Recalls Salpica Salsa Con Queso for Undeclared Wheat

    Riba Foods Inc is recalling Salpica Salsa Con Queso because the product may contain undeclared wheat. This poses a risk to individuals with wheat allergies or celiac disease.

    Product
    Salpica 11.5 oz., 16 oz., Salsa Con Queso; 12 units per case
    Category
    Food
    Distribution
    23 states
  • HighCPSC·15077·2015-02-11

    System Sensor Recalls Combination Carbon Monoxide and Smoke Detectors

    System Sensor is recalling i4 Series combination CO/smoke detectors because they may fail to detect carbon monoxide, posing a poisoning risk.

    Product
    i4 Series System Sensor combination carbon monoxide (CO)/smoke detectors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1038-2015·2015-02-11

    SCC Soft Computer Recalls SoftLab Laboratory Information System Versions

    SCC Soft Computer is recalling SoftLab versions 4.0.7.0 and 4.0.7.1 because the software fails to send abnormal flags for Reference Lab test results.

    Product
    SoftLab with SA HIS versions 4.0.7.0-4.0.7.1 SoftLab is a laboratory information system to be used in a medical research or clinical laboratory.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0972-2015·2015-02-11

    Zilks Foods Recalls Green Chili Hummus Due to Undeclared Peanuts

    Zilks Foods is recalling 3,176 cups of Green Chili Hummus because the cumin ingredient may contain undeclared peanuts.

    Product
    Hummus; All-natural ZILKS HATCH GREEN CHILI HUMMUS GLUTEN FREE & NON-GMO NET WT. 8 OZ
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0971-2015·2015-02-11

    Zilks Foods Recalls Balsamic and Garlic Hummus for Undeclared Peanuts

    Zilks Foods is recalling 2,424 cups of Balsamic and Garlic Hummus due to potential undeclared peanuts in the cumin ingredient.

    Product
    Hummus; All-natural ZILKS BALSAMIC & GARLIC HUMMUS GLUTEN FREE & NON-GMO NET WT. 8 OZ
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0973-2015·2015-02-11

    Zilks Spinach and Artichoke Hummus Recalled for Undeclared Peanuts

    Zilks Foods is recalling Spinach & Artichoke Hummus because the cumin ingredient may contain undeclared peanuts.

    Product
    Hummus; All-natural ZILKS SPINACH & ARTICHOKE HUMMUS GLUTEN FREE & NON-GMO NET WT. 8 OZ
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1049-2015·2015-02-11

    Carl Zeiss Meditec FORUM Archive and Viewer Software Recall

    Carl Zeiss Meditec is recalling FORUM Archive and Viewer software versions 3.1 and 3.2 due to a defect that may lead to misinterpretation of optical coherence tomography data.

    Product
    FORUM Archive and Viewer, version 3.1, v 3.1.1, (DVD Format) and v 3.2, v 3.2.1.(DVD and USB Flash Drive Format). Catalog numbers: 000000-20107-750 (DVD with either FORUM v 3.1 or v 3.1.1) 000000-2058-601 (DVD with either FORUM v 3.2 or 3.2.1); 000000-2084-928 (USB drive…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1060-2015·2015-02-11

    Shape Medical Systems Recalls Cardiopulmonary Testing System Patient Interfaces

    Shape Medical Systems is recalling 564 disposable patient interfaces for the Shape-HF Cardiopulmonary Testing System because they may produce erroneous results, potentially leading to incorrect diagnosis and treatment.

    Product
    Shape-HF Cardiopulmonary Testing System Disposable Patient Interface (DPI). Part Number 0004-4001. The Shape-HF Cardiopulmonary Exercise Testing System is a stationary device that monitors parameters during laboratory or clinical conditions.
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Devices)·Z-1039-2015·2015-02-11

    Baxter Integrated APD Set Recalled for Leakage Complaints

    Baxter Healthcare is recalling 8,640 units of Integrated APD Sets with Cassette 3-Prong due to leakage complaints. The sterile fluid path is used for peritoneal dialysis.

