The Recall Desk

Archive

February 2013 recalls

297 recalls were announced in February 2013.

What the numbers show

Critical
10
Severe
53
High
170
Moderate
44
Low
20

Of the 297 recalls this month scored against our rubric, 3% are Critical, 18% are Severe.

Which agencies issued them

201–297 of 297

  • ModerateFDA (Food)·F-0980-2013·2013-02-13

    MET-Rx Extreme Thermo Rage Watermelon Supplement Recalled for Spoilage

    NBTY Inc. is recalling MET-Rx Extreme Thermo Rage Watermelon dietary supplements because Acetobacter lovaniensis was detected in a sample. This is a commercial spoilage issue.

    Product
    MET-Rx EXTREME THERMO RAGE WATERMELON DIETARY SUPPLEMENT, 8 FL. OZ. (240 mL) , Product Number 50390 (Bulk number 50389), UPC 7 86560 50389 1, Label Revision 00B --- Manufactured in the USA by MET-RX Nutrition, Inc. Boca Raton, FL 33487
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0744-2013·2013-02-13

    Carestream Recalls Dental Film Due to Missing Label Symbols

    Carestream Health is recalling specific lots of Kodak Insight Dental Film because the clear carton labels are missing required symbols and manufacturer information.

    Product
    KODAK INSIGHT DENTAL FILM in SureSoft Packets, Size 2 Single Packet Film, Model Number IP21S, REF/Catalog Number 8118226 --- COMMON/USUAL NAME: Dental Intraoral Radiographic Film -- 20 cartons of 80 packets. Product Usage: Dental intraoral radiography
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0981-2013·2013-02-13

    NBTY Recalls Pure Protein Grape Flavored Protein Shots

    NBTY Inc. is recalling Pure Protein Grape Flavored Protein Shots due to the detection of Lactobacillus plantarum and Lactobacillus brevis, which indicates commercial spoilage.

    Product
    PURE PROTEIN PROTEIN SHOT 25g PROTEIN, GRAPE Flavor PROTEIN DRINK 2.9 fl. oz. (86 mL), Product Number 50451, Bulk Number 36753 (Vial), UPC 7 49826 50451 3 (Vial), and Product Number 50452, Bulk Number 36753 (Carton of 6), UPC 7 49826 50452 0 (Carton). --- Carefully Manufactured
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-156-2013·2013-02-13

    Bayer Recalls Leukine Sargramostim Vials Due to Impurities

    Bayer HealthCare Pharmaceuticals is recalling Leukine sargramostim vials because a confirmed out-of-specification result for impurities was found in one lot.

    Product
    Leukine sargramostim 5 x 500 mcg/mL vial, liquid injection, Sterile Rx only, Mfd by: Bayer HealthCare Pharmaceuticals, LLC Seattle, WA 98101 U.S. Lic. No. 1791 NDC 58468-0181-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-144-2013·2013-02-13

    Stat Rx USA Recalls Methocarbamol Tablets Due to Incorrect Expiration Date

    Stat Rx USA is recalling 3 bottles of Methocarbamol 750 mg tablets distributed in Pennsylvania because they were labeled with an incorrect expiration date.

    Product
    Methocarbamol 750 mg Tablets, 90-count bottle, Mfg by: West-Ward Pharm. Corp., Eatontown, NJ 07724, Packaged and Distributed by: Stat Rx USA, NDC 42549-521-90.
    Category
    Drug
    Distribution
    1 state
  • LowFDA (Drugs)·D-152-2013·2013-02-13

    Sandoz Recalls Syeda Oral Contraceptives for Incorrect Tablet Imprinting

    Sandoz is recalling Syeda oral contraceptives because some tablets have the wrong ID imprint. Consumers should stop using the affected lot and contact a healthcare provider.

    Product
    Syeda (drospirenone and ethinyl estradiol), 3 mg/0.03 mg, 3 x 28 tablet blistercards, combination oral contraceptive tablet, Manufactured by Laboratorios Leon Farma S.A., Spain for Sandoz Inc., Princeton, NJ
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-146-2013·2013-02-13

    Ascend Recalls EstroGel Pump Defect

    Ascend Therapeutics is recalling 4,835 bottles of EstroGel (estradiol gel) 0.06% because the pump head may detach from the canister.

    Product
    EstroGel (estradiol gel) 0.06%, contained in 50-gr metered pumps, 1.25g/pump depression, for use as physician starter samples; product is labeled in part ***Manufactured for ASCEND Therapeutics Herndon, VA 20170 by DPT Laboratories San Antonio TX 78215***
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0970-2013·2013-02-13

    Siya Pan Gilori Recalled for High Levels of Red Dye and Metals

    Miami Growers Inc. is recalling Siya Pan Gilori because it contains high levels of Red dye 45170-Rhodamine B-Basic Violet 10 and silver leaves and other metals.

    Product
    Siya Pan Gilori Net Wt. 180g. Distributed by: Miami Growers Inc. 80 Broadway Jersey City, NJ 07306 T 201-985-9322, 201-369-1500 Visit us: www.miamigrowersinc.com UPC 0893056003800
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0792-2013·2013-02-13

    Diagnostic Hybrids RhMK Culture Media Recalled for Fungal Contamination

    Diagnostic Hybrids is recalling RhMK culture media due to fungal contamination. The affected products are used to cultivate viruses from patient specimens.

