The Recall Desk

Archive

December 2018 recalls

451 recalls were announced in December 2018.

What the numbers show

Critical
15
Severe
134
High
189
Moderate
96
Low
17

Of the 451 recalls this month scored against our rubric, 3% are Critical, 30% are Severe.

Which agencies issued them

401–451 of 451

  • HighFDA (Food)·F-0666-2019·2018-12-05

    Thatchers Gingerbread Popcorn Recalled for Undeclared Wheat Allergen

    Thatchers is recalling 2,898 units of 8-ounce Gingerbread Popcorn sold at Disney locations because the ingredient list declares flour but fails to declare wheat.

    Product
    Gingerbread Popcorn. 8 ounce (227 grams) flexible plastic bag. Brand name of Disney Theme Park Merchandise or Disney Parks Distributed by Disney Theme Park Merchandise Lake Buena Vista, FL 32830 UPC Code 400020873569
    Category
    Food
    Distribution
    4 states
  • HighFDA (Drugs)·D-0285-2019·2018-12-05

    Germ Bloc Health Hand Sanitizer Foam Recalled for Pseudomonas Contamination

    AVKARE Inc. is recalling specific lots of Germ Bloc Health Hand Sanitizer Foam due to the presence of Pseudomonas aeruginosa.

    Product
    Germ Bloc Health Hand Sanitizer Foam (benzalkonium chloride 0.13%) 7.5fl.oz./222mL refill bags, AvKARE, Inc. Pulaski, TN 38478 www.avkare.com, NDC 5026835427, UPC 3 50268 35408
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Food)·F-0720-2019·2018-12-05

    Chukar Cherry Company Recalls Ultra Dark Chocolate Amaretto Rainier Cherries

    Chukar Cherry Company is recalling Ultra Dark Chocolate Amaretto Rainier Cherries because the product contains milk, which is not listed on the label.

    Product
    Ultra Dark Chocolate Amaretto Rainier Cherries, Chukar Cherries brand, packaged in 7.5 oz. plastic pouches. UPC 0 11261 22307 7.
    Category
    Food
    Distribution
    22 states
  • HighFDA (Devices)·Z-0436-2019·2018-12-05

    Maquet QUADROX-i Neonatal Membrane Oxygenator Recalled for Blood Leakage Risk

    Maquet is recalling QUADROX-i Neonatal membrane oxygenators because a specific reducing screw adapter may cause blood leakage at the inlet connector.

    Product
    QUADROX-i Neonatal without integrated arterial filter and VHK 11000 (VKMO 10000-USA#QUADROX-i Neo.+Reservoir), Part Number 701055120 The membrane oxygenator QUADROXi Neonatal is intended for use in extracorporeal circulation during cardiopulmonary bypass in cardiac surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0524-2019·2018-12-05

    GE Healthcare Recalls Solar 9500 Patient Monitors Due to Network Overload Risk

    GE Healthcare is recalling approximately 3,864 Solar 9500 Information Monitoring Systems because they may simultaneously restart if connected to the same network during a prolonged network overload.

    Product
    Solar 9500 Information Monitoring System is used to monitor physiologic parameter data on adult, pediatric and neonatal patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0520-2019·2018-12-05

    GE Healthcare Recalls Dash 4000 Patient Monitoring Systems

    GE Healthcare is recalling Dash 4000 Patient Monitoring Systems because they may simultaneously restart if connected to the same network during a prolonged network overload.

    Product
    Dash 4000 Patient Monitoring System is used to monitor physiologic parameter data on adult, pediatric and neonatal patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0675-2019·2018-12-05

    Duncan Hines Classic Yellow Cake Mix Recalled for Salmonella

    ConAgra Foods is recalling Duncan Hines Classic Yellow cake mix after a positive finding of Salmonella in a retail sample.