    Product
    Baxter Integrated APD Set with Cassette 3-Prong, Sterile, nonpyrogenic fluid path. Product Usage: The recall device is indicated for use in the treatment of patients with renal failure to provide PD fluid exchanges with Baxter HomeChoice PD Systems in clinical and home use…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1040-2015·2015-02-11

    Sedecal MobileDiagnost wDR X-ray systems recalled for unexpected movement

    Sedecal S.A. is recalling 283 MobileDiagnost wDR motorized portable diagnostic X-ray systems due to reports of unexpected movement.

    Product
    MobileDiagnost wDR motorized portable diagnostic X-ray systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1046-2015·2015-02-11

    Radiometer ABL90 FLEX Analyzer Recall for Calibration Data Errors

    Radiometer America Inc. is recalling ABL90 FLEX analyzers because they may not use the most recent calibration data, potentially leading to biased patient results.

    Product
    ABL90 FLEX analyzer; Model number 393-090. A portable, automated analyzer that measures pH, blood gases, electrolytes, glucose, lactate, bilirubin and oximetry in whole blood.
    Category
    Medical Device
    Distribution
    41 states
  • HighFDA (Food)·F-0969-2015·2015-02-11

    Zilks Roasted Red Pepper Hummus Recalled for Undeclared Peanuts

    Zilks Foods is recalling 4,008 cups of Roasted Red Pepper Hummus due to potential undeclared peanuts in the cumin ingredient.

    Product
    Hummus; All-natural ZILKS ROASTED RED PEPPER HUMMUS GLUTEN FREE & NON-GMO NET WT. 8 OZ
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1055-2015·2015-02-11

    BD 10 mL Syringes Recalled Due to Improperly Seated Stopper

    Becton Dickinson is recalling 564,000 units of 10 mL syringes because the stopper is not properly seated in the syringe.

    Product
    BD 10 mL Syringe BD Luer-Lok Tip with Blunt Plastic Cannula, Not for Skin Injection ; Catalog #303348, BD 10 mL Syringe Luer-Lok Tip with Blunt Fill Needle 18G x 1 1/2 (1.2mm x 40 mm), not for skin injection; Catalog #305064 BD 10 mL Syringe Luer-Lok Tip with BD…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0968-2015·2015-02-11

    Zilks Hummus Recalled for Potential Undeclared Peanuts

    Zilks Foods is recalling 4,768 cups of hummus nationwide due to potential undeclared peanuts in the cumin ingredient.

    Product
    Hummus; All-natural ZILKS FAMOUS ORIGINAL HUMMUS GLUTEN FREE & NON-GMO NET WT. 8 OZ
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1052-2015·2015-02-11

    Zimmer Recalls Persona Tibial Articular Surface Provisional Shims Due to Cleaning Defect

    Zimmer, Inc. is recalling Persona Tibial Articular Surface Provisional Shims because repeated sonic cleaning can break the ball bearing retention feature, potentially leaving parts in the surgical wound.

    Product
    Persona (TASP) Tibial Articular Surface Provisional Shim, all sizes and Lots Catalog Number: 42-5279-002-00 thru 42-5279-009-04. Product Usage: The Persona TASPs are sterilizable instruments Intended for multiple uses. The TASP components are used to aid the surgeon in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1041-2015·2015-02-11

    Roche Cobas b 221 Blood Gas Analyzer Recalled for Measurement Bias

    Roche Diagnostics is recalling 103 Cobas b 221 analyzers because bacterial contamination causes inaccurate glucose and lactate readings.

    Product
    Cobas b 221 (versions 5 and 6) Blood Gas and Electrolytes Analyzer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0974-2015·2015-02-11

    Zilks Hummus with Real Bacon Recalled for Potential Undeclared Peanuts

    Zilks Foods is recalling 3,808 cups of hummus with real bacon due to potential undeclared peanuts in the cumin ingredient.

    Product
    Hummus; All-natural ZILKS HUMMUS with REAL BACON GLUTEN FREE & NON-GMO NET WT. 8 OZ
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1053-2015·2015-02-11

    CareFusion Recalls SmartSite Infusion Sets Due to Disconnection and Leakage

    CareFusion is recalling 7,440 SmartSite Low Sorbing Infusion Sets due to disconnection and leakage issues.