    Product
    Diagnostic Hybrids, Inc., RhMK, Model #:49-0600, 49-0600A, 49-0102A, and 49-T075A. Culture media, used in the cultivation and amplification of viruses, such as respiratory viruses, enteroviruses, measles, and poliovirus from patient specimens.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-151-2013·2013-02-13

    Estee Lauder DayWear Moisturizer Recalled for Potential Sunscreen Instability

    Estee Lauder is recalling DayWear Sheer Tint Release moisturizer because the sunscreen ingredient may be unstable, potentially reducing its effectiveness.

    Product
    ESTEE LAUDER DayWear Sheer Tint Release, Advanced Multi-Protection Anti-Oxidant Moisturizer Broad Spectrum SPF15, All Skin types, 1.7 FL. OZ. LIQ/50 ml (tube inside a unit carton) with UPC No. 2713179904, Code WKEM-01, and 1.5 mL foil sample packets, ESTEE LAUDER, DIST., NEW YO
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·13C001000·2013-02-12

    Recaro Recalls ProSport Child Seats Due to Head Movement Risk

    Recaro is recalling ProSport model 385 child seats because excessive head movement can occur when installed with LATCH anchors only, increasing injury risk.

    Product
    CHILD SEAT:TETHER: CONNECTOR/CLIP recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·13724·2013-02-12

    Bohning Recalls Middleton Siege Crossbows Due to Unexpected Firing Hazard

    Bohning is recalling Middleton Siege Crossbows because they can fire unexpectedly or have limbs that crack. Consumers should stop using them and contact Bohning for a refund.

    Product
    Middleton Siege Crossbows
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V046000·2013-02-11

    Spartan Recalls Aerial Vehicles Due to Inclinometer Signal Failure

    Spartan is recalling 2005-2011 RMP 100 and 2008-2010 MMP 100 aerial vehicles because a faulty inclinometer may allow the platform to tilt dangerously, risking injury or property damage.

    Product
    SPARTAN — SPARTAN RMP 100, MMP 100
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V042000·2013-02-08

    Fontaine Modified Navistar Trucks Recalled for Steering Assembly Defect

    Fontaine Modification is recalling 811 modified Navistar trucks because steering clips may come loose, potentially making the vehicle difficult to steer and increasing crash risk.

    Product
    FONTAINE — FONTAINE INT'L 7400 W/DUAL STEERIN, INT'L 4300 W/DUAL STEERIN, INT'L 4400 W/DUAL STEERIN, INT'L 7500 W/DUAL STEERIN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13E007000·2013-02-08

    Fulmer Motorcycle Helmets Recalled for Safety Standard Non-Compliance

    Fulmer is recalling specific motorcycle helmet models that fail to meet federal safety standards for impact and retention. Owners should contact the manufacturer for a replacement or reimbursement.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V045000·2013-02-07

    BMW Recalls 2007-2010 X5 Vehicles Due to Brake Vacuum Pump Leak

    BMW is recalling 2007-2010 X5 SAVs with 8-cylinder engines because a brake vacuum pump leak may cause loss of power assist braking, increasing stopping distance.

    Product
    BMW — BMW X5 SAV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V039000·2013-02-07

    Prevost Recalls Coaches Due to Throttle Control Software Defect

    Prevost is recalling specific model year 2008-2013 coaches equipped with Volvo engines because a software defect may cause the throttle to remain fixed at 1700 rpm, increasing crash risk.

    Product
    PREVOST — PREVOST XLII-45 ENTERTAINER, H3-45, X3-45, H3-41
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·13117·2013-02-07

    BlueStar Residential Gas Wall Ovens Recalled for Fire Hazard

    Prizer Painter Stove Works is recalling about 940 BlueStar gas wall ovens due to a fire hazard caused by improper installation or damaged gas connectors.

    Product
    BlueStar™ residential gas wall ovens
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·13723·2013-02-07

    BRP Recalls Ski-Doo Snowmobiles Due to Fuel Leak Fire Hazard

    Bombardier Recreational Products is recalling about 10,200 Ski-Doo snowmobiles because a fuel pump fitting can break, causing a fuel leak and fire hazard.

    Product
    Ski-Doo® snowmobiles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·13118·2013-02-07

    Mutsy USA Recalls EVO Strollers Due to Strangulation Hazard

    Mutsy USA is recalling EVO strollers because an opening between the grab bar and seat can allow an infant's body to pass through, posing a strangulation hazard.

    Product
    EVO strollers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·13V044000·2013-02-07

    BMW Recalls 516,791 Vehicles for Battery Cable Connector Defect

    BMW is recalling 516,791 vehicles from 2007-2012 because a battery cable connector may degrade, causing loss of electrical power and unexpected stalling.

    Product
    BMW — BMW 328I, 335I, 128I, 135I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0964-2013·2013-02-06

    Dymatize Elite Fudge Brownie Protein Bar Recalled for Peanut Allergen

    Belmont Confections is recalling Dymatize Elite Gourmet Fudge Brownie protein bars because a consumer reported an allergic reaction to peanuts.

    Product
    DYMATIZE NUTRITION ELITE Gourmet Fudge Brownie 6-LAYER HI-PROTEIN BAR Label reads in part "NET WT***INGREDIENTS: Elite Protein Blend***Distributed by: Dymatize Enterprises, Inc. 13737 N. Stemmons FWY, Dallas, TX 75234, (888) 334-LEAN or (972) 732-1990.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Drugs)·D-138-2013·2013-02-06

    Qualitest Recalls Hydrocodone and Acetaminophen Tablets Due to Oversized Size

    Qualitest Pharmaceuticals is recalling 897,379 bottles of Hydrocodone bitartrate and acetaminophen tablets because a complaint reported the tablets were oversized.