    Product
    Duncan Hines Classic Classic Yellow cake mix 15.25oz. 12 retail units per case 644209307494
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0672-2019·2018-12-05

    Finax Muesli Recalled for Missing Coconut Allergen Labeling

    Chicago Importing Co is recalling Finax Muesli with 45% Fruit because the ingredients statement does not indicate the presence of coconut.

    Product
    Finax Muesli with 45% Fruit; 22.9-oz.; Heat sealed plastic bag; 10 bags/case
    Category
    Food
    Distribution
    12 states
  • HighFDA (Devices)·Z-0504-2019·2018-12-05

    NxStage PureFlow B Solution Recalled for Potential Bag Burst Injury Risk

    NxStage Medical is recalling PureFlow B Solution because the smaller chamber of the two-chamber bag can burst, releasing electrolyte fluid that may cause injury if it contacts eyes or skin.

    Product
    NxStage PureFlow B Solution-RFP-404, Premixed Dialysate for Hemodialysis NxStage PureFlow B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0670-2019·2018-12-05

    Shirleys Chocolate Whoopie Pies Recalled for Undeclared Peanut Allergen

    Shirleys Cookie Company is recalling Chocolate Peanut Butter Whoopie Pies labeled as Chocolate Whoopie Pies because the peanut allergen is not declared on the packaging.

    Product
    Weis Chocolate Whoopie Pie 16 oz (454g)/ 4 4 oz Whoopie Pies Clamshell Packaging 4 Whoopie Pies per Unit
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0501-2019·2018-12-05

    NxStage PureFlow B Solution Recalled Due to Bag Burst Risk

    NxStage Medical is recalling PureFlow B Solution because the smaller chamber of the two-chamber bag can burst, releasing electrolyte fluid that may injure eyes or skin.

    Product
    NxStage PureFlow B Solution-RFP-401, Premixed Dialysate for Hemodialysis NxStage PureFlow B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0503-2019·2018-12-05

    NxStage PureFlow B Solution Recalled Due to Bag Burst Risk

    NxStage Medical is recalling 2,189 units of PureFlow B Solution because the bag's smaller chamber can burst, releasing electrolyte fluid that may injure eyes or skin.

    Product
    NxStage PureFlow B Solution-RFP-403, Premixed Dialysate for Hemodialysis NxStage PureFlow B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0721-2019·2018-12-05

    Chukar Cherry Company Recalls Ultra Dark Chocolate Black Forest Cherries

    Chukar Cherry Company is recalling Ultra Dark Chocolate Black Forest Cherries due to the unintentional presence of milk, which is not listed on the label.

    Product
    Ultra Dark Chocolate Black Forest Cherries, Chukar Cherries brand, packaged in 7.5 oz. plastic pouches. UPC 0 11261 23907 8. The label is read in parts: "***ULTRA DARK CHOCOLATE BLACK FOREST CHERRIES***Ingredients: Bittersweet Chocolate (Cacao Beans, Pure Cane Sugar, Unsweeten
    Category
    Food
    Distribution
    22 states
  • HighFDA (Devices)·Z-0522-2019·2018-12-05

    GE Healthcare Recalls Solar 8000i Patient Monitoring Systems

    GE Healthcare is recalling approximately 73,673 Solar 8000i and 8000M patient monitoring systems because they may simultaneously restart during prolonged network overloads.

    Product
    Solar 8000i Patient Monitoring System is used to monitor physiologic parameter data on adult, pediatric and neonatal patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0676-2019·2018-12-05

    Duncan Hines Cake Mix Recalled for Salmonella Contamination

    ConAgra Foods is recalling Duncan Hines Classic Butter Golden cake mix due to a positive Salmonella finding in a retail sample.

    Product
    Duncan Hines Classic Butter Golden cake mix 15.25oz. 12 retail units per case 644209307593
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0679-2019·2018-12-05

    Purveyors Kitchen Pumpkin Pesto Tapenade Recalled for Undeclared Walnut Allergen

    Nor Cal Food Solutions LLC is recalling Purveyors Kitchen Pumpkin Pesto Tapenade because the product does not declare walnuts as an ingredient or allergen.