    Product
    SmartSite Low Sorbing Infusion Set, Model No. 10015862 The SmartSite Infusion Sets are used to administer fluid and medications through a needle or catheter inserted into the patient's artery or vein. The set is comprised of components commonly found on intravascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1056-2015·2015-02-11

    Siemens ACUSON SC2000 Ultrasound System Control Panel Bolt Recall

    Siemens is recalling 230 ACUSON SC2000 ultrasound systems because a bolt holding the control panel may fail, preventing the panel from locking into position.

    Product
    ACUSON SC2000 Ultrasound System, Model 10433816, component 10040596 - UILK2. The SC2000 ultrasound imaging system is intended for the following applications: Cardiac, Neo-natal and Fetal Cardiac, Pediatric, Transespohageal, Adult Cephalic, Peripheral Vessel, Abdominal…
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1058-2015·2015-02-11

    Puritan Bennett 980 Ventilator Recalled for Occasional GUI Resets

    Covidien is voluntarily recalling 418 Puritan Bennett 980 ventilators due to occasional graphical user interface resets lasting approximately 30 seconds.

    Product
    Puritan Bennett 980 Ventilator System, Model No. PB980 Ventilator (980xxxxxxxx), The Puritan BennettTM 980 Ventilator System is designed for use on Neonatal (NICU) through Adult patient populations who require respiratory support or mechanical ventilation and weigh a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0383-2015·2015-02-11

    Taro Recalls Children's Loratadine Syrup Due to Blue Plastic Presence

    Taro Pharmaceuticals is recalling 36,684 bottles of Children's Loratadine Syrup because blue plastic was found floating in the liquid.

    Product
    Children's Loratadine Syrup (Loratadine Oral Solution) 5 mg/5 mL, Antihistamine, Grape Flavored Syrup, 24 Hour Non-Drowsy Allergy Relief Sugar Free, 4 FL OZ (120 mL) Bottles, Distributed by: Taro Pharmaceuticals U.S.A., Inc. Hawthorne, NY 10532. NDC: 51672-2092-8.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1048-2015·2015-02-11

    Intuitive Surgical Recalls da Vinci Si Wall Charts for Sterilization Inconsistency

    Intuitive Surgical is recalling 1,034 da Vinci Si Wall Charts because they contained incorrect sterilization dry time information inconsistent with the User Manual.

    Product
    da Vinci Si Surgical System, IS3000; - Wall chart for EndoWrist Stapler 45 System. Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1057-2015·2015-02-11

    Medtronic Recalls KYPHON EXPRESS Osteo Introducer System Due to Labeling Error

    Medtronic is recalling 239 units of the KYPHON EXPRESS Osteo Introducer System because the packaging may contain the wrong instrument tips.

    Product
    KYPHON EXPRESS, Osteo Introducer System, Diamond and Bevel, Size 2, REF T34A, QTY: 1EA, Rx only, STERILE R. For use with spinal fixation devices.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1047-2015·2015-02-11

    Fresenius Crit Line in a Clip Monitor Recalled for Display Misinterpretation

    Fresenius Medical Care is recalling 35 Crit Line in a Clip monitors due to a potential for misinterpretation of the Blood Volume slope graphic display.

    Product
    Fresenius Crit Line in a Clip (CLiC) with SW version 2.51 Model Number: CL10041001. A continuous real-time monitor for non-invasive hematocrit, oxygen saturation and percent change in blood volume calculation during hemodialysis treatment.
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1050-2015·2015-02-11

    Hospira Recalls Plum A+ Infusion Systems with Cracked Pole Clamp Assemblies

    Hospira Inc. is recalling 102 Plum A+ Infusion Systems because cracked pole clamp assemblies prevent the devices from securely attaching to IV poles.

    Product
    Plum A+ Infusion System with Hospira MedNet List 20792-04-25, Pole Clamp Assembly Part Number 820-95443-008. A cassette based multi-function infusion system. Each system includes a pumping module and an assortment of disposable IV sets, optional accessories, and an operator's…
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1043-2015·2015-02-11

    Stryker Recalls Trident PSL Hip Shells Missing Dome Hole Plugs

    Stryker Howmedica Osteonics is recalling seven units of Trident PSL HA Solid Back 50 mm hip shells because the dome hole plugs were missing from the packages.