    Product
    Hydrocodone bitartrate and acetaminophen Tablets, USP, 10 mg/500 mg, packaged in a) 30-count bottles, NDC 0603-3888-16; b) 60-count bottles, NDC 0603-3888-20; c) 90-count bottles, NDC 0603-3888-02; d) 100-count bottles, NDC 0603-3888-21; e) 120-count bottles, NDC 0603-3888-22; f)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0961-2013·2013-02-06

    Knott's Chicken Salad Recalled Due to Listeria Monocytogenes Contamination

    Knott's Wholesale Foods is recalling chicken salad sandwiches because a sample tested positive for Listeria Monocytogenes. The product was distributed in Tennessee and Kentucky.

    Product
    Knott's FINE FOODS, CHICKEN SALAD (sandwich), KNOTT's WHOLESALE FOODS, INC. 125 North Blakemore, Paris, TENNESSEE 38242, (731) 642-1961 www.knotsfoods.com, UPC 011984011326
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0960-2013·2013-02-06

    United Natural Foods Recalls Kinnikinnick Pie Crust Due to Allergy Alert

    United Natural Foods is recalling Kinnikinnick Pie Crust in six states due to an expanded allergy alert issued by the manufacturer.

    Product
    Kinnikinnick Pie Crust (frozen), Weight: 290 g/10 oz, Qty/Pkg: 2, Product packaged in a cardboard box with printed label. UPC: 62013300600 9
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0944-2013·2013-02-06

    Island Delights Coconut Haystack Candy Recalled for Missing Milk Labeling

    Island Delights is recalling Coconut Haystack Candy because the ingredient list failed to disclose milk. The product was distributed to 14 states.

    Product
    Island Delights Coconut Haystack Candy Maple Natural Flavor Coconut Haystacks, NET WEIGHT 2 OZ, 4 oz and 8 oz clear plastic bags. Bags labeled in part "INGREDIENTS: SUGAR, COCONUT***NATURAL MAPLE FLAVOR***Island Delights, Inc. Seville, OH 44273"
    Category
    Food
    Distribution
    14 states
  • SevereFDA (Food)·F-0948-2013·2013-02-06

    Kinnikinnick Frozen Pie Crusts Recalled for Undeclared Egg Allergen

    Jerusalem Manufacturing Natural Foods & Wholesalers, Inc. is recalling Kinnikinnick Foods Brand Frozen Pie Crusts because egg is not declared on the label.

    Product
    Kinnikinnick Foods Brand Frozen Pie Crusts, 290g/10 ounces. 2 crusts per box, 6 boxes per case
    Category
    Food
    Distribution
    0 states
  • SevereNHTSA·13V038000·2013-02-06

    Chrysler Recalls Trucks Due to Rear Axle Pinion Nut Loosening Risk

    Chrysler is recalling specific 2009-2012 Ram 1500, Dodge Dakota, Durango, and Chrysler Aspen trucks because the rear axle pinion nut may loosen, potentially causing a loss of vehicle control.

    Product
    DODGE — DODGE, CHRYSLER DAKOTA, RAM 1500, DURANGO, ASPEN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0754-2013·2013-02-06

    GE AdvantageSim MD Software Recall for Incorrect Series Labeling

    GE Healthcare is recalling AdvantageSim MD versions 7.4 through 7.6 because incorrect series labeling may lead to under-treatment of tumors.

    Product
    AdvantageSim MD versions 7.4 through 7.6, Model 5160092-2 Version 7.4, 5160092-3 Version 7.5, 5160092-4 version 7.6.
    Category
    Medical Device
    Distribution
    13 states
  • SevereFDA (Food)·F-0963-2013·2013-02-06

    Dymatize Elite Protein Bars Recalled for Peanut Allergen Mislabeling

    Belmont Confections is recalling Dymatize Elite Gourmet Cookies & Cream protein bars because they contain peanuts but do not list them on the label.

    Product
    DYMATIZE NUTRITION ELITE Gourmet Cookies & Cream 6-LAYER HI-PROTEIN BAR Label reads in part "NET WT***INGREDIENTS: Elite Protein Blend***Distributed by: Dymatize Enterprises, Inc. 13737 N. Stemmons FWY, Dallas, TX 75234, (888) 334-LEAN or (972) 732-1990.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0943-2013·2013-02-06

    Kinnikinnick Frozen Pie Crust Recalled for Allergen Alert

    Kinnikinnick Foods recalled frozen pie crusts distributed by KeHE Distributors in Minnesota and Pennsylvania due to an allergen alert.

    Product
    Kinnikinnick Pie Crust (frozen) Weight: 290 g/10 oz Qty/Pkg: 2 UPC: 62013300600 9
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0516-2013·2013-02-06

    Motorola Laser Utility Products Recalled for Incorrect Laser Power Settings

    Motorola Inc is recalling PCS3000/CS3070 laser utility products because they were manufactured with Class 2 laser power settings instead of the specified Class 1 levels.

    Product
    Motorola Solutions PCS3000/CS3070 Laser Utility/Peripheral Laser Products
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0762-2013·2013-02-06

    Roche COBAS TaqMan MTB Test Definition Files Recalled for False Negative Risk

    Roche is recalling COBAS TaqMan MTB Test Definition Files due to an incorrect cutoff value that may cause false negative results for tuberculosis tests.

    Product
    COBAS TaqMan Mycobacteria tuberculosis (MTB) Test FOR IN VITRO DIAGNOSTIC USE.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0962-2013·2013-02-06

    C H S Inc Recalls Imitation Bacon Bits Due to Missing Ingredient Labeling

    C H S Inc is recalling Kitchen Essentials Imitation Bacon Flavored Bits because the packaging is missing the ingredient statement for soy and wheat.