    Product
    Purveyors Kitchen Pumpkin Pesto Tapenade; NET WT 7.75 oz. (220G) UPC: 0 37677 01624 9 Ingredients: Water, Pumpkin, Basil, Parsley, Canola Oil, Sugar, Garlic, Parmesan Cheese (pasteurized skim milk, cultures, salt, enzymes), Lemon juice [concentrate], Sea Salt, Spices. Man
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0512-2019·2018-12-05

    Smiths Medical Recalls Medex High Pressure Stopcocks Due to Leak Risk

    Smiths Medical ASD Inc. is recalling specific lots of Medex High Pressure Stopcocks because an inner body defect may cause the device to leak.

    Product
    Medex High Pressure Stopcock used to control the direction of IV fluid flow. This device is intended for single use only and is provided sterile and fluid path non-pyrogenic unless package is damaged or opened.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0521-2019·2018-12-05

    GE Healthcare Recalls Dash 5000 Patient Monitoring Systems

    GE Healthcare is recalling approximately 182,640 Dash 5000 Patient Monitoring Systems because they may simultaneously restart during prolonged network overloads.

    Product
    Dash 5000 Patient Monitoring System is used to monitor physiologic parameter data on adult, pediatric and neonatal patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0677-2019·2018-12-05

    Duncan Hines Confetti Cake Mix Recalled for Salmonella

    ConAgra Foods is recalling Duncan Hines Signature Confetti Cake Mix after a positive finding of Salmonella in a retail sample.

    Product
    Duncan Hines Signature Confetti Cake cake mix 15.25oz. 12 retail units per case 644209414550
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0668-2019·2018-12-05

    Mary's Harvest Fiesta Corn Salsa Recalled for Potential Contamination

    Mary's Harvest Fresh Foods is recalling 16 oz. Fiesta Corn Salsa due to potential contamination with Salmonella or Listeria monocytogenes.

    Product
    Refrigerated Mary's Harvest Fiesta Corn Salsa 16 oz. UPC# 088724158450, in rigid plastic container
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0719-2019·2018-12-05

    Pictsweet Farms Steam'ables Asparagus Spears Recalled for Listeria

    Hart Freeze pack, LLC is recalling Pictsweet Farms Steam'ables Asparagus Spears because the product tested presumptive positive for Listeria monocytogenes.

    Product
    Pictsweet Farms Steam'ables Asparagus Spears 8oz. pouch, 10 per case UPC 0 70560 97799 9 Frozen
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0500-2019·2018-12-05

    NxStage PureFlow B Solution Recalled for Potential Bag Bursting

    NxStage Medical is recalling 59,100 units of PureFlow B Solution because the smaller chamber may burst, releasing electrolyte fluid that can injure eyes or skin.

    Product
    NxStage PureFlow B Solution-RFP-400, Premixed Dialysate for Hemodialysis. NxStage PureFlow B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0669-2019·2018-12-05

    Kroger Southwest Sweet Potato Rice Recalled for Potential Pathogen Contamination

    Mary's Harvest Fresh Foods is recalling Kroger Southwest Sweet Potato Rice due to potential contamination with Salmonella or Listeria monocytogenes.

    Product
    Refrigerated Kroger Southwest Sweet Potato Rice 12 oz. UPC # 826766185610. In rigid plastic container. Label has cooking instructions which states: Heat vegetable oil until very hot in large saute pan. Toss in vegetable and stir fry 1 minute.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0724-2019·2018-12-05

    Chukar Cherry Company Recalls Organic Chocolate Cherries for Unlabeled Milk

    Chukar Cherry Company is recalling Organic Ultra Dark Orange Chocolate Tart Cherries because the product contains milk, which is not listed on the label.

