The Recall Desk

Archive

May 2016 recalls

603 recalls were announced in May 2016.

What the numbers show

Critical
27
Severe
108
High
210
Moderate
211
Low
47

Of the 603 recalls this month scored against our rubric, 4% are Critical, 18% are Severe.

1–100 of 603

  • CriticalNHTSA·16V384000·2016-05-31

    Ford Recalls Vehicles Due to Air Bag Inflator Rupture Risk

    Ford is recalling specific 2005-2011 vehicles because passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.

    Product
    FORD — FORD, MERCURY, LINCOLN MUSTANG, FORD GT, FUSION, MILAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V385000·2016-05-31

    Winnebago Recalls 2015-2016 Motor Homes for Steering Box Defect

    Winnebago is recalling 2015-2016 Tour and Itasca Ellipse motor homes because a steering box defect could cause loss of steering ability.

    Product
    WINNEBAGO — WINNEBAGO, ITASCA TOUR, ELLIPSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V380000·2016-05-31

    Nissan Recalls 2013-2014 Pathfinder Vehicles for Brake Light Switch Defect

    Nissan is recalling 2013-2014 Pathfinder vehicles because an incorrectly installed brake light switch may cause brake lights to stay on or allow shifting out of Park without braking.

    Product
    NISSAN — NISSAN PATHFINDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16182·2016-05-31

    Mirka Recalls Electric Random Orbital Sanders Due to Fire Hazard

    Mirka is recalling approximately 2,500 electric random orbital sanders sold in the U.S. because they can short circuit, posing a fire hazard.

    Product
    Random orbital sanders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V374000·2016-05-27

    Land Rover Recalls Range Rovers Due to Air Bag Inflator Rupture Risk

    Jaguar Land Rover is recalling 2007-2011 Range Rovers in specific US regions because passenger air bag inflators may rupture during deployment, potentially causing serious injury.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V376000·2016-05-27

    Audi Recalls 2008-2009 A4, A5, and Q5 for Air Bag Control Unit Defect

    Volkswagen Group of America is recalling 2008-2009 Audi A4, A5, and Q5 vehicles because the air bag control units may corrode and fail, potentially preventing air bag deployment in a crash.

    Product
    AUDI — AUDI A5, Q5, A4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16E049000·2016-05-27

    Xperion Recalls CNG Fuel Tanks Due to Leak Risk

    Xperion is recalling specific CNG fuel tanks because a neck adapter may pull out, allowing fuel to leak and increasing fire risk.

    Product
    FUEL SYSTEM, OTHER:STORAGE:TANK ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V373000·2016-05-27

    Jaguar Recalls 2009-2011 XF Models for Air Bag Inflator Rupture Risk

    Jaguar is recalling 2009-2011 XF vehicles in specific states because passenger air bag inflators may rupture during a crash, potentially causing serious injury or death.

    Product
    JAGUAR — JAGUAR XF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V375000·2016-05-27

    Coach and Equipment Recalls Buses with Defective Wheelchair Lifts

    Coach and Equipment is recalling 2014-2015 Metro Lite, Pegasus, and Phoenix buses because wheelchair lift platforms may crack or separate, posing an injury risk to operators.

    Product
    COACH AND EQUIPMENT — COACH AND EQUIPMENT PHOENIX, PEGASUS, METRO LITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16179·2016-05-27

    Tommee Tippee Sippee Cups Recalled Due to Mold Risk in Valves

    Mayborn USA is recalling 3.1 million Tommee Tippee Sippee cups because mold can grow in the white valve, posing a risk of gastrointestinal symptoms.

    Product
    Tommee Tippee Sippee spill-proof cups
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • LowUSDA FSIS·045-2016·2016-05-27

    Burger's Ozark Recalls Pulled Pork Due to Incorrect Back Label

    Burger's Ozark Country Cured Hams is recalling approximately 150 pounds of seasoned pulled pork products because the back of the package displays an incorrect label for a beef brisket product.

