The Recall Desk

Archive

March 2014 recalls

554 recalls were announced in March 2014.

What the numbers show

Critical
40
Severe
195
High
194
Moderate
113
Low
12

Of the 554 recalls this month scored against our rubric, 7% are Critical, 35% are Severe.

Which agencies issued them

501–554 of 554

  • HighFDA (Devices)·Z-1097-2014·2014-03-05

    Ossur Recalls Symbionic Leg Due to Battery Warning Failure

    Ossur is recalling 144 Symbionic Leg prosthetics because they fail to display a low battery warning before powering down.

    Product
    The SYMBIONIC LEG is an integrated prosthetic leg for transfemoral and knee disarticulation amputees. Product Usage: SYMBIONIC LEG is intended for continuous use by amputees of low to moderate impact levels that weigh less than 125 kg for foot categories 25 30 and less…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1553-2014·2014-03-05

    Popcorn Factory Recalls Heart-Shaped Popcorn Balls Due to Missing Allergen Labels

    The Popcorn Factory is recalling heart-shaped popcorn balls because the Nutrition Facts and allergen labels were not applied to the individual pieces. The product contains milk and soy allergens.

    Product
    Candy coated popcorn shaped into a heart weighing 1.5 ounces per piece and individually wrapped in clear plastic packaging. There are 24 popcorn balls per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1066-2014·2014-03-05

    Smith & Nephew Recalls Reflection Interfit Shell Due to Undersized Radius

    Smith & Nephew is recalling 10 units of Reflection Interfit Shells because the inner spherical radius is undersized. The affected devices were distributed in the US and internationally.

    Product
    Reflection Interfit Shell, 52 MM OD, 3 HOLE, REF 71336052, QTY 1, STERILE R, Smith & Nephew, Inc. Indications for use include cemented or uncemented total hip arthroplasty for rheumatoid arthritis; osteoarthritis; post traumatic arthritis, avascular necrosis; femoral and neck…
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-1099-2014·2014-03-05

    Fresenius Optiflux F160NR Dialyzers Recalled for Dialysate Port Leak

    Fresenius Medical Care is recalling Optiflux F160NR dialyzers because the dialysate port may leak during priming. The recall covers 6,720 units distributed in the US and Mexico.

    Product
    Optiflux F160NR High Flux Dialyzers; Product Number: 0500316N. Single Use acute or chronic hemanalysis treatment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1075-2014·2014-03-05

    Radiometer D788 pCO2 Membranes Recalled for Biased Measurement Results

    Radiometer America is recalling D788 pCO2 membranes because they may cause biased measurement results for patients and quality control.

    Product
    pCO2 D788 Membranes. Distributed by Radiometer America, Inc., Westlake, OH. An automatic or semi-automatic instrument used to identify and quantify two or more gases, and sometimes electrolytes, in whole blood using multiple special electrodes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1585-2014·2014-03-05

    E. Franco & Co. Recalls Brazo Gitano Cakes for Undeclared Wheat

    E. Franco & Co. Inc is recalling Brazo Gitano rolled cakes with chocolate filling due to undeclared wheat. The product was distributed in Puerto Rico.

    Product
    "***Brazo gitano (rolled cake)***chocolate filling***"
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1108-2014·2014-03-05

    Philips HeartStart MRx Defibrillators Recalled for Wireless Data Transmission Defect

    Philips is recalling 220 HeartStart MRx defibrillators because the Wireless Link upgrade may fail to transmit data in specific configurations.

    Product
    M3536A HeartStart MRx with Wireless Link Upgrade (861289) The HeartStart MRx is for use for the termination of ventricular tachycardia and ventricular fibrillation. The device is for use by qualified medical personnel trained in the operation of the device and qualified by…
    Category
    Medical Device
    Distribution
    21 states
  • HighFDA (Devices)·Z-1106-2014·2014-03-05

    Fresenius Recalls Optiflux F18Nre Dialyzers Due to Port Leak Risk

    Fresenius Medical Care is recalling 34,752 Optiflux F18Nre Flux Dialyzers because the dialysate port may leak during priming.

    Product
    Optiflux F18Nre Flux Dialyzers; Product Number: 0500308E. Single Use acute or chronic hemanalysis treatment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1579-2014·2014-03-05

    E. Franco & Co. Recalls Brazo Gitano Rolls for Undeclared Wheat

    E. Franco & Co. Inc is recalling approximately 2,300 14-ounce rolls of Brazo Gitano with chocolate cake filling distributed in Puerto Rico due to undeclared wheat.

