The Recall Desk

Archive

October 2015 recalls

479 recalls were announced in October 2015.

What the numbers show

Critical
22
Severe
124
High
217
Moderate
88
Low
28

Of the 479 recalls this month scored against our rubric, 5% are Critical, 26% are Severe.

401–479 of 479

  • SevereNHTSA·15V634000·2015-10-08

    Volvo Recalls VNL Trucks Due to APU Mounting Defect

    Volvo is recalling 2012-2014 VNL trucks because Electric Auxiliary Power Units may detach, creating a road hazard and increasing crash risk.

    Product
    VOLVO — VOLVO VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V632000·2015-10-08

    KME Predator Emergency Vehicles Recalled for Front Suspension Defect

    KME is recalling 2013-2015 Predator emergency vehicles because loose front ball joints may separate, causing loss of steering control and increasing crash risk.

    Product
    KME — KME PREDATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V631000·2015-10-08

    Navistar Recalls 2016 International Trucks Due to Engine Stalling Risk

    Navistar is recalling specific 2016 International trucks because the engine control module may short circuit, causing the engine to stall without warning and increasing crash risk.

    Product
    INTERNATIONAL — INTERNATIONAL DURASTAR, LONESTAR, PAYSTAR, PROSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16006·2015-10-08

    Safety 1st Recalls Décor Wood Highchairs Due to Fall Hazard

    Safety 1st is recalling about 35,000 Décor Wood highchairs because children can remove the tray, posing a fall hazard. The company has received 68 reports of tray removal, including 11 injuries.

    Product
    Décor Wood Highchair
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1830-2015·2015-10-07

    Hartley Medical Recalls Non-Sterile Prolotherapy with Phenol Vials

    Hartley Medical Center Pharmacy is recalling 10 vials of Prolotherapy with Phenol due to non-sterility concerns. The product was distributed in California and Nevada.

    Product
    Prolotherapy with Phenol (Dextrose 25%, Glycerin 25%, Phenol 2.5%, QS SWI), 100 mL vial, Rx Only, Hartley Medical, (888) 671-2888
    Category
    Drug
    Distribution
    2 states
  • CriticalFDA (Food)·F-3254-2015·2015-10-07

    Real Foods Harvest Slaw Kit Recalled for Undeclared Peanuts

    Real Foods, LLC is recalling Harvest Slaw Kits because peanuts were inadvertently added to the product instead of sunflower seeds, and the labels do not declare peanuts.

    Product
    Harvest Slaw Kit, product ID 028-07114, package in bulk case, Net wt. 5.75 lbs. (2.61 kg). UPC 0 45009 07114 9. The product is labeled in parts "***T/H HARVEST SLAW KIT***Ingredients: Brussels Sprouts, Turnips, Carrots, Sunflower Seeds (sunflower kernels, roasted in vegetable
    Category
    Food
    Distribution
    2 states
  • CriticalCPSC·16005·2015-10-07

    Bed Handles Inc. Recalls Portable Bed Handles Due to Entrapment Deaths

    Bed Handles Inc. is recalling approximately 113,000 portable bed handles sold without safety retention straps. The recall follows reports of four deaths caused by entrapment in gaps between the handle and mattress.

    Product
    Portable bed handles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-3251-2015·2015-10-07

    Ice Cream Club Recalls Caramel Caribou Ice Cream for Undeclared Peanuts

    The Ice Cream Club, Inc. is recalling Caramel Caribou Ice Cream because it contains undeclared peanuts, a major food allergen.

    Product
    Caramel Caribou Ice Cream, 3 gal, frozen in bulk round container.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3256-2015·2015-10-07

    Hill Country Fare Spring Water Recalled for Possible Undeclared Milk Allergen

    Hill Country Fare Natural Spring Water is being recalled due to a possible undeclared milk allergen. The product was distributed in Texas.