    Product
    Kitchen Essentials Imitation Bacon Flavored Bits, contains soy and wheat, packaged in 10 lb bulk cartons. Distributed by Gordon Food Service, Grand Rapids, MI. UPC 0 00 93901 6, Supplier item 293628
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0937-2013·2013-02-06

    EonNutra Recalls SOTO GFC 200 Dietary Supplement Due to Bacterial Contamination

    EonNutra, LLC is recalling SOTO Supplements GFC 200 dietary supplements because the products may be contaminated with various types of bacteria.

    Product
    Growth Factor Complex 200 GFC 200, Dietary Supplement 2 Fl Oz, Manufactured for: Soto Supplements P.O. Box 75774 Colorado Springs, CO 80237, Instructions: Place drops under your tongue for 2 min then swallow. Do not eat or drink for 15 min. Only approved for distribution from Au
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0759-2013·2013-02-06

    Varian Medical Rectal Retractors Recalled for Contamination Risk

    Varian Medical Systems is recalling stainless steel rectal retractors used in brachytherapy due to potential contamination that could cause infections, toxicity, or allergic reactions.

    Product
    Rectal Retractors, stainless steel, item # AL07289000, a component of Varian Medical Ring and Tandem Applicator Sets; Intended for use in Brachytherapy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0940-2013·2013-02-06

    Chocolate Decadence Coconut Balls Recalled for Peanut Cross-Contamination

    Chocolate Decadence is recalling Chocolate Covered Coconut Balls due to a potential peanut cross-contamination hazard. The product was dipped in chocolate previously used for peanut butter items.

    Product
    Chocolate Covered Coconut Balls is packaged in either 2-ounce packages (2 pieces per package) or in 0.5 lb and 1 lb. boxes. The 2-ounce package has a UPC 19815 90007 8. There is no UPC for 0.5 lb. and 1 lb. packages. The product is labeled in parts: "***Chocolate Covered
    Category
    Food
    Distribution
    16 states
  • HighFDA (Food)·F-0953-2013·2013-02-06

    Dawn's Foods Recalls Ocean Harbor Smoked Salmon Spread Due to Pathogen Risk

    Dawn's Foods is voluntarily recalling Ocean Harbor Smoked Salmon Spread in 5 lb and 10 oz containers because the packaging may allow pathogen growth.

    Product
    Ocean Harbor Smoked Salmon Spread Net Wt 5 lb.(2.27 kg). UPC: 0 32345-77707 1 Dist by Roundy's Inc.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0752-2013·2013-02-06

    Extremity Medical Recalls IO FiX System Screw Measuring Device

    Extremity Medical LLC is recalling 93 units of the IO FiX System Accessory screw measuring device because it may measure screw length approximately 5 mm short, potentially leading to the selection of an inappropriate implant size.

    Product
    Extremity Medical, IO FiX System Accessory. Catalog Number 101-00010. This screw measuring device is an accessory to the IO FiX Screw and Washer System that is used to measure the length of the screw by placing the depth gauge over the guidewire and down to the bone. Orthop
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0757-2013·2013-02-06

    Abbott Vascular Recalls RX Accunet Embolic Protection System Lots

    Abbott Vascular is recalling specific lots of the RX Accunet Embolic Protection System because the peel-away sheath may be difficult to remove due to higher than normal wall thickness.

    Product
    Brand Name: RX Accunet Embolic Protection System Common Name: RX Accunet EPS. Part Numbers: 101649-45, 1011649-55, 1011649-65, 1011649-75, 1011650-55, 1011650-65, 1011651-45, 1011651-55. The RX Accunet EPS is indicated for use as a guide wire and embolic protection system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0741-2013·2013-02-06

    Hamilton T1 Ventilator Recall for Pediatric Software Calculation Error

    Hamilton Medical Inc is recalling 97 Hamilton T1 ventilators with software versions 1.1.2 or lower due to a calculation error affecting oxygen consumption estimates for small pediatric patients.

    Product
    HAMILTON-T1 Ventilator with software versions 1.1.2 or lower. The HAMILTON T-1 Ventilator is intended to provide positive pressure ventilatory support to adults and pediatrics
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0947-2013·2013-02-06

    Island Delights Coconut Haystacks Recalled for Missing Milk Allergen Labeling

    Island Delights is recalling specific lots of Almond Natural Flavor Coconut Haystacks because the ingredient list failed to disclose the presence of milk.

    Product
    Island Delights ALMOND Natural Flavor Coconut Haystacks, NET WEIGHT 2 oz, 4 oz, 8 oz and 2 lb clear plastic bags. Bags labeled in part "INGREDIENTS: SUGAR, COCONUT***COCOA***NATURAL COFFEE FLAVOR***Island Delights, Inc., Seville, OH 44273"
    Category
    Food
    Distribution
    14 states
  • HighNHTSA·13V040000·2013-02-06

    Chrysler Recalls 2003-2004 Dodge Vipers Due to Airbag Defect

    Chrysler is recalling 2003 and 2004 Dodge Vipers because a faulty airbag control module component may cause airbags or seatbelt pretensioners to deploy unexpectedly.

    Product
    DODGE — DODGE VIPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0946-2013·2013-02-06

    Island Delights Coconut Haystacks Recalled for Undeclared Milk Allergen

    Island Delights is recalling Coconut Haystacks because the ingredient list fails to declare milk, a major food allergen.