    Product
    Burger's Ozark Country Cured Hams, Inc. — Recall Notification Report 045-2016 (Pulled Pork Products)
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·16V366000·2016-05-26

    Daimler Trucks Recalls 2015-2016 FCCC Trucks for Steering Defect

    Daimler Trucks North America is recalling 2015-2016 FCCC trucks because a steering box defect could cause sudden loss of steering ability.

    Product
    FCCC — FCCC XBR, XCM, XCR, XBP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V363000·2016-05-26

    Mercedes-Benz Recalls Vehicles Due to Air Bag Inflator Rupture Risk

    Mercedes-Benz is recalling specific 2008-2011 models because passenger air bag inflators may rupture during deployment, potentially causing serious injury or death.

    Product
    MERCEDES BENZ — MERCEDES BENZ, MERCEDES-BENZ C300, C350, C63, GLK350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V367000·2016-05-26

    Toyota Recalls 2015 Yaris Vehicles Due to Front Strut Bearing Defect

    Toyota is recalling 2015 Yaris vehicles because front strut mounting bearings can be damaged by high loads, potentially causing loss of vehicle stability and increasing crash risk.

    Product
    TOYOTA — TOYOTA YARIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16177·2016-05-26

    Rheem Recalls Electric Water Heaters Due to Fire and Burn Hazards

    Rheem is recalling about 54,000 Performance Platinum electric water heaters sold at Home Depot because the control panel can overheat, posing fire and burn risks.

    Product
    Rheem electric water heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V370000·2016-05-26

    Ducati Recalls 2016 XDiavel S Motorcycles Due to Rear Wheel Installation Defect

    Ducati is recalling 925 model year 2016 XDiavel S motorcycles because the rear wheel may be incorrectly installed, which could cause a loss of braking and power transmission, increasing crash risk.

    Product
    DUCATI — DUCATI XDIAVEL S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V362000·2016-05-26

    Kenworth Recalls 2016 W900 Trucks for Headlight Wiring Defect

    PACCAR is recalling 355 model year 2016 Kenworth W900 trucks because they may lose headlights when switching to high beams, increasing crash risk.

    Product
    KENWORTH — KENWORTH W900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V371000·2016-05-26

    Terex Advance Mixer Trucks Recalled for Loose Axle Hex Nuts

    Terex Advance is recalling 2015-2016 Mixer FD3000, FD4000, and FD6000B trucks because improperly tightened axle hex nuts may cause the driveshaft to disconnect, increasing crash risk.

    Product
    TEREX ADVANCE — TEREX ADVANCE MIXER FD3000, MIXER FD6000B, MIXER FD4000
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V369000·2016-05-26

    Startrans Shuttle Buses Recalled for Wheelchair Lift Platform Defects

    Supreme Corporation is recalling 2008-2014 Startrans shuttle buses because wheelchair lift platforms may crack or fall out, posing injury risks.

    Product
    STARTRANS — STARTRANS AZURE HYBRID, PRESIDENT S2, PRESIDENT, CANDIDATE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·044-2016·2016-05-26

    Taylor Farms Recalls Chicken Salads Due to Undeclared Allergens

    Taylor Farms Florida is recalling 151 pounds of Wawa Thai style chicken mango salad because the packaging contains undeclared wheat and sesame allergens.

    Product
    Taylor Farms Florida, Inc. — Taylor Farms Florida Inc. Recalls Salads Containing Chicken Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • HighCPSC·16178·2016-05-26

    Osprey Recalls Child Backpack Carriers Due to Fall Hazard

    Osprey is recalling about 31,000 child backpack carriers because a cut in the plastic buckle can cause the shoulder strap to release, posing a fall hazard to the child.

    Product
    Child backpack carriers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V368000·2016-05-26

    Dejana Recalls Dominator Trucks Due to Potential Crane Cover Detachment

    Dejana is recalling 2013-2016 Dominator trucks because a crane valve bank cover may crack and fall off, creating a road hazard.

    Product
    DEJANA — DEJANA DOMINATOR IV, DOMINATOR-PROPANE, DOMINATOR I, DOMINATOR III
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