    Product
    Hill Country Fare Natural Spring Water 1 GAL./3.78L container packaged in polyethylene jug
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2743-2015·2015-10-07

    MicroPort Recalls Profemur Plus Modular Neck Hip Prosthesis Components

    MicroPort Orthopedics is recalling Profemur Plus modular neck hip prosthesis components due to an unexpected rate of postoperative fractures requiring revision surgery.

    Product
    PROFEMUR PLUS CoCr MODULAR NECK, REF: PHAC1254, SIZE LONG, ORIENTATION 8 degree VAR/VAL. 12/14 SLT Taper. Orthopedic hip prosthesis component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V629000·2015-10-07

    Hyundai Recalls 2011 Elantra and Sonata for Front Coil Spring Fracture Risk

    Hyundai is recalling 28,157 model year 2011 Elantra and Sonata vehicles because road salt may corrode front coil springs, potentially causing them to fracture and puncture tires.

    Product
    HYUNDAI — HYUNDAI ELANTRA, SONATA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1829-2015·2015-10-07

    Hartley Medical Recalls Prolotherapy with Phenol Vials Due to Non-Sterility

    Hartley Medical Center Pharmacy is recalling 14 vials of Prolotherapy with Phenol due to non-sterility concerns. The product was distributed in California and Nevada.

    Product
    Prolotherapy with Phenol (Dextrose 25%, Glycerin 10%, Lidocaine HCl 10%, Bupivacaine HCl 0.625%, Phenol 1%, QS SWI), 5 mL vial, Rx Only, Hartley Medical, (888) 671-2888
    Category
    Drug
    Distribution
    2 states
  • SevereNHTSA·15V628000·2015-10-07

    BMW Recalls 2014-2016 MINI and i3 Vehicles for Air Bag Defect

    BMW is recalling specific 2014-2016 MINI and i3 vehicles because the passenger air bag may not deploy properly in a low-speed crash, increasing injury risk.

    Product
    MINI — MINI, BMW COOPER, I3, COOPER S, JOHN COOPER WORKS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1833-2015·2015-10-07

    Medistat RX Recalls Sterile Products Due to Sterility Assurance Concerns

    Medistat RX L.L.C. is recalling all sterile products, including various injectable medications, due to a lack of assurance of sterility.

    Product
    All Products Intended to be Sterile, mediStat Pharmacy, 110 East Azalea Ave., Foley, AL 36535, 844*737*2550. An Incomplete List of Recalled Products Includes 1) All Cyanacobalamin Products, 2) All Magnesium Chloride Products, 3) All Lipostat (MIC B12) Products, 4) All Trimix (Pa
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2825-2015·2015-10-07

    Arrow Kits with Medtronic Syringes Recalled for Compromised Sterility

    Arrow International Inc. is recalling Arrow Kits containing Medtronic Covidien 0.9% Sodium Chloride Flush Syringes due to compromised sterility of the outer barrel.

    Product
    Arrow Kits with Medtronic Covidien 0.9% Sodium Chloride Flush Syringes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V627000·2015-10-07

    Volkswagen Recalls 2015 Jetta, Golf, and E-Golf for Air Bag Defect

    Volkswagen is recalling 993 model year 2015 Jetta, Golf, and E-Golf vehicles because the passenger air bag may not deploy properly in a crash.

    Product
    VOLKSWAGEN — VOLKSWAGEN JETTA, E-GOLF, GOLF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0002-2016·2015-10-07

    Biosense Webster Recalls Carto 3 EP Navigation System Due to Image Loss

    Biosense Webster is recalling the Carto 3 EP Navigation System because the ultrasound image may disappear during use, requiring a system restart.

    Product
    Carto 3 EP Navigation System. Electro physiology system which views of the electrical activity of the heart through real-time data on 3-D, color-coded cardiac maps.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V630000·2015-10-07

    Volvo Recalls 2015-2016 Trucks for Headlight Intensity Defect

    Volvo is recalling 2015-2016 VAH and VHD trucks because some headlights do not meet federal intensity requirements, increasing crash risk.