    Product
    "***Brazo gitano (rolled cake)***chocolate cake filling***"
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1080-2014·2014-03-05

    Siemens Artis zee Ceiling Systems Recalled for Cable Damage Risk

    Siemens Medical Solutions USA is recalling 284 Artis zee Ceiling Systems due to potential cable damage from sub-optimal guidance.

    Product
    Siemens Artis zee Ceiling Systems. Angiographic x-ray system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1103-2014·2014-03-05

    Fresenius Optiflux F200NR Dialyzers Recalled for Dialysate Port Leak

    Fresenius Medical Care is recalling 19,596 Optiflux F200NR dialyzers due to a dialysate port leak during priming. The units were distributed in the US and Mexico.

    Product
    Optiflux F200NR High Flux Dialyzers; Product Number: 0500320N. Single Use acute or chronic hemanalysis treatment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1567-2014·2014-03-05

    Mars Recalls Uncle Ben's Saffron Rice Due to Mild Flushing Reports

    Mars Food US is recalling Uncle Ben's Infused Rice Saffron Flavor after reports of mild flushing reactions that resolved within two hours.

    Product
    Uncle Ben's (R), Infused(R) Rice Saffron Flavor, net weight 5 LB (2.27kg), Distributed by MARS foodservices US, P.O. Box 11547, Carson, CA 90749-11547
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1088-2014·2014-03-05

    Actavis Recalls Subpotent Gelnique Oxybutynin Chloride Gel Samples

    Actavis is recalling Gelnique (oxybutynin chloride) Gel 10% physician samples because drug potency was compromised during shipment.

    Product
    Gelnique (oxybutynin chloride) Gel 10%, 100 mg in 1 g sachet, for topical use only. Physician sample in clamshell container with seven heat-sealed sachets. Rx Only. Watson Pharmaceuticals Inc, Corona, CA, 92890. NDC: 52544-084-77.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1564-2014·2014-03-05

    Mars Recalls Uncle Ben's Rice Due to Mild Flushing Reports

    Mars Food US is recalling Uncle Ben's Infused Rice Roasted Chicken Flavor after reports of mild flushing reactions that resolved within two hours.

    Product
    Uncle Ben's (R), Infused(R) Rice Roasted Chicken Flavor, net weight 5 LB (2.27 kg) and 25 LB (11.34 kg), Distributed by MARS foodservices US, P.O. Box 5059, Rancho Dominguez, CA 90224-5059
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1563-2014·2014-03-05

    Mars Recalls Uncle Ben's Infused Rice Mexican Flavor Due to Flushing Reports

    Mars Food US is recalling Uncle Ben's Infused Rice Mexican Flavor after reports of mild flushing reactions that resolved within two hours.

    Product
    Uncle Ben's (R), Infused(R) Rice Mexican Flavor, net weight 5 LB (2.27 kg) and 25 LB (11.34 kg), Distributed by MARS foodservices US, P.O. Box 5059, Rancho Dominguez, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1590-2014·2014-03-05

    Mars Recalls Uncle Ben's Infused Rice Cheese Flavor Due to Flushing Reports

    Mars Food US is recalling Uncle Ben's Infused Rice Cheese Flavor nationwide after reports of mild flushing reactions that resolved within two hours.

    Product
    Uncle Ben's (R), Infused(R) Rice Cheese Flavor, net weight 5 LB (2.27 kg), Distributed by MARS foodservices US, P.O. Box 11547, Carson, CA 90749-1547
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1592-2014·2014-03-05

    Newman's Own Coffee K-Cups Recalled for Decaffeinated Labeling Errors

    Green Mountain Coffee Roasters is recalling 8,928 boxes of Newman's Own Organic Coffee K-Cups because some caffeinated packs were incorrectly labeled as decaffeinated.

    Product
    Newmans Own¿ Organics Newmans Special Blend 80 Count K-Cup¿ Packs; UPC 09955515593; Product Code: 15593 281792
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1087-2014·2014-03-05

    Ortho VITROS Sodium Slides Recalled for False Positive Results

    Ortho Clinical Diagnostics is recalling VITROS Na+ Slides and Calibrator Kit 2 because they may produce false positive sodium results in serum and plasma samples.

    Product
    VITROS Chemistry Products Na+ Slides, manufactured by Ortho Clinical Diagnostics 513 Technology Blvd Rochester, NY 14652 VITROS Na+ Slides quantitatively measure sodium (Na+) concentration in serum, plasma, and urine using VITROS 250/350/950/5,1 FS and 4600 Chemistry Systems…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1087-2014·2014-03-05

    Actavis Recalls Clonazepam Tablets Due to Subpotent Tablet Weight

    Actavis Elizabeth LLC is recalling 13,608 bottles of Clonazepam 2 mg tablets because routine testing found one tablet with weight below specification.