    Product
    Island Delights COFFEE NATURAL Natural Flavor Coconut Haystacks, NET WEIGHT 2 oz, 4 oz, 8 oz and 2 lb clear plastic bags. Bags labeled in part "INGREDIENTS: SUGAR, COCONUT***COCOA***NATURAL COFFEE FLAVOR***Island Delights, Inc. Seville, OH 44273"
    Category
    Food
    Distribution
    14 states
  • HighFDA (Food)·F-0959-2013·2013-02-06

    Dawn's Foods Recalls Alaskan Krab Salad Due to Pathogen Risk

    Dawn's Foods is voluntarily recalling Alaskan Krab Salad in 5 lb and 10 oz containers because the packaging may allow pathogen growth.

    Product
    Dawns Alaskan Krab Salad NET WT 5 LBS (2.27 kg), UPC: 0 32345 85072 9 , MFG BY DAWN'S FOODS, IN., PORTAGE, WI 53901 Ocean Harbor Alaskan Krab Salad NET WT 5 LBS (2.27 kg), UPC: 0 32345 77705 7, Dist by Roundy's Inc.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0740-2013·2013-02-06

    Cordis ExoSeal Vascular Closure Device Recalled for Sterility Assurance Failure

    Cordis is recalling ExoSeal Vascular Closure Devices because the sterilization process did not meet required sterility assurance levels.

    Product
    Cordis, a Johnson and Johnson Company, ExoSeal(TM) 6F Vascular Closure Device, cat. No EX500, EX600, and EX700. Used for femoral artery puncture site closure, reducing times to hemostasis and ambulation in patients who have undergone diagnostic or interventional procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·13115·2013-02-06

    4moms Play Yard Sheets Recalled Due to Entrapment Hazard

    4moms recalled breeze Cotton Jersey Playard Sheets because they are too small for the play yards, posing an entrapment hazard that could lead to suffocation.

    Product
    4moms® breeze™ Cotton Jersey Playard Sheets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0955-2013·2013-02-06

    Dawn's Foods Recalls Ocean Harbor Jalapeno Krab Spread Due to Pathogen Risk

    Dawn's Foods is voluntarily recalling Ocean Harbor Jalapeno Krab Spread in 5 lb and 10 oz containers because the packaging may allow pathogen growth.

    Product
    Ocean Harbor Jalapeno Krab Spread Net Wt 5 lbs (2.27kg) UPC: 0 32345-77715 6 Dist by Roundy's Inc.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0942-2013·2013-02-06

    Food Club Chocolate Chunk Brownie Mix Recalled for Undeclared Walnuts

    Gilster-Mary Lee Corp. is recalling Food Club Chocolate Chunk Brownie Mix because it contains walnuts that are not listed on the ingredient label.

    Product
    Food Club Chocolate Chunk Brownie Mix, packaged in 21.5-oz. boxes, UPC# 36800-13486, distributed by TOPCO Associates LLC, Skokie, IL.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0954-2013·2013-02-06

    Dawn's Foods Recalls Ocean Harbor Cajun Krab Spread Due to Pathogen Risk

    Dawn's Foods is voluntarily recalling Ocean Harbor Cajun Krab Spread in 5 lb and 10 oz containers because the packaging may allow pathogen growth.

    Product
    Ocean Harbor Cajun Krab Spread Net Wt 5 lb (2.27 kg) UPC: 0 32345-77711 8 Dist by Roundy's Inc.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Drugs)·D-140-2013·2013-02-06

    Hillyard Hand Sanitizer Recalled for Potential Bacterial Contamination

    Hillyard GMP is recalling specific lots of Alcohol Free Foaming Instant Hand Sanitizer due to potential bacterial contamination.

    Product
    HILLYARD ALCOHOL FREE FOAMING INSTANT HAND SANITIZER — HILLYARD ALCOHOL FREE FOAMING INSTANT HAND SANITIZER (BENZALKONIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0958-2013·2013-02-06

    Dawn's Foods Recalls Alaskan Krab and Shrimp Salad Due to Pathogen Risk

    Dawn's Foods is voluntarily recalling specific 5-pound and 10-ounce containers of Alaskan Krab and Shrimp Salad because the packaging may allow pathogen growth.

    Product
    Dawns Alaskan Krab and Shrimp Salad NET WT 5 LBS (2.27 kg), UPC: 0 32345 70103 8 MFG BY DAWN'S FOODS, INC., PORTAGE, WI 53901 Ocean Harbor Krab and Shrimp Salad NET WT 5 LBS (2.27 kg), UPC: 0 32345 77701 9 Dist by Roundy's Inc.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0945-2013·2013-02-06

    Island Delights Coconut Haystacks Recalled for Missing Milk Allergen Labeling

    Island Delights, Inc. is recalling specific lots of Coconut Haystacks because the ingredient list failed to disclose milk, a major food allergen.

    Product
    Island Delights Almond Chocolate/Almond Mix Natural Flavor Coconut Haystacks, NET WEIGHT 2 oz, 4 oz, 8 oz and 2 lb clear plastic bags. Bags labeled in part "INGREDIENTS: SUGAR, COCONUT***COCOA***NATURAL ALMOND FLAVOR***Island Delights, Inc., Seville, OH 44273"
    Category
    Food
    Distribution
    14 states
  • HighFDA (Food)·F-0957-2013·2013-02-06

    Dawn's Foods Recalls Cajun Krab Dip Due to Pathogen Risk

    Dawn's Foods, Inc. is voluntarily recalling specific sizes of Cajun Krab Dip because the packaging may allow pathogen growth.