    Product
    VOLVO — VOLVO VAH, VHD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2822-2015·2015-10-07

    MicroAire LipoTower Recalled for Potential Electrical Shock Hazard

    MicroAire Surgical Instruments is recalling 168 LipoTower units due to a risk of electrical shock if internal lead wires detach and the ground connection fails.

    Product
    ASP-1021 LipoTower with Aspiration Pump and Tumescent Pump. Medical use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3249-2015·2015-10-07

    ConAgra Recalls CiCi's Cavatappi Macaroni Due to Undeclared Egg

    ConAgra Foods is recalling CiCi's Cavatappi macaroni because egg-containing product was mixed with non-egg product, creating an undeclared allergen.

    Product
    CiCi's Cavatappi, Enriched Macaroni Product, packaged in 5-lb. bags, 4 bags per case, Packed exclusively for use by CiCi's Pizza and its Franchisees, JMC Restaurant Distribution, LP, Coppell, TX.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2823-2015·2015-10-07

    Medtronic Solera Screwdrivers Recalled for Tip Deformation Risk

    Medtronic Navigation is recalling 2,346 Solera screwdrivers used in spine surgery because specific conditions may cause the tips to deform or break.

    Product
    P/N: 9735023, DRIVER 9735023 SOLERA 5.5/6.0 MAS; P/N: 9735024, DRIVER 9735024 SOLERA 5.5/6.0 MAS CAN; P/N: 9735025, DRIVER 9735025 SOLERA 5.5/6.0 RMAS; P/N: 9735026, DRIVER 9735026 SOLERA 5.5/6.0 RMAS CAN; P/N: 9735027,DRIVER 9735027 SOLERA 5.5/6.0 FAS/SAS. The Medtronic Navig
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0003-2016·2015-10-07

    Biosense Webster Recalls SOUNDSTAR eco Diagnostic Ultrasound Catheters

    Biosense Webster is recalling SOUNDSTAR eco 8F and 10F Diagnostic Ultrasound Catheters because the ultrasound image may disappear if the CARTO 3 system restarts during a pericardial effusion.

    Product
    SOUNDSTAR eco 8F and 10F Diagnostic Ultrasound Catheters. For intra-cardiac and intra-luminal visualization of cardiac and great vessel anatomy and physiology as well as visualization of other devices in the heart.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1832-2015·2015-10-07

    Eagle Pharmacy Recalls Subpotent Lipo B Sterile Injection Vials

    Eagle Pharmacy is recalling 104 vials of Lipo B Sterile Injection due to trace amounts of methylcobalamin. The product was distributed in Alabama and Tennessee.

    Product
    LIPO B STERILE INJECTION 10 mL ( Methionine 25 mg, Inositol 50 mg, Choline Chloride 50 mg, Pyridoxine Hydrochloride 5 mg, Methylcobalamin 0.1mg, Benzyl Alcohol, Sterile Water, Sodium Hydroxide, Hydrochloric Acid), Multidose vial, Rx Only, Compounded by Eagle Pharmacy, Birmingha
    Category
    Drug
    Distribution
    2 states
  • HighFDA (Devices)·Z-2821-2015·2015-10-07

    MicroAire LipoTower Recall Due to Electrical Shock Risk

    MicroAire Surgical Instruments is recalling three LipoTower units with aspiration pumps due to a potential risk of electrical shock if internal lead wires detach.

    Product
    ASP-1020 LipoTower with Aspiration Pump. Medical use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·16701·2015-10-07

    BRP Recalls Youth Can-Am ATVs Due to Fuel Filter Fire Hazard

    BRP is recalling about 240 Youth Model Can-Am DS 90 and DS 90X ATVs because a fuel filter defect can cause leaks and fire. No injuries have been reported.

    Product
    Youth Model Can-Am all-terrain vehicles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3247-2015·2015-10-07

    Russet House Recalls Frozen Sweet Potato Fries Due to Undeclared Gluten

    Russet House is recalling specific lots of America's Choice frozen sweet potato fries because they contain undeclared gluten. The product was distributed in six northeastern states.