    Product
    Trident PSL HA Solid Back 50 mm Includes Dome Hole Plug Ref 540-11-50E Intended for cementless application in a total hip arthroplasty procedure. This system is a two piece ( a shell and a liner) design that is assembled during surgery. The shell is press-fit into the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0942-2015·2015-02-11

    Gemini Foods Recalls Dried Bean Curd Due to Dimethyl Yellow Contamination

    Gemini Foods is recalling dried bean curd products because they may be contaminated with dimethyl yellow. The recall covers 3,360 units distributed nationwide.

    Product
    Dried Bean Curd Anka Flavor 24x150g, Item No. 8535
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1033-2015·2015-02-11

    Express Diagnostics Recalls DrugCheck Ketamine Dip Tests for False Positives

    Express Diagnostics is recalling DrugCheck Ketamine Dip Tests because they may produce false positive results, leading to incorrect screening outcomes.

    Product
    DrugCheck Ketamine Dip Test 31317-3P PRO-EU-SWE, 31226-3-CA-GML, 30842 TR, 30108C, 30108C CAN, 30108C EU, and 30108C INT. This assay provides only a preliminary analytical test result.
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-1037-2015·2015-02-11

    FDA Recalls 16cm Minimally Invasive Attachment Due to Incorrect Color Bands

    The Anspach Effort, Inc. is recalling 8 units of the MIA16-G1 Minimally Invasive Attachment because customer complaints indicated the color bands were not correct.

    Product
    16cm Minimally Invasive Attachment. For use with Motor Systems for cutting and shaping bones, including the spine and cranium. Model MIA16-G1
    Category
    Medical Device
    Distribution
    2 states
  • SevereNHTSA·15T004000·2015-02-10

    Tireco Recalls Milestar Tires Due to Sidewall Cracking Risk

    Tireco is recalling specific Milestar tires manufactured in 2014 because they may crack in the lower sidewall, increasing the risk of sudden failure and crashes.

    Product
    TIRES:SIDEWALL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·029-2015·2015-02-10

    Sunrise Poultry Recalls Chicken Products Lacking Import Inspection

    Sunrise Poultry Processors is recalling approximately 2,705 pounds of chicken products that were not inspected at the U.S. point of entry.

    Product
    Canada Firm Recalls Poultry Products Produced Without Benefit of Import Inspection
    Category
    Food
    Distribution
    1 state
  • SevereUSDA FSIS·030-2015·2015-02-10

    Whole Foods Recalls Ready-to-Eat Chili and Burritos for Undeclared Peanut

    Whole Foods Markets is recalling approximately 33,191 pounds of ready-to-eat products, including chilis and burritos, due to misbranding and an undeclared peanut allergen.

    Product
    Whole Foods Markets, Inc. Recalls Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    13 states
  • SevereNHTSA·15V081000·2015-02-10

    Toyota Recalls 2014 FJ Cruiser for Steering Shaft Weld Defect

    Toyota is recalling 2014 FJ Cruisers due to a potential inadequate weld on the intermediate steering shaft, which could lead to loss of steering control.

    Product
    TOYOTA — TOYOTA FJ CRUISER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V082000·2015-02-10

    Mercedes-Benz Recalls 2015 Sprinter 2500 and 3500 for Door Defect

    Mercedes-Benz is recalling 2015 Sprinter 2500 and 3500 vans because an incorrectly installed door component may make doors harder to open after a severe frontal crash.

    Product
    MERCEDES BENZ — MERCEDES BENZ SPRINTER 3500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15076·2015-02-10

    Marin Recalls 2014 MBX 50 and Tiny Trail Children's Bicycles

    Marin Mountain Bikes is recalling 2014 MBX 50 and Tiny Trail children's bicycles because handlebars can loosen or separate, posing a crash and injury risk.

    Product
    2014 Marin MBX 50 and Tiny Trail Bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V080000·2015-02-10

    Forest River Recalls 2014 Rockwood and Flagstaff RVs for Fire Risk

    Forest River is recalling 726 model year 2014 Rockwood and Flagstaff recreational vehicles equipped with the Chill Chaser option due to a fire risk from loose wiring or foam insulation contacting the heating element.

    Product
    FOREST RIVER — FOREST RIVER ROCKWOOD, FLAGSTAFF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V079000·2015-02-09

    Nova Bus Recalls 2009 LFS Transit Buses for Brake Hose Fitting Defect

    Nova Bus is recalling 2009 LFS transit buses because damaged brake hose crimping rings may fail, affecting braking performance and increasing crash risk.