    Product
    Clonazepam Tablets, USP 2 mg 100 tablets Manufactured by: Actavis Elizabeth LLC 200 Elmora Avenue, Elizabeth, NJ 0737 USA NDC 0228-3005-11 packaged in White/Round HDPE 75 CC with white/round plastic 33 mm CRC closure shipped in corrugated 75 cc carton (24 bottles/carton)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1094-2014·2014-03-05

    Hologic Recalls NovaSure Radiofrequency Controllers for Electrical Standard Non-Compliance

    Hologic is recalling 93 NovaSure Radiofrequency Controllers because they may not meet the IEC 60601-1 electrical safety standard.

    Product
    NovaSure Impedance Controlled Endometrial Ablation System Radiofrequency Controller, Model Number: 71978-001 Catalog Number: RFC2009 Product Usage: The NovaSure Impedance Controlled Endometrial Ablation System is intended to ablate the endometrial lining of the uterus in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1076-2014·2014-03-05

    Siemens Dimension Vista Enzyme 1 Calibrator Recalled for QC Shifts

    Siemens Healthcare Diagnostics is recalling specific lots of Dimension Vista Enzyme 1 Calibrator due to quality control shifts and imprecision during Pseudocholinesterase calibration.

    Product
    Dimension Vista Enzyme 1 Calibrator (ENZ 1 CAL) lots 3FD034 and 3HD012. An in vitro diagnostic multi-analyte calibrator for the calibration of Amylase (AMY), Gamma-Glutamyl Transferase (GGT), Lactate Dehydrogenase (LDH), Lipase (LIPL), and Pseudocholinesterase (PCHE) methods…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1088-2014·2014-03-05

    Ortho VITROS Chemistry Calibrator Kit 2 Recalled for False Positive Results

    Ortho Clinical Diagnostics is recalling VITROS Chemistry Products Calibrator Kit 2 because it may produce false positive serum and plasma sample results.

    Product
    VITROS Chemistry Products Calibrator Kit 2, manufactured by Ortho Clinical Diagnostics 1000 Lee Road Rochester, NY 14606 VITROS Chemistry Products Calibrator Kit 2 is used to calibrate VITROS 250/350/950/5,1 FS and 4600 Chemistry Systems and the VITROS 5600 Integrated System…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1068-2014·2014-03-05

    Smith & Nephew Recalls Renasys EZ PLUS Canisters for Labeling Changes

    Smith & Nephew is recalling Renasys EZ PLUS canisters to modify the bacterial overflow guard and update product labeling.

    Product
    Renasys EZ PLUS, a Canister Component of of Renasys EZ Negative Pressure Wound Therapy System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1067-2014·2014-03-05

    Smith & Nephew Recalls Renasys EZ Canisters for Labeling and Filter Changes

    Smith & Nephew is recalling Renasys EZ canisters to modify the bacterial overflow guard and update product labeling.

    Product
    Renasys EZ, a Canister Component of of Renasys EZ Negative Pressure Wound Therapy System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1565-2014·2014-03-05

    Mars Recalls Uncle Ben's Garlic & Butter Rice Due to Flushing Reports

    Mars Food US is recalling Uncle Ben's Infused Rice Garlic & Butter Flavor after reports of mild flushing reactions that resolved within two hours.

    Product
    Uncle Ben's (R), Infused(R) Rice Garlic & Butter Flavor, net weight 5 LB (2.27kg), Distributed by MARS foodservices US, P.O. Box 5059, Rancho Dominguez, CA 90224-5059
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1566-2014·2014-03-05

    Mars Recalls Uncle Ben's Rice Pilaf Due to Mild Flushing Reports

    Mars Food US is recalling Uncle Ben's Infused Rice Pilaf after reports of mild flushing reactions that resolved within two hours.

    Product
    Uncle Ben's (R), Infused(R) Rice Pilaf, net weight 5 LB (2.27kg), Distributed by MARS foodservices US, P.O. Box 11547, Carson, CA 90749-11547
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1095-2014·2014-03-05

    Cardiovascular Systems Recalls Diamondback 360 Coronary Orbital Atherectomy Devices

    Cardiovascular Systems, Inc. is recalling 318 Diamondback 360 Coronary Orbital Atherectomy Devices because they mistakenly contain a saline line not approved for coronary use.