    Product
    America's Choice Straight Cut Sweet Potatoes Fries, Frozen 539 g in plastic bag. Distributed by: ONPOINT Inc. Montvale, NJ. Product of Canada UPC: 7 54807 12025 5
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0001-2016·2015-10-07

    US Endoscopy Recalls Histolock Resection Device Due to Sterility Concerns

    US Endoscopy Group Inc is recalling 41 units of the Histolock Resection Device because the company cannot assure the sterility of the affected lot.

    Product
    Histolock Resection Device, US Endoscopy. An electrosurgical device designed to be used to endoscopically grasp, dissect and transect tissue during gastrointestinal endoscopic procedures.
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Food)·F-3255-2015·2015-10-07

    Real Foods Broccoli Salad Kit Recalled for Undeclared Peanuts

    Real Foods, LLC is recalling 13 cases of Broccoli Salad Kit because peanuts were inadvertently added instead of sunflower seeds, and the label does not declare peanuts.

    Product
    Broccoli Salad Kit, product ID; 028-07092, packaged in a bulk case, Net wt. 11 lbs (4.99 kg). UPC: 0 45009 07092 0 The product is labeled in parts "***BROCCOLI SALAD KIT***Ingredients: Ingredients: Broccoli, Broccoli Slaw (broccoli, carrots, red cabbage), Coleslaw Dressing (hi
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-3248-2015·2015-10-07

    General Mills Recalls Cascadian Farm Organic Cut Green Beans for Listeria

    General Mills is recalling specific lots of Cascadian Farm Organic Cut Green Beans because one package tested positive for Listeria monocytogenes.

    Product
    Cascadian Farm Organic Cut Green Beans, Net Wt. 10 oz (284g) Keep Frozen.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3257-2015·2015-10-07

    KAL Amino Acid Complex Recalled for Undeclared Milk Allergen

    Nutraceutical International is recalling KAL Amino Acid Complex because the ingredient list does not explicitly state 'milk,' despite containing casein.

    Product
    KAL Brand Amino Acid Complex UPC 021245 51610 1, Product #51610
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2824-2015·2015-10-07

    Medtronic Navigated Solera Screwdrivers Recalled for Potential Tip Deformation

    Medtronic Navigation is recalling 2,346 Navigated Solera Screwdrivers used in spine surgery because specific use conditions may cause the tips to deform or break.

    Product
    P/N: 9734856, SCREWDRIVER, 9734856, SOLERA STD MAST; P/N: 9734857, SCREWDRIVER, 9734857, SOLERA RDN MAST; P/N: 9734279, SCREWDRIVER 9734279 SOLERA STANDARD; and P/N: 9734373, SCREWDRIVER 9734373 SOLERA REDUCTION. The Medtronic Navigated Solera Screwdrivers are reusable devices
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2826-2015·2015-10-07

    Ferno iNX Wheeled Stretcher Recalled for Telescoping Load Frame Defect

    Ferno-Washington Inc is recalling 72 Ferno iNX Wheeled Stretchers because hole elongation in the load frame may allow the retention pin to move.

    Product
    Ferno iNX Wheeled Stretcher, Integrated Patient Transport & Loading System Product Usage: Stretcher for pre-hospital patient transport.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2820-2015·2015-10-07

    Zimmer Recalls Guide Wires Due to Incorrect Expiration Date Labeling

    Zimmer, Inc. is recalling 112,568 sterile guide wires because the labels state a 10-year expiration date, while testing supports only 5 years.

    Product
    Zimmer Guide Wires for orthopedic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0005-2016·2015-10-07

    Guthy-Renker Recalls Subpotent Rodan & Fields Proactiv Foundation

    Guthy-Renker LLC is recalling Rodan & Fields Proactiv Solution compact foundation because the salicylic acid ingredient is subpotent.