    Product
    Organic Ultra Dark Orange Chocolate Tart Cherries, Chukar Cherries brand, packaged in 7.5 oz. plastic pouches. UPC 0 11261 27207 5. The label is read in parts: "***ORGANIC ULTRA DARK ORANGE CHOCOLATE TART CHERRIES *** Ingredients: Organic Bittersweet Chocolate (Organic Cacao B
    Category
    Food
    Distribution
    22 states
  • HighNHTSA·18V865000·2018-12-05

    Elgin Street Sweepers Recalled for Air Brake Fitting Failure Risk

    Elgin is recalling 2015-2018 street sweepers because a T-fitting on the air brake system may fail, causing the parking brake to apply unexpectedly and increasing crash risk.

    Product
    ELGIN — ELGIN BROOM BEAR, WHIRLWIND, EAGLE, ROAD WIZARD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0287-2019·2018-12-05

    Ascend Recalls Quetiapine Tablets Due to Metal Shard Contamination

    Ascend Laboratories is recalling Quetiapine 400 mg tablets because a metal shard was found in a tablet. Patients should stop using the affected lot and contact their healthcare provider.

    Product
    QUETIAPINE — QUETIAPINE (QUETIAPINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0519-2019·2018-12-05

    GE Healthcare Recalls Dash 3000 Patient Monitoring Systems

    GE Healthcare is recalling Dash 3000 patient monitors because they may restart simultaneously during prolonged network overloads.

    Product
    Dash 3000 Patient Monitoring System is used to monitor physiologic parameter data on adult, pediatric and neonatal patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0498-2019·2018-12-05

    Stryker Recalls Reprocessed Xcel Bladeless Trocars Due to Distribution Error

    Stryker Sustainability Solutions is recalling 4,848 reprocessed Xcel Bladeless Trocars (H12LP) because they were distributed to facilities after a previous recall was executed.

    Product
    Reprocessed Xcel Bladeless Trocar (H12LP) Model # H12LP Reprocessed Endoscopic Trocars12x100mm - Product Usage: Physical Product Description: The Reprocessed Blunt Tip Trocar consists of a radiolucent cannula and obturator sized 12mm in diameter (refer to Figure 1). The Reprocess
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0513-2019·2018-12-05

    PerkinElmer QSight 210 MD Mass Spectrometer Software Data Overwrite Recall

    PerkinElmer is recalling 18 QSight 210 MD mass spectrometers because a software defect may overwrite original data from the last acquired sample when automatic flush is enabled.

    Product
    PerkinElmer QSight 210 MD Mass Spectrometer Simplicity 3Q MD v1.0 with Hot Fix 2 Software intended to identify compounds in human samples by ionizing the compound and separating the resulting ions. Part Number: BC004872
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0517-2019·2018-12-05

    Fresenius Granuflo Dry Acid Concentrate Recalled for Foreign Substance

    Fresenius Medical Care is recalling specific lots of Granuflo Dry Acid Concentrate for hemodialysis due to the presence of a foreign substance.

    Product
    Fresenius Granuflo Dry Acid Concentrate- 2K 2.5 Ca 1 Mg 16.5 GAL Catalog Number: OFD2251-3B for hemodialysis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0510-2019·2018-12-05

    Numed Multi-Track Angiographic Catheter Recall for Missing Instructions

    Numed Inc is recalling 100 units of Multi-Track Angiographic Catheters because the Instructions for Use booklets were not included on the outer pouch.

    Product
    Multi-Track Angiographic Catheter (MMTA) Product Code: MMTA05100 Product Usage: Recommended for use in catheterization for angiography of cardiovascular vessels and I or chambers. It can be used for injection of contrast medium and pressure measurement in any chamber or vessel
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0509-2019·2018-12-05

    Tosoh AIA-900 Analyzer Recalled for Potential Drive Motor Failure

    Tosoh Bioscience is recalling 247 AIA-900 Automated Immunoassay Analyzers due to a potential drive motor defect that may cause the device to stop functioning and delay patient test results.