    Product
    CSI, Diamondback 360 Coronary Orbital Atherectomy System, Part Number 70058-02, Model Number DBEC-125 Product Usage: The system is indicated to facilitate stent delivery in patients with coronary artery disease (CAD) who are acceptable candidates for PTCA or stenting due to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1107-2014·2014-03-05

    Philips HeartStart XL+ Defibrillator Recalled for Battery Charge Time Labeling Error

    Philips is recalling 7,157 HeartStart XL+ Defibrillators because the battery charge time at high temperatures is slightly longer than the 3 hours stated in the labeling.

    Product
    Philips HeartStart XL+ Defibrillator/Monitor Model: 861290 The HeartStart XL+ is intended for use in a hospital setting by qualified medical personnel trained in the operation of the device and qualified by training in basic life support, advanced life support or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1096-2014·2014-03-05

    Invivo Expression IP5 Information Portal Recalled for Audio Loss

    Invivo Corporation is recalling 271 Expression IP5 Information Portal devices because three units lost audio during use.

    Product
    Invivo Corporation Expression IP5 Information Portal Product Usage: The Expression Information Portal (Model IP5) a display and device controller for Philips MRI patient monitoring systems, is intended for use by trained health care professional to remotely monitor the…
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Food)·F-1568-2014·2014-03-05

    Mars Recalls Uncle Ben's Spanish Flavor Rice Due to Flushing Reports

    Mars Food US is recalling Uncle Ben's Spanish Flavor Rice after reports of mild flushing reactions that resolved within two hours.

    Product
    Uncle Ben's (R), Infused(R) Rice Spanish Flavor, net weight 25 LB (11.34 kg), Distributed by MARS foodservices US, P.O. Box 5059, Rancho Dominguez, CA 90224-5059
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1073-2014·2014-03-05

    NxStage PureFlow-B Solution Recalled for Mislabeled Product

    NxStage Medical is recalling 969 cases of PureFlow-B Solution due to mislabeling. The product is used in hemodialysis systems.

    Product
    NxStage PureFlow-B Solution; Model/Catalog Number: RFP-401. Product is packaged in a case containing two individual 5L bags. The NxStage PureFlow-B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during…
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Drugs)·D-1086-2014·2014-03-05

    Ranbaxy Recalls Atorvastatin Calcium Tablets Due to Foreign Tablet Presence

    Ranbaxy Inc. is recalling 64,626 bottles of Atorvastatin Calcium 10 mg tablets because a 20 mg tablet was found inside a sealed 10 mg bottle.

    Product
    ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1558-2014·2014-03-05

    RCI Produce Recalls Cactus Pads Due to Pesticide Residues

    RCI Produce is recalling MexpoGroup brand cactus pads found to contain pesticides with no US tolerance.

    Product
    Cactus Leaves/Pads (Nopales) MexpoGroup Brand MexpoGroup Fresh Produce Colonia Buenos Aires Norte, Tijuana, Baja California, Mexico.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1111-2014·2014-03-05

    Roche Recalls Leaking cobas PCR Urine and Swab Test Kits

    Roche Molecular Systems is recalling 84 batches of cobas PCR Urine, Female Swab, and media kits due to reports of leaking media.

    Product
    cobas¿ PCR Urine Kit 100 PKT IVD cobas¿ PCR Female Swab Kit 100 PKT IVD cobas¿ PCR media 100T IVD cobas¿ PCR Female Swab Kit 100 PKT JPN-IVD Roche Molecular Systems, Inc. Branchburg, NJ 08876 USA Roche Diagnostics 9115 Hague Road Indianapolis, IN 46250-0457 The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1093-2014·2014-03-05

    Dako HER2 CISH pharmDx Kit Recalled Due to Weak Red Signals

    Dako North America Inc. is recalling 49 units of the HER2 CISH pharmDx Kit because weak red signals have been observed.

    Product
    Product Name: HER2 CISH pharmDx Kit Catalog/Model number: SK109, lot 20000910 Product Usage: For in vitro diagnostic use. HER2 CISH pharmDx Kit is intended for dual-color chromogenic visualization of signals achieved with directly labeled in situ hybridization probes…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1591-2014·2014-03-05

    Novartis Recalls Benefiber Fiber Supplement Stick Packs Due to Consumer Complaints

    Novartis Consumer Health is recalling specific lots of Benefiber fiber supplement stick packs nationwide due to a high number of consumer complaints.