    Product
    Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic acid acne treatment, DARK, 7 g/0.25 OZ. Compacts, Over the Counter. Manufactured for Guthy-Renker Palm Desert, CA 92250.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-3250-2015·2015-10-07

    Sun Kee Mixed Fruit Candy Recalled for Undeclared Dyes

    Prosperity Resources is recalling Sun Kee Mixed Fruit Candy because it contains undeclared colors and an unallowable dye.

    Product
    Mixed Fruit Candy, Net Wt. 12 oz. (340g), Distributed by: Prosperity Resources Int'l, Inc., Product of China, UPC 6 47406 02091 3
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2819-2015·2015-10-07

    Sterilmed Recalls Reprocessed Zimmer Tourniquet Cuffs Due to Mislabeling

    Sterilmed is recalling 43 reprocessed Zimmer tourniquet cuffs because they are labeled as single hose but are actually dual hose devices.

    Product
    Zimmer, Reprocessed Zimmer Tourniquet Cuffs,34" Single Hose Single Bladder Brown (PLC), 34", Model (Reprocessor) Number: ZIM60-7075-106, Reprocessed by Sterilmed. Products are individually packaged in a Tyvek¿/poly pouch. There are 5 pouches placed inside a casepack box. Each
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0004-2016·2015-10-07

    Lifeline Systems Recalls Philips GoSafe Mobile Help Button Due to Battery Issues

    Lifeline Systems is recalling 8,616 Philips GoSafe Mobile Help Button devices because irregular battery disconnection can cause charging issues.

    Product
    Philips GoSafe Mobile Help Button; 7000MHB. Personal Emergency Response System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-3258-2015·2015-10-07

    Coquette's Gluten Free Cupcakes Recalled for Incorrect Allergen Labeling

    Coquette's Bistro and Bakery is recalling 120 packages of gluten-free cupcakes because the label incorrectly states the product contains no egg or dairy, despite containing both.

    Product
    Coquette's Gluten Free Spring Pack Cupcakes (4 pack), Oranges n' Cream & Strawberry Mint Lemonade. coquettesbistro.com. NET Wt. 9.67 OZ. No expiration date on package, sold in ambient air at retail.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-0001-2016·2015-10-07

    Guthy-Renker Recalls Rodan & Fields Proactiv Foundation for Subpotent Salicylic Acid

    Guthy-Renker LLC is recalling Rodan & Fields Proactiv Solution Compact Foundation because the salicylic acid ingredient is subpotent.

    Product
    Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic acid acne treatment, FAIR, 7 g/0.25 OZ. Compacts, Over the Counter. Manufactured for Guthy-Renker Palm Desert, CA 92250.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2818-2015·2015-10-07

    Olympus Recalls Gastrovideoscope Due to Insufficient Cleaning Accessory Information

    Olympus is recalling 1,014 EVIS EXERA II Gastrovideoscopes because specific cleaning accessories required for reprocessing were not provided.

    Product
    EVIS EXERA II Gastrovideoscope OLYMPUS GF type UCT180; designed for endoscopic real-time ultrasound imaging, ultrasound guided needle aspiration and other endoscopic procedures within the upper gastrointestinal tract and surrounding organs.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1831-2015·2015-10-07

    VistaPharm Recalls Metoclopramide Oral Solution Due to Defective Container Lids

    VistaPharm is recalling 84,100 cups of Metoclopramide Oral Solution because the unit dose cup lids are not fully qualified.

    Product
    METOCLOPRAMIDE ORAL SOLUTION, USP 10 mg/10 mL, 10 mL cups, Rx only. Manufactured by VistaPharm, Inc, Largo, FL. NDC: 66689-031-01.
    Category
    Drug
    Distribution
    6 states
  • LowFDA (Drugs)·D-0002-2016·2015-10-07

    Rodan & Fields Proactiv Foundation Recalled for Subpotent Salicylic Acid

    Guthy-Renker LLC is recalling Rodan & Fields Proactiv Solution compact foundation because the salicylic acid ingredient is subpotent.