    Product
    AIA-900 Automated Immunoassay Analyzer, product code 022930 /022930R Product Usage: The AIA-900 is capable of performing three methods of immunoassay: an immunoenzymetric (IEMA) or sandwich immunoassay, a competitive binding (EIA) immunoassay, and a two-step immunoenzymetric
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1208-2019·2018-12-05

    Akorn Recalls Clindamycin Phosphate Topical Solution Due to Impurity Failures

    Akorn, Inc. is recalling 58,393 jars of Clindamycin Phosphate Topical Solution USP, 1% because the product failed impurity and degradation specifications.

    Product
    Clindamycin Phosphate Topical Solution USP, 1% (10 mg/mL clindamycin), 60 pledget applicators per jar, Rx only. Manufactured by Ei LLC 2865 N. Cannon Blvd. Kannapolis, NC 18083. NDC# 61748-0201-60
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0282-2019·2018-12-05

    Allergan Recalls INFed Iron Dextran Injection for Stability Failure

    Allergan is recalling INFed (Iron Dextran Injection) vials because they failed stability specifications for iron content. The product was distributed throughout the United States.

    Product
    INFed (Iron Dextran Injection USP) 100 mg elemental iron/2 mL (50 mg/mL), Rx only, packaged in 2 mL Sterile Single Dose Vial, Mfd by Patheon Italia S.p.A. Ferentino, Italy NDC 52544-931-07
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0499-2019·2018-12-05

    Siemens Dimension Vista Lactate Dehydrogenase Reagent Cartridge Recall

    Siemens is recalling Dimension Vista Lactate Dehydrogenase reagent cartridges because they may produce falsely elevated results if used after Lactic Acid assays.

    Product
    Dimension Vista Lactate Dehydrogenase (LDI) Flex reagent cartridge, an in vitro diagnostic test for the quantitative measurement of lactate dehydrogenase in human serum and plasma on the Dimension Vista¿ System.Cat. No. K2054, Mat. No. 10464323
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0284-2019·2018-12-05

    RemedyRepack Recalls Nitrofurantoin Capsules Due to Cross-Contamination

    RemedyRepack Inc. is recalling specific lots of Nitrofurantoin Monohydrate/Macrocrystals capsules due to potential cross-contamination with unrelated ingredients.

    Product
    Nitrofurantoin Monohydrate/Macrocrystals capsules,100 mg, packaged in HDPE 60 cc bottles, Rx only, MFG: Sandoz Inc., Princeton, NJ, Repackaged by: RemedyRepack, Indiana, PA, Original NDC 00185-0122-01Repackaged NDC 70518-1087-00, 14 capsules in HDPE 60 cc bottles in cardboard tra
    Category
    Drug
    Distribution
    1 state
  • LowFDA (Devices)·Z-0508-2019·2018-12-05

    WOM World of Medicine Recalls PNEUMOCLEAR Heated High-Flow Tube Sets

    WOM World of Medicine AG is recalling PNEUMOCLEAR Heated High-Flow Tube Sets because packaging may be damaged by the tube set prongs.

    Product
    PNEUMOCLEAR Heated High-Flow Tube Set Product Usage: The Heated High-Flow Tube Set is a single use sterile tube set used in combination with the PNEUMOCLEAR C02 insufflator as a separate accessory. The device PNEUMOCLEAR is a C02 insufflator intended for use during diagnost
    Category
    Medical Device
    Distribution
    1 state
  • LowFDA (Devices)·Z-0516-2019·2018-12-05

    Fresenius Granuflo Dry Acid Concentrate Recalled for Foreign Substance

    Fresenius Medical Care is recalling Granuflo Dry Acid Concentrate for hemodialysis due to confirmed foreign substance contamination.