    Product
    NOVA BUS — NOVA BUS NOVA LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V077000·2015-02-09

    Nova Bus Recalls 2007-2009 LFS Transit Buses for Fire Risk

    Nova Bus is recalling 2007-2009 LFS transit buses because a battery cable may short to ground, increasing the risk of a fire.

    Product
    NOVA BUS — NOVA BUS NOVA LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V076000·2015-02-09

    Nova Bus Recalls 2008 LFS Transit Buses for Emergency Exit Defect

    Nova Bus is recalling 2008 LFS transit buses because surrounding material may interfere with opening emergency exit windows, increasing injury risk.

    Product
    NOVA BUS — NOVA BUS NOVA LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V078000·2015-02-09

    Nova Bus Recalls 2009 LFS Transit Buses Due to Wiring Defect

    Nova Bus is recalling 2009 LFS transit buses because an incorrectly wired main power relay circuit may defeat circuit protection, increasing the risk of fire.

    Product
    NOVA BUS — NOVA BUS NOVA LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V072000·2015-02-06

    Nova Bus Recalls 2006 LFS Transit Buses for Brake Air Line Defect

    Nova Bus is recalling 2006 LFS transit buses because incorrectly positioned retaining rings may allow rear brake air lines to detach, increasing crash risk.

    Product
    NOVA BUS — NOVA BUS NOVA LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V071000·2015-02-06

    Nova Bus Recalls 2009-2010 LFS Transit Buses for Axle Shaft Defect

    Nova Bus is recalling 2009-2010 LFS transit buses with ZFAV132 rear axles due to inadequate surface treatment on axle half shafts that may fail and disable the vehicle.

    Product
    NOVA BUS — NOVA BUS NOVA LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V069000·2015-02-06

    Land Rover Recalls 2015 LR4 and Range Rover Sport for Engine Defect

    Land Rover is recalling two 2015 vehicles due to improperly torqued engine bolts that could cause the engine to seize, increasing crash risk.

    Product
    LAND ROVER — LAND ROVER LR4, RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V067000·2015-02-06

    Newmar Recalls 2013-2014 King Aire and Essex Due to Steering Defect

    Newmar is recalling 2013-2014 King Aire and Essex vehicles because steering linkage castlenuts may loosen, potentially causing loss of vehicle control.

    Product
    NEWMAR — NEWMAR ESSEX, KING AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V070000·2015-02-06

    Altec Recalls 2005-2013 Crane Telescopic Jibs Due to Pin Placement Risk

    Altec is recalling 724 crane telescopic jibs from 2005-2013 because the limiting pin may not be inserted correctly, allowing unimpeded movement that could injure operators or nearby individuals.

    Product
    ALTEC — ALTEC CRANE TELESCOPIC JIB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V068000·2015-02-06

    OBS Recalls School Buses with Cracking Wheelchair Lifts

    OBS is recalling certain school buses equipped with Ricon wheelchair lifts where the platform side plate may crack, posing an injury risk to operators.

    Product
    COLLINS — COLLINS, BLUE BIRD, OBS MIDSTAR 20IS, A3FE2803A, CHEVY CG33803, BBCV3011S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15T003000·2015-02-06

    Toyo Open Country M/T Tires Recalled for Tread Separation Risk

    Toyo is recalling specific Open Country M/T tires due to off-center belts that may cause tread separation or loss of inflation pressure, increasing crash risk.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15073·2015-02-05

    Sea Gull Lighting Recalls Chandeliers Due to Falling Hazard

    Sea Gull Lighting is recalling about 8,800 chandeliers in the U.S. and 800 in Canada because the screw collar can break, causing the fixture to fall.

    Product
    Light chandeliers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0865-2015·2015-02-04

    SunBurst Foods Recalls Sausage Dogs for Listeria monocytogenes Contamination

    SunBurst Foods is recalling specific lots of Sausage Dogs due to potential Listeria monocytogenes contamination. Consumers in North Carolina, New Jersey, and South Carolina should not eat these products.