    Product
    Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic acid acne treatment, LIGHT, 7 g/0.25 OZ. Compacts, Over the Counter. Manufactured for Guthy-Renker Palm Desert, CA 92250.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0003-2016·2015-10-07

    Guthy-Renker Recalls Subpotent Rodan & Fields Proactiv Foundation

    Guthy-Renker LLC is recalling Rodan & Fields Proactiv Solution Compact Foundation because the salicylic acid ingredient is subpotent.

    Product
    Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic acid acne treatment, MEDIUM, 7 g/0.25 OZ. Compacts, Over the Counter. Manufactured for Guthy-Renker Palm Desert, CA 92250.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-3259-2015·2015-10-07

    Imperial Sugar Recalls Granulated Sugar Due to Foreign Matter

    Savannah-Imperial LP is recalling 50-pound bags of Imperial Sugar granulated sugar because blue fiber was detected in the product.

    Product
    Imperial Sugar, Pure Granulated Sugar, Net wt. 50 lbs (22.6 kg), Distributed by Imperial-Savannah LP, Sugar Land, Texas 77478.
    Category
    Food
    Distribution
    17 states
  • LowFDA (Food)·F-3260-2015·2015-10-07

    West Creek Granulated Sugar Recalled for Foreign Matter

    Savannah-Imperial LP is recalling West Creek Extra Fine Granulated Sugar because blue fiber was detected in the product.

    Product
    West Creek, Extra Fine Granulated Sugar, Net Wt. 25 lbs (11.3 kg), Distributed by Performance Food Group, Richmond, VA 23238.
    Category
    Food
    Distribution
    17 states
  • LowFDA (Food)·F-3265-2015·2015-10-07

    Imperial Sugar Recalls 2000 lb Bags Due to Foreign Matter

    Savannah-Imperial LP is recalling 2000 lb bags of Imperial GMI Non GMO Linerless Sugar EFG because blue fiber was detected in the product.

    Product
    Imperial GMI, Non GMO Linerless Sugar EFG, Net Weight 2000 lbs., Imperial Sugar Company, Savannah, GA.
    Category
    Food
    Distribution
    17 states
  • LowFDA (Food)·F-3264-2015·2015-10-07

    Dixie Crystals Sugar Recalled for Foreign Matter Detection

    Savannah-Imperial LP is recalling specific lots of Dixie Crystals sugar due to the detection of blue fiber in the product.

    Product
    Dixie Crystals, Sugar EFG, Net Weight 50 lbs and 2000 lbs., Imperial Sugar Company, Savannah, GA.
    Category
    Food
    Distribution
    17 states
  • LowFDA (Drugs)·D1834-2015·2015-10-07

    Apotex Recalls Verapamil Hydrochloride Extended-Release Tablets for Dissolution Failure

    Apotex Inc. is recalling 2,075 bottles of Verapamil Hydrochloride Extended-Release tablets, 240 mg, because one lot failed to meet dissolution specification limits.

    Product
    Verapamil Hydrochloride Extended-Release tablets, USP, 240 mg, 500-count bottles, Rx Only, Apotex Corp. Manufactured by Apotex Research Private Limited, Bangalore, Karnataka 560 099, India; Manufactured for: Apotex Corp., Weston, FL 33326. NDC 60505-2742-5.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-3262-2015·2015-10-07

    Savannah-Imperial Recalls Clear Value Sugar Due to Foreign Matter

    Savannah-Imperial LP is recalling Clear Value Sugar because blue fiber was detected in the product.

    Product
    Clear Value Sugar, granulated, Net Wt. 4 lbs (1.81 kg), Distributed by Topco Associates LLC, 7711 Gross Point Road, Skokie, IL 60077.
    Category
    Food
    Distribution
    17 states
  • LowFDA (Food)·F-3263-2015·2015-10-07

    Kroger Granulated Sugar Recalled for Foreign Matter Detection

    Savannah-Imperial LP is recalling PSST Granulated Sugar distributed by Kroger due to the detection of blue fiber in the product.