    Product
    Five Star Dip Cajun Krab Dip Net Wt 10 oz (284g). UPC: 0 32345 84063 8, Mfg By Dawns Foods, Inc., Portage, WI 53901. 84080 Dawns Cajun Krab Dip NET WT 5 LBS (2.27 kg), UPC: 0 32345 88888 3 MFG BY DAWN'S FOODS, INC., PORTAGE, WI 53901
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0949-2013·2013-02-06

    Kinnikinnick Pie Crusts Recalled for Undeclared Egg Allergen

    Unified Grocers is recalling Kinnikinnick Pie Crusts because they contain undeclared egg allergen.

    Product
    Kinnikinnick Foods Pie Crusts, 10.2 oz, Item code: 21-35265, UPC 6-20133-00600.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0956-2013·2013-02-06

    Dawn's Foods Recalls Smoked Salmon Dip Due to Pathogen Risk

    Dawn's Foods is voluntarily recalling 5 lb and 10 oz smoked salmon dip products because the packaging may allow pathogen growth.

    Product
    Five Star Dip Smoked Salmon Dip Net WT 10 oz (284g). UPC: 0 32345 61463 5 Mfg By Dawn Food, Portage, WI 53901. Dawns Smoked Salmon Dip NET WT 5 LBS (2.27 kg) UPC: 0 32345 61480 2 MFG BY DAWN'S FOODS, INC., PORTAGE, WI 53901
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0760-2013·2013-02-06

    Varian Medical Systems Recalls Titanium Rectal Retractors for Brachytherapy

    Varian Medical Systems is recalling 152 titanium rectal retractors used in brachytherapy due to potential contamination risks that could cause infections, toxicity, or allergic reactions.

    Product
    Rectal Retractors, titanium, item # AL07368000, a component of Varian Medical Ring and Tandem Applicator Sets; Intended for use in Brachytherapy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0758-2013·2013-02-06

    Ethicon ENSEAL G2 Tissue Sealers Recalled for Potential Self-Activation

    Ethicon Endo-Surgery Inc. is recalling ENSEAL G2 Tissue Sealers because they may self-activate during use, causing unintended thermal damage.

    Product
    Ethicon Endo-Surgery Inc. The ENSEAL¿ G2 Tissue Sealers are indicated for bipolar coagulation and mechanical transection of tissue during laparoscopic and open procedures. Model Numbers: NSLG2C14 NSLG2C25 NSLG2C35 NSLG2C45 NSLG2514 NSLG2S25 NSLG2S35 NSLGS545
    Category
    Medical Device
    Distribution
    46 states
  • HighFDA (Devices)·Z-0756-2013·2013-02-06

    BD Vacutainer Citrate Blood Collection Tubes Recalled for Test Errors

    Becton Dickinson is recalling specific blood collection tubes due to reports of extended Partial Thromboplastin Time (aPTT) test results.

    Product
    BD Vacutainer Buffered Sodium Citrate (9NC) Plus Blood Collection Tubes; Sterile; IVD; REF 363083; 13 X 75 mm, 2.7 mL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0941-2013·2013-02-06

    Jiffy Food Service Recalls Spice Cake Mix for Undeclared Milk Allergen

    Jiffy Food Service is voluntarily recalling 25 lb. and 50 lb. bags of Spice Cake Mix due to an undeclared milk allergen. The product was distributed to correctional facilities nationwide.

    Product
    Spice Cake Mix , 25 lb. and 50 lb. kraft bags, labelled a) CMC Quality and Value, Spice Cake Mix, 46702-00985, NET Wt. 25 lbs. (11.34 kg) JIFFY Foodservice, LLC, Chelsea, Michigan 48188; b) CMC Quality and Value, Spice Cake Mix, 46702-00920, NET Wt. 50 lbs. (22.68 kg.), JIFFY Foo
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0742-2013·2013-02-06

    Mindray Recalls DPM5 Monitors Due to Missing ST and Arrhythmia Features

    Mindray is recalling 13 DPM5 vital signs monitors because ST and Arrhythmia features may not be available.

    Product
    Mindray DPM5 Monitor, a vital signs monitor used on human patients in healthcare facilities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0751-2013·2013-02-06

    Greatbatch Medical Recalls 45 Degree Angle Drivers for Noisy Operation

    Greatbatch Medical is voluntarily recalling 913 Small Angled Driver 45 units worldwide due to reports of noisy or rough operation.

    Product
    45¿ Angle Driver / Z-H, Greatbatch Medical 10 000 Wahrie Drive, Clarance, NY 14031. Model #: P2661, P2662, T3635, T5586,T6031, T6164,T10161, T12628,T14879, T16422,T2487,T2713,T116057, T13635, MPU260045AO01, MPU260045ZH01. The Driver is intended to act as an interface betw
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-0750-2013·2013-02-06

    Envoy Medical Recalls Esteem Programmers for Noise Interference

    Envoy Medical is voluntarily correcting 44 Esteem Programmers to reduce susceptibility to noise interference.

    Product
    Esteem Programmer Model 6001, US and ISA, Model 3001 Dell E54XX, part of the Esteem Totally Implantable Hearing System. The ISA and Commander are software packages that run on a laptop personal computer.
    Category
    Medical Device
    Distribution
    14 states
  • ModerateFDA (Devices)·Z-0743-2013·2013-02-06

    Alfa Wassermann System Diluent Recalled for Inaccurate Calibration Results

    Alfa Wassermann is recalling 4,104 kits of System Diluent because inorganic phosphorus assays may not produce acceptable calibration results.

    Product
    Alfa Wassermann System Diluent 750 mL Manufactured for Alfa Wassermann Diagnostic Technologies LLC 4 Henderson Drive West Caldwell, NJ 07006 Alfa Wassermann B.V. Pompmolenlaan 24 3447 GK, Woerden The Netherlands Common name is water solution. Intended to dilute reagent
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0739-2013·2013-02-06

    Becton Dickinson Recalls BBL Fildes Enrichment Tubes for Growth Failure

    Becton Dickinson is recalling BBL Fildes Enrichment tubes because they may fail to support the growth of Haemophilus species, potentially affecting laboratory test results.