    Product
    Fresenius Granuflo Dry Acid Concentrate- 2K 2.0 Ca 1 Mg 16.5 GAL Catalog Number: OFD2201-3B for hemodialysis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0511-2019·2018-12-05

    Numed Multi-Track Angiographic Catheter Recall for Missing Instructions

    Numed Inc is recalling 100 units of Multi-Track Angiographic Catheters because Instructions for Use booklets were not included on the outer pouch.

    Product
    Multi-Track Angiographic Catheter (MMTA) Product Code: MMTA06100 Product Usage: Recommended for use in catheterization for angiography of cardiovascular vessels and I or chambers. It can be used for injection of contrast medium and pressure measurement in any chamber or vessel
    Category
    Medical Device
    Distribution
    1 state
  • LowFDA (Food)·F-0671-2019·2018-12-05

    Red Bull Energy Drink Recalled for Excess Ingredient Levels

    Red Bull North America Inc. is recalling specific batches of 8.4 fl. oz. Red Bull Energy Drink because they contain three times the specified level of primary ingredients.

    Product
    Red Bull Energy Drink, 8.4 Fl. oz. (250 mL) Ingredient: Carbonated water, Sucrose, Glucose, Citric Acid, Taurine, Sodium Bicarbonate, Magnesium, Carbonate Caffeine, Nicainamide, Calcium Pantothenate, Pyridoxine HCL, Vitamin B12, Natural and artificial Flavors, colors. UPC
    Category
    Food
    Distribution
    5 states
  • SevereUSDA FSIS·085-2018 EXP·2018-12-04

    JBS Tolleson Recalls Raw Beef Products Due to Salmonella Newport

    JBS Tolleson is recalling approximately 12.1 million pounds of raw beef products, including ground beef, due to possible Salmonella Newport contamination.

    Product
    JBS Tolleson Inc. — JBS Tolleson, Inc. Recalls Raw Beef Products due to Possible Salmonella Newport Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V859000·2018-12-04

    Newmar Recalls 2018-2019 Motorhomes Due to Loose Brake Caliper Bolts

    Newmar is recalling 2018-2019 Essex, Ventana, and London Aire motorhomes because brake caliper mounting bolts may be loose, increasing crash risk.

    Product
    NEWMAR — NEWMAR VENTANA LE, VENTANA, ESSEX, LONDON AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19720·2018-12-04

    Foremost Recalls Glass Shower Doors and Panels Due to Hinge Failure

    Foremost is recalling about 700 glass shower doors and panels because pivot hinges can fail, causing the glass to separate from the frame and fall or shatter.

    Product
    Glass shower doors and panels
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V857000·2018-12-03

    Gulf Stream Vintage Cruiser Recalled for Insufficient Bearing Grease

    Gulf Stream is recalling 2019 Vintage Cruiser recreational trailers because inner hub bearings may lack sufficient grease, risking overheating and hub failure.

    Product
    GULF STREAM — GULF STREAM VINTAGE CRUISER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V858000·2018-12-03

    McNeilus and Oshkosh Trucks Recalled for CNG Valve Defect

    McNeilus is recalling 2016-2018 trucks and Oshkosh S-Series vehicles because a CNG fuel tank valve stem may eject, posing injury and fire risks.

    Product
    MCNEILUS — MCNEILUS, OSHKOSH XE REAR LOADER, STANDARD MIXER, BRIDGEMASTER V MIXER, MERIDIAN FRONT LOADER 78
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V856000·2018-12-03

    Forest River Recalls 2019 Salem and Wildwood Trailers for Wiring Defect

    Forest River is recalling 2019 Salem and Wildwood recreational trailers because incorrectly wired clearance lights may not work, reducing visibility.

    Product
    FOREST RIVER — FOREST RIVER SALEM, WILDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E111000·2018-12-01

    Luxfer Recalls One-Turn Valves Due to Potential Stem Ejection Risk

    Luxfer Canada Ltd. is recalling One-Turn Valves (part number MPVE-250) because the valve stem may forcibly eject if the knob is turned more than one turn, posing injury and fire risks.

    Product
    FUEL SYSTEM, OTHER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide

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