    Product
    Sausage Dog, Net Wt. 4.2 oz., UPC 7-01248-00337-1, MFG Code 1042, Sausage Dog, Net Wt. 4.25 oz., UPC 7-01248-00337-1, MFG Code 1042
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0863-2015·2015-02-04

    SunBurst Foods Recalls Hamburger Due to Listeria monocytogenes Contamination

    SunBurst Foods, Inc. is recalling 3.00 oz. hamburger products in North Carolina, New Jersey, and South Carolina due to potential Listeria monocytogenes contamination.

    Product
    Hamburger, Net Wt. 3.00 oz., UPC 7-01248-00884-0, MFG Code 1591
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0810-2015·2015-02-04

    SunBurst Foods Recalls Country Link Sausage Due to Listeria Risk

    SunBurst Foods is recalling Country Link Sausage (on bun) because it may contain Listeria monocytogenes. The product was distributed in North Carolina, New Jersey, and South Carolina.

    Product
    Country Link Sausage (on bun), Net Wt. 3.50 oz., UPC 7-01248-00120-9, MFG Code 121
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0921-2015·2015-02-04

    SunBurst Foods Recalls Pimento Cheese Due to Listeria Risk

    SunBurst Foods is recalling specific lots of Pimento Cheese on White because they may contain Listeria monocytogenes. The product was distributed in North Carolina, New Jersey, and South Carolina.

    Product
    Pimento Cheese on White, Net Wt. 4.30 oz., UPC 7001248-01099-7, MFG Code 1815
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0811-2015·2015-02-04

    SunBurst Jumbo Breakfast Sausage Ham Egg Cheese Recalled for Listeria

    SunBurst Foods is recalling Jumbo Breakfast sandwiches due to a potential Listeria monocytogenes contamination.

    Product
    Jumbo Breakfast (Sausage, Ham, Egg & Cheese on Bun), Net Wt. 5.25 oz., UPC 7-01248-00507. MFG Code 607
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0833-2015·2015-02-04

    SunBurst Foods Recalls Robust Spaghetti With Meat Sauce Due To Listeria

    SunBurst Foods is recalling Robust Spaghetti w/Meat Sauce because it may contain Listeria monocytogenes. The product was distributed in North Carolina, New Jersey, and South Carolina.

    Product
    Robust Spaghetti w/Meat Sauce, Net Wt. 8.00 oz., UPC 7-01248-00806-2, MFG Code 1560
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0905-2015·2015-02-04

    SunBurst Foods Recalls Cherry Crunch Cake Due to Listeria Risk

    SunBurst Foods is recalling specific lots of Cherry Crunch Cake because of a potential Listeria monocytogenes contamination.

    Product
    Cherry Crunch Cake, Net Wt. 4.50 oz. UPC 7-01248-01038-6, MFG Code 1750
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0854-2015·2015-02-04

    SunBurst Foods Recalls Ham and Turkey Subs Due to Listeria Risk

    SunBurst Foods is recalling specific lots of Ham & Turkey Subs due to a potential Listeria monocytogenes contamination.

    Product
    Two 1/2 Foot Ham & Turkey Sub, Net Wt. 11.30 oz., UPC 7-01248-00939-7, MFG Code 1648
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0837-2015·2015-02-04

    SunBurst Foods Recalls Cheesy Eggs with Link Sausage Due to Listeria Risk

    SunBurst Foods is recalling Cheesy Eggs w/Link Sausage & Dinner Roll because it may contain Listeria monocytogenes. The product was distributed in North Carolina, New Jersey, and South Carolina.

    Product
    Cheesy Eggs w/Link Sausage & Dinner Roll, Net Wt. 7.50 oz., UPC 7-01248-00619-8, MFG Code 1518
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0853-2015·2015-02-04

    SunBurst Foods Recalls Twin Sausage Biscuits Due to Listeria Risk

    SunBurst Foods is recalling Twin Sausage Biscuits because they may be contaminated with Listeria monocytogenes. The product was distributed in North Carolina, New Jersey, and South Carolina.

    Product
    Twin Sausage Biscuits, Net Wt. 3.50 oz., UPC 7-01248-00126-1, MFG Code 127
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0915-2015·2015-02-04

    SunBurst Foods Recalls Pancake with Sausage Due to Listeria Risk

    SunBurst Foods is recalling specific lots of Pancake w/Sausage due to a potential Listeria monocytogenes contamination risk.