    Product
    BBL(TM) Fildes Enrichment, catalog number 211866, 10 tubes/pack, labeled in part ***Becton Dickinson and Company, Sparks, MD 21152 USA*** Intended Use: Fildes Enrichment may be used to enrich a variety of media for the cultivation of various microorganisms. Fildes Enrichment i
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0951-2013·2013-02-06

    JFC International Recalls Saki Ika Cuttlefish Due to Mold Contamination

    JFC International is recalling specific lots of WelPac Saki Ika Cuttlefish because of mold. Consumers should check their products and stop using them if they match the listed codes.

    Product
    WP Saki Ika Cuttlefish Hot JFC# 15606, 4/24/0.75 oz; JFC# 06318, 8/12/2 oz; JFC# 07269, 5/12/4 oz; JFC# 06360, 3/12/8 oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0952-2013·2013-02-06

    Gordon Food Service Recalls Pasteurized Crab Meat Due to Temperature Abuse

    Gordon Food Service is recalling 10 cases of 16-ounce pasteurized crab meat sold in Florida due to time and temperature abuse during transit.

    Product
    ***GFS***CLAW MEAT***Wild-Caught and Hand-Picked***PASTEURIZED CRAB***Carne de mano de jaiba*** NET WT/PESO NETO***16 OZ (1 LB) 453g***Reorder #536030***PRODUCT OF THAILAND***.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0702-2013·2013-02-06

    Philips Juno DRF X-ray System Recalled for Display Compliance Issues

    Philips Healthcare is recalling 16 Juno DRF X-ray systems because fluoroscopy dose values may not display correctly at the operator's position.

    Product
    Juno DRF , X-ray system, diagnostic, Fluoroscopic, general-purpose Model: 70920 Product Usage: Universal R/F, general use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0938-2013·2013-02-06

    The Father's Table Vanilla Rolls Recalled for Missing Allergen Labeling

    The Father's Table LLC is recalling Vanilla Rolls because the labels fail to list strawberries and color additives. The FDA classified this as a Class III recall.

    Product
    Individual packages labeled in part: ***The Father's Table***Vanilla Roll***8oz**** and Master carton labeled in part: "The Father's Table***Shelf Stable*** Mini Vanilla Roll***Contains 12/8oz.***
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Devices)·Z-0755-2013·2013-02-06

    Ortho VITROS Vapor Adsorption Cartridges Recalled for Incorrect Packaging

    Ortho-Clinical Diagnostics is recalling VITROS Vapor Adsorption Cartridges because some cartons incorrectly contain Particulate Cartridges, which may bias test results.

    Product
    Ortho Clinical Diagnostics VITROS¿ Chemistry Products Vapor Adsorption Cartridge REF/CAT No. 680 0100. VITROS¿ Vapor Adsorption Cartridges are used to remove vapor contaminants that may potentially interfere with Signal Reagent used with MicroWell Assays on the VITROS¿ 3600, VI
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0936-2013·2013-02-06

    General Mills Recalls Betty Crocker Cake Mix for Undeclared Colors

    General Mills is recalling a limited quantity of Betty Crocker SuperMoist Golden Vanilla cake mix due to a labeling error involving undeclared FD&C color ingredients.

    Product
    Betty Croker, Super Moist Cake Mix, Golden Vanilla, NET WT 15.25 oz (432 g), UPC 0 16000 40993 4, Dist by General Mills Sales, Inc., Minneapolis, MN 55440. Case UPC code 1600040993000
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Food)·F-0950-2013·2013-02-06

    JFC International Recalls Saki Ika Cuttlefish Due to Mold Contamination

    JFC International is recalling specific lots of Saki Ika Cuttlefish nationwide because of mold. Consumers should check their products and discard any affected items.

    Product
    WP Saki Ika Cuttlefish JFC# 15603, 4/24/0.75oz; JFC# 06315, 8/12/2oz; JFC# 07266, 5/12/4oz; JFC# 06375, 3/12/8oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0939-2013·2013-02-06

    The Father's Table Recalls Vanilla Mini Cake Rolls for Labeling Errors

    The Father's Table, LLC is recalling Vanilla Mini Cake Rolls because the labels fail to list strawberries and specific color additives.

    Product
    Individual packages labeled in part: ***The Bakery baked with pride***Vanilla Mini Cake Roll***8oz**** with strawberry filling*** NETWT 8oz (226g)
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Devices)·Z-0738-2013·2013-02-06

    bioMerieux Recalls BacT/ALERT SA Blood Culture Bottles with Uncured Sensors

    bioMerieux, Inc. is recalling BacT/ALERT SA Blood Culture Bottles because some units may contain uncured sensors, potentially affecting the detection of microorganisms.

    Product
    BacT/ALERT SA Blood Culture Bottle. The BacT/ALERT SA reagent bottle is intended to be recover and detect aerobic microorganisms (bacteria and fungi) from blood and other normally sterile body fluids.
    Category
    Medical Device
    Distribution
    29 states
  • ModerateFDA (Drugs)·D-139-2013·2013-02-06

    Schering-Plough Recalls Temodar Capsules Due to Degradation Testing Failures

    Schering-Plough is recalling 17,169 packages of Temodar (temozolomide) 20 mg capsules due to out-of-specification degradation product testing results.