    Product
    PSST, Granulated Sugar, Net Wt. 4 lbs (1.81 kg), Distributed by Kroger Co., Cincinnati, OH 45202.
    Category
    Food
    Distribution
    17 states
  • LowFDA (Food)·F-3266-2015·2015-10-07

    Laura Lynn Pure Cane Sugar Recalled for Foreign Matter

    Savannah-Imperial LP is recalling Laura Lynn Pure Cane Sugar because blue fiber was detected in the product.

    Product
    Laura Lynn, Pure Cane Sugar, Net Wt. 25 lbs (11.34 kg), Distributed by Ingles Markets, Inc., Asheville, NC 26816.
    Category
    Food
    Distribution
    17 states
  • LowFDA (Food)·F-3261-2015·2015-10-07

    Monarch Granulated Sugar Recalled for Foreign Matter Detection

    Savannah-Imperial LP is recalling Monarch Granulated Sugar due to the detection of blue fiber in the product.

    Product
    Monarch, Granulated Sugar, Net Wt. 25 lbs and 50 lbs (22.88 kg), Distributed by US Foods, Inc., Rosemont, IL.
    Category
    Food
    Distribution
    17 states
  • LowFDA (Drugs)·D-0004-2016·2015-10-07

    Guthy-Renker Recalls Subpotent Rodan & Fields Proactiv Foundation

    Guthy-Renker LLC is recalling specific lots of Rodan & Fields Proactiv Solution Compact Foundation because the salicylic acid ingredient is subpotent.

    Product
    Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic acid acne treatment, TAN, 7 g/0.25 OZ. Compacts, Over the Counter. Manufactured for Guthy-Renker Palm Desert, CA 92250.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E082000·2015-10-06

    Dorman Aftermarket Steering Shafts Recalled for Potential Separation Risk

    Dorman is recalling aftermarket steering shafts for 1995-2002 Ford, Mercury, and Lincoln vehicles because they may separate, causing loss of steering control.

    Product
    MERCURY — MERCURY, FORD, LINCOLN GRAND MARQUIS, CROWN VICTORIA, TOWN CAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V625000·2015-10-06

    Winnebago and Itasca Motorhomes Recalled for Liquid Propane Hose Fire Risk

    Winnebago is recalling 2013-2016 Era, Trend, Tour, Journey, and Itasca motorhomes because a liquid propane hose may harden and leak, increasing fire risk.

    Product
    ITASCA — ITASCA, WINNEBAGO MERIDIAN, JOURNEY, TOUR, NAVION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V626000·2015-10-06

    Kia Recalls 2011-2013 Sorento for Brake-Shift Interlock Defect

    Kia is recalling 2011-2013 Sorento vehicles because the brake-shift interlock may fail, allowing the car to roll out of Park without the brake being pressed.

    Product
    KIA — KIA SORENTO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15E083000·2015-10-06

    Meritor Recalls Axles Due to Loose Caliper Bolts

    Meritor is recalling specific axle assemblies because caliper bolts may not be properly tightened. This defect could cause the caliper to detach, reducing braking performance and increasing crash risk.

    Product
    SERVICE BRAKES, AIR:DISC:CALIPER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E080000·2015-10-05

    SAF-Holland Recalls Trailer Axles Due to Spindle Separation Risk

    SAF-Holland is recalling specific 5-inch tapered trailer axles because the wheel end may separate from the axle, increasing the risk of a crash.

    Product
    SUSPENSION:REAR:AXLE:SPINDLE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V623000·2015-10-05

    Daimler Recalls 2016 Thomas Built Buses Due to Engine Stalling Risk

    Daimler Trucks North America is recalling 2016 Thomas Built Bus Saf-T-Liner C2 school buses because the engine control module may short circuit, causing the engine to stall without warning.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15E081000·2015-10-05

    Hale K Gearboxes Recalled for Shifting Out of Gear in Fire Apparatus

    Hale Products Inc. is recalling K Gearboxes used in fire apparatus that may shift from road to neutral while in transit, potentially increasing crash risk.