    Product
    Benefiber fiber supplement stick packs, sugar free and taste free, packaged in the following configurations: (1) Benefiber Fiber Supplement, On-The-Go Stick Packs, Sugar Free, Clear & Taste-Free, packaged in 8.16-oz. boxes containing 68/0.12-oz. stick packs, UPC 300670176686.…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1569-2014·2014-03-05

    True Botanica Enzymes Plus Recalled for Chloramphenicol Contamination

    Nature's Value Inc. is recalling True Botanica Enzymes Plus capsules found to contain Chloramphenicol at 9.7 ppb.

    Product
    True Botanica brand Enzymes Plus, 45 CAPSULES, Product No. TB043-45, a Dietary Supplement --- Manufactured for True Botanica LLC, 1005 Richards Rd, Suite D, Hartland, WI 53029
    Category
    Food
    Distribution
    1 state
  • LowFDA (Devices)·Z-1121-2014·2014-03-05

    Medtronic Everest 20cc Inflation Device Recalled for Incorrect Master Label

    Medtronic Vascular is recalling 191 Everest 20cc Inflation Devices due to an incorrect master label. The devices are sterile, single-use tools used to inflate balloon catheters.

    Product
    Medtronic Everest 20cc Inflation Device; Model Number and Catalog Number: AC2205P The Everest 20cc Inflation device is designed to be used to inflate / deflate balloon catheters as well as to monitor pressure within the balloon. The Everest 20atm Device is outfitted with a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1090-2014·2014-03-05

    Gilead Recalls Atripla Tablets Due to Foreign Silicone Particulates

    Gilead Sciences is recalling specific lots of Atripla tablets because they contain red silicone rubber particulates. The recall covers 39,223 bottles distributed nationwide.

    Product
    Atripla (efavirenz 600 mg/ emtricitabine 200 mg/ tenofovir disoproxil fumarate 300 mg) Tablets, 30 Tablet Bottles, Rx only. Manufactured for: Bristol-Myers Squibb & Gilead Sciences, LLC, Foster City, CA 94404. Made in Ireland. NDC 15584-0101-1. Manufactured for…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V087000·2014-03-04

    New Flyer Transit Buses Recalled for Potential Exhaust Fire Risk

    New Flyer is recalling certain transit buses because condensation in the intake manifold may freeze, causing sensor issues that could lead to exhaust flames or vehicle fires.

    Product
    NEW FLYER — NEW FLYER C40LF, C40LFR, C35LF, C35LFR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V095000·2014-03-04

    Prevost Recalls 2013-2014 Coaches Due to Battery Cable Insulation Defect

    Prevost is recalling 59 model year 2013-2014 coaches because defective battery cable insulation may cause the engine to shut down, increasing crash risk.

    Product
    PREVOST — PREVOST H3-45 VIP, H3-45, H3-41
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V097000·2014-03-04

    Ford E-Series CNG Conversion Recall for Rear Cylinder Bracket Failure

    Landi Renzo USA is recalling 2011-2014 Ford E-150, E-250, and E-350 vans modified for CNG because rear cylinder brackets may fail, risking a gas leak and fire.

    Product
    FORD — FORD E-250, E-150, E-350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V103000·2014-03-04

    Fiat 500L Recall: Transmission Shifter May Fail to Shift Gears

    Chrysler is recalling 2014 Fiat 500L vehicles because the transmission shifter may not respond to driver input, potentially causing unintended vehicle movement.

    Product
    FIAT — FIAT 500L
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V098000·2014-03-04

    Newmar Recalls 2013-2014 RVs Due to Microwave Fire Risk

    Newmar is recalling 599 recreational vehicles from 2013-2014 because the built-in microwave may start on its own, posing a fire hazard if contents are inside.

    Product
    NEWMAR — NEWMAR DUTCH STAR, MOUNTAIN AIRE, VENTANA, VENTANA LE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V091000·2014-03-04

    Volvo Bus 9700 Recall: Sliding Seat Locking Defect

    Volvo is recalling 2009-2014 9700 coaches with wheelchair lifts because sliding seats may not latch correctly, increasing injury risk in a crash.

    Product
    VOLVO BUS — VOLVO BUS 9700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V096000·2014-03-04

    Prevost Recalls 2011-2012 Coaches Due to Fire Suppression Tank Issue

    Prevost is recalling 2011-2012 X3 and XLII coaches because the fire suppression tank may discharge prematurely, leaving the system unavailable during a fire.

    Product
    PREVOST — PREVOST X3, XLII
    Category
    Vehicle
    Distribution
    Distributed nationwide

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