    Product
    Pancake w/Sausage, Net Wt. 4.50 oz., UPC 7-01248-00628-1, MFG Code 1528
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0804-2015·2015-02-04

    SunBurst Foods Recalls Combo Sandwiches Due to Listeria Risk

    SunBurst Foods is recalling specific Combo Sandwiches (Ham, Bologna & Cheese) due to a potential Listeria monocytogenes contamination risk.

    Product
    Combo Sandwich (Ham, Bologna & Cheese), Net Wt. 4.00 oz., UPC 7-01248-00532-0, MFG Code 638
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0849-2015·2015-02-04

    SunBurst Foods Recalls Turkey on Wheat Sandwiches Due to Listeria Risk

    SunBurst Foods is recalling specific lots of Turkey on Wheat sandwiches because they may be contaminated with Listeria monocytogenes.

    Product
    Turkey on Wheat, Net Wt. 3.40 oz., UPC 7-01248-00110-1, MFG Code 111
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0836-2015·2015-02-04

    SunBurst Foods Recalls French Toast with Sausage Due to Listeria Risk

    SunBurst Foods is recalling French Toast with Sausage because it may be contaminated with Listeria monocytogenes. The product was distributed in North Carolina, New Jersey, and South Carolina.

    Product
    French Toast w/Sausage, Net Wt. 4.00 oz., UPC 7-01248-00607-5, MFG Code 1506
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0906-2015·2015-02-04

    SunBurst Foods Recalls Peach Cobbler Due to Listeria Risk

    SunBurst Foods is recalling specific lots of Peach Cobbler because of a potential Listeria monocytogenes contamination.

    Product
    Peach Cobbler, Net Wt. 5.10 oz. UPC 7-01248-00848-2, MFG Code 695
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0846-2015·2015-02-04

    SunBurst Foods Recalls Ham & Cheese Croissants Due to Listeria Risk

    SunBurst Foods is recalling specific Ham & Cheese Croissants due to a potential Listeria monocytogenes contamination. Consumers in North Carolina, New Jersey, and South Carolina should check their pantries.

    Product
    Ham & Cheese Croissant, Net Wt. 5.50 oz., UPC 7-01248-01097-3, MFG Code 1813
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0922-2015·2015-02-04

    SunBurst Foods Recalls Single Hot Dog with Chili Due to Listeria Risk

    SunBurst Foods is recalling Single Hot Dog w/Chili products due to a potential Listeria monocytogenes contamination. The recall affects products distributed in North Carolina, New Jersey, and South Carolina.

    Product
    Single Hot Dog w/Chili, Net Wt., 3.10 oz., UPC 7-01248-00800-0, MFG Code 285
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0896-2015·2015-02-04

    SunBurst Foods Recalls Turkey and Provolone Sandwiches Due to Listeria Risk

    SunBurst Foods is recalling specific lots of Turkey and Provolone on Marble Rye sandwiches due to a potential Listeria monocytogenes contamination.

    Product
    Turkey and Provolone on Marble Rye, Net Wt. 4.55 oz., UPC 7-01248-01088-1, MFG Code 1804
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0857-2015·2015-02-04

    SunBurst Foods Recalls Chicken Fillet Sandwiches Due to Listeria Risk

    SunBurst Foods is recalling specific chicken fillet sandwiches due to a potential Listeria monocytogenes contamination.

    Product
    Chicken Fillet w/Swiss Cheese (on bun), Net Wt. 5.50 oz., UPC 7-01248-00150-6, MFG Code 168
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0891-2015·2015-02-04

    SunBurst Foods Recalls Grilled Chicken Pretzel Rolls Due to Listeria Risk

    SunBurst Foods is recalling specific lots of Grilled Chicken Pretzel Rolls because they may be contaminated with Listeria monocytogenes.

    Product
    Grilled Chicken Pretzel Roll, Net Wt. 7.00 oz., UPC 7-01248-01082-9, MFG Code 1798
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0917-2015·2015-02-04

    SunBurst Foods Recalls Chicken Tenders Due to Listeria Risk

    SunBurst Foods is recalling specific lots of Chicken Tenders due to a potential Listeria monocytogenes contamination.

    Product
    Chicken Tenders, Net Wt. 8.00 oz., UPC 7-01248-00942-7, MFG Code 1651
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0935-2015·2015-02-04

    Fisher Chopped Walnuts Recalled Due to Possible Salmonella Contamination

    John B. Sanfilippo & Son Inc. is recalling Fisher brand chopped walnuts due to possible Salmonella contamination. The product was distributed in five US states.