    Product
    POWER TRAIN:MANUAL TRANSMISSION recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V620000·2015-10-02

    Daimler Trucks Recalls 2016 Freightliner and Western Star Vehicles for Engine Stalling

    Daimler Trucks is recalling 2016 Freightliner, Western Star, and Thomas Built Buses vehicles because a faulty engine control module may cause the engine to stall without warning, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, THOMAS BUILT BUSES, WESTERN STAR 122SD, MT55, BUSINESS CLASS M2, 114SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V621000·2015-10-02

    Mazda Recalls 2015-2016 Mazda3 Vehicles for Fuel Tank Valve Defect

    Mazda is recalling 2015-2016 Mazda3 vehicles because a fuel tank shut-off valve defect may cause fuel leaks or engine stalls, increasing fire and crash risks.

    Product
    MAZDA — MAZDA MAZDA3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V622000·2015-10-02

    Snake River Recalls 2015-2016 Horse Trailers Due to Axle Weld Failure

    Snake River Trailer Company is recalling 2015-2016 Horse trailers because a weld on the rear axle may fail, causing the wheel assembly to separate and increasing crash risk.

    Product
    SNAKE RIVER — SNAKE RIVER HORSE TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V619000·2015-10-02

    C&B Quality Trailer Works Recalls 2015-2016 Horse Trailers Due to Axle Weld Failure

    C&B Quality Trailer Works is recalling 79 model year 2015-2016 horse trailers because a weld on the torsion arm assembly may fail, allowing the wheel to separate from the trailer.

    Product
    C&B QUALITY TRAILER WORKS — C&B QUALITY TRAILER WORKS HORSE TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·101-2015 expansion·2015-10-02

    Aspen Foods Recalls Frozen Raw Stuffed Chicken Products Due to Salmonella Risk

    Aspen Foods is recalling approximately 561,000 pounds of frozen, raw, stuffed, and breaded chicken products due to possible Salmonella Enteritidis contamination.

    Product
    Aspen Foods Recalls Frozen, Raw, Stuffed & Breaded Chicken Products Due to Possible Salmonella Enteritidis Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·16003·2015-10-01

    BSH Recalls Bosch, Gaggenau, Kenmore Elite, and Thermador Dishwashers for Fire Hazard

    BSH Home Appliances is recalling approximately 149,000 dishwashers because the power cords can overheat, posing a fire hazard. Consumers should stop using the units and contact the company for a free repair.

    Product
    Bosch, Gaggenau, Kenmore Elite and Thermador Dishwashers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V617000·2015-10-01

    Daimler Trucks Recalls 2015-2016 Freightliner and Western Star Trucks

    Daimler Trucks is recalling 2015-2016 Freightliner and Western Star trucks because the transmission may lock or cause the vehicle to move backward unexpectedly.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR 114SD, BUSINESS CLASS M2, 108SD, CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V618000·2015-10-01

    Ford Recalls 2016 Fusion and Lincoln MKZ for Fuel Tank Defect

    Ford is recalling 2016 Fusion and Lincoln MKZ vehicles because fuel tanks may have insufficient wall thickness, posing a fire risk if cracked in a crash.

    Product
    LINCOLN — LINCOLN, FORD MKZ, FUSION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V616000·2015-10-01

    Freightliner Trucks Recalled for Fifth Wheel Locking Mechanism Failure

    Daimler Trucks North America is recalling 2011-2014 Freightliner trucks because the fifth wheel locking mechanism may fail, risking trailer detachment.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA, BUSINESS CLASS M2, COLUMBIA GLIDER, CORONADO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16001·2015-10-01

    Pier 1 Imports Recalls Katerina Outdoor Patio Swivel Armchairs

    Pier 1 Imports is recalling Katerina outdoor patio swivel armchairs because they can tip backward while rocking, posing a fall hazard.

    Product
    Katerina Swivel Armchairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide

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