    Product
    Temodar (temozolomide) Capsule, 20 mg per capsule, 5 capsules per package, For Oral Administration, Rx Only, Cytotoxic, NDC: 0085-1519-02, Schering Corporation, Kenilworth, New Jersey, 07033
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-137-2013·2013-02-06

    Mylan Recalls Carvedilol Tablets for Weight and Thickness Failures

    Mylan Pharmaceuticals is recalling 11,580 bottles of Carvedilol 12.5 mg tablets because they failed specifications for weight and thickness.

    Product
    Carvedilol Tablets, USP, 12.5 mg, 500-count tablets per bottle, Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A., NDC 0378-3633-05, UPC 3 0378-3633-05 3.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-141-12013·2013-02-06

    Femtrace Tablets Recalled for Moisture Ingress and Impurity Failures

    Warner Chilcott is recalling 5,439 bottles of Femtrace 0.9 mg tablets nationwide due to moisture ingress causing failed impurity specifications.

    Product
    Femtrace 0.9 mg (Estradiol Acetate) Tablets, Rx Only, 100 tablets, Manufactured by Pharmaceutics International Inc, Hunt Valley, MD 21031 for Warner Chilcott Company LLC, Fajardo, PR 00738
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0764-2013·2013-02-06

    MOOG Infinity Enteralite Feeding Pumps Recall for Manual Addendum

    MOOG Medical Devices Group is recalling 92,488 Infinity Enteralite Ambulatory Feeding Pumps to add an operator's manual addendum regarding the Infinite Dose mode and air-in-line detection limitations.

    Product
    Infinity Enteralite Ambulatory Feeding Pumps, List number: INFKIT2 - Addendum to Operator's Manual Product usage: provide a means for the volumetric delivery of fluids used in Enteral applications.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0753-2013·2013-02-06

    Biomet TUNNELOC Round Head Interference Screw Recalled for Undersized Tip Hole

    Biomet is recalling 44 TUNNELOC Round Head Interference Screws because the hole at the tip is undersized. The defect may affect the device's performance during orthopedic procedures.

    Product
    TUNNELOC ROUND HEAD INTERFERENCE SCREW 8MMX25MM Biomet Sports Medicine manufactures a variety of internal fixation devices intended to aid in arthroscopic and orthopedic reconstructive procedures requiring soft tissue fixation, due to injury or degenerative disease. Implants us
    Category
    Medical Device
    Distribution
    7 states
  • LowFDA (Devices)·Z-0745-2013·2013-02-06

    Siemens Dimension IRON Calibrator Recalled for Calibration Slope Issues

    Siemens Healthcare Diagnostics is recalling Dimension IRON Calibrators because some lots produced calibration results outside acceptable ranges.

    Product
    Dimension(R) IRON Calibrator (DC85), Siemens material number 10445010. The Dimension(R) IRON Calibrator is an in vitro diagnostic product intended to be used to calibrate the Iron method for the Dimension(R) clinical chemistry system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-142-2013·2013-02-06

    Femtrace 0.45 mg Tablets Recalled for Moisture Ingress

    Warner Chilcott is recalling 3,155 bottles of Femtrace 0.45 mg tablets due to moisture ingress that failed impurity specifications.

    Product
    Femtrace 0.45 mg (Estradiol Acetate) Tablets, Rx Only, 100 tablets, Manufactured by Pharmaceutics International Inc, Hunt Valley, MD 21031 for Warner Chilcott Company LLC, Fajardo, PR 00738
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0747-2013·2013-02-06

    Alere Cholestech LDX Calibration Verification Recall for HDL Errors

    Alere San Diego, Inc. is recalling 614 kits of Cholestech LDX Calibration Verification due to out-of-range HDL cholesterol results.

    Product
    Alere Cholestech LDX Calibration Verification, 4 vial set, Catalog Number: 88770 Alere Cholestech LDX Calibration Verification (hereafter referred to as CAL VERS) enables users to monitor the performance of total cholesterol (TC), high density lipoprotein cholesterol (HDL), tr
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0746-2013·2013-02-06

    Alere Cholestech LDX Multianalyte Control Recalled for HDL Errors

    Alere San Diego, Inc. is recalling Alere Cholestech LDX Multianalyte Control kits because they may produce out-of-range HDL cholesterol results.

    Product
    Alere Cholestech LDX Multianalyte Control, 2 vial set, Catalog Number: 88769 Alere Cholestech LDX Multianalyte Control (hereafter referred to as Controls) enables users to monitor the performance of total cholesterol (TC), high density lipoprotein cholesterol (HDL), triglyceri
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·13721·2013-02-05

    Club Car Recalls Precedent Gas-Powered Golf and Transport Vehicles

    Club Car is recalling about 1,450 Precedent gas-powered golf and transport vehicles because the fuel hose could separate from the tank, posing a fire hazard.

    Product
    Precedent golf and transport vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V035000·2013-02-04

    Yamaha Recalls 2009 Zuma 125 Scooters for Fuel Pump Defect

    Yamaha is recalling 2009 Zuma 125 scooters because a fuel pump defect may cause engine stalling, increasing crash risk.

    Product
    YAMAHA — YAMAHA redundant ZUMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V037000·2013-02-01

    Forest River Recalls 2013 Motor Homes Due to Ignition Key Defect

    Forest River is recalling 2013 Concord, Leprechaun, Freelander, Lexington, Forester, and Sunseeker motor homes because the ignition key may be removed while the vehicle is running.

    Product
    FOREST RIVER — FOREST RIVER LEXINGTON, FREELANDER, LEPRECHAUN, CONCORD
    Category
    Vehicle
    Distribution
    Distributed nationwide

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