    Product
    Chopped walnuts packaged in 8 oz. (226 g) plastic bags under the Fisher brand.
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-0851-2015·2015-02-04

    SunBurst Foods Recalls Sausage and Egg Sandwiches Due to Listeria

    SunBurst Foods is recalling Sausage & Egg sandwiches because they may contain Listeria monocytogenes. The product was distributed in North Carolina, New Jersey, and South Carolina.

    Product
    Sausage & Egg (on bun), Net Wt. 3.75 oz., UPC 7-01248-00130-8, MFG Code 131
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0806-2015·2015-02-04

    SunBurst Foods Recalls Ham and Cheese Sandwiches for Listeria Risk

    SunBurst Foods is recalling specific lots of Ham & Cheese on Wheat sandwiches due to a potential Listeria monocytogenes contamination.

    Product
    Ham & Cheese on Wheat, Net Wt. 3.00 oz., UPC 7-01248-00827-7, MFG Code 1035; Ham & Cheese on Wheat, Net Wt. 3.80 oz., UPC 7-01248-01095-9, MFG Code 1811
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0938-2015·2015-02-04

    Farm Country Cheese House Recalls Raw Milk Cheddar Cheese for Listeria Risk

    Farm Country Cheese House, Inc. is recalling raw milk cheddar cheese due to potential Listeria monocytogenes contamination. The product was distributed in Michigan.

    Product
    Raw Milk Cheddar Cheese, packaged in 8-oz. blocks and 5-lb. loafs.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-0908-2015·2015-02-04

    SunBurst Foods Recalls Carrots with Buttermilk Ranch Dressing Due to Listeria

    SunBurst Foods is recalling Carrots with Buttermilk Ranch Dressing due to a potential Listeria monocytogenes contamination. The product was distributed in North Carolina, New Jersey, and South Carolina.

    Product
    Carrots with Buttermilk Ranch Dressing, Net Wt. 2.50 oz. UPC 7-01248-01070-6, MFG Code 1785
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0884-2015·2015-02-04

    SunBurst Foods Recalls Turkey and Cheese Sandwiches Due to Listeria Risk

    SunBurst Foods is recalling specific lots of Turkey and Cheese on White sandwiches due to a potential Listeria monocytogenes contamination.

    Product
    Turkey and Cheese on White, Net. Wt. 3.80 oz., UPC 7-01248-01090-4, MFG Code 1806
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0889-2015·2015-02-04

    SunBurst Deli Ham and Cheese on Marble Rye Recalled for Listeria

    SunBurst Foods is recalling Deli Ham and Cheese on Marble Rye due to a Listeria monocytogenes hazard. The product was distributed in North Carolina, New Jersey, and South Carolina.

    Product
    Deli Ham and Cheese on Marble Rye, Net Wt. 5.55 oz., UPC 7-01248-01094-2, MFG Code 1810
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0820-2015·2015-02-04

    SunBurst Grilled Cheese Recalled for Listeria monocytogenes Contamination

    SunBurst Foods is recalling Grilled Cheese products due to Listeria monocytogenes contamination. The products were distributed in North Carolina, New Jersey, and South Carolina.

    Product
    Grilled Cheese, Net. Wt. 1.65 oz., UPC 7-01248-00883-3, MFG Code 1593
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0919-2015·2015-02-04

    SunBurst Foods Recalls Western Omelet Due to Listeria Risk

    SunBurst Foods is recalling specific lots of Western Omelet because they may be contaminated with Listeria monocytogenes.

    Product
    Western Omelet, Net WT. 8.25 oz., UPC 7-01248-00650-1, MFG Code 1551
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0868-2015·2015-02-04

    SunBurst Foods Recalls Smoking Joe Smoked Sausage on Bread for Listeria

    SunBurst Foods is recalling Smoking Joe Smoked Sausage on Bread due to a potential Listeria monocytogenes contamination.

    Product
    Smoking Joe (Smoked Sausage on Bread), Net Wt. 5.25 oz., UPC 7-01248-00122-3, MFG Code 123
    Category
    Food
    Distribution
    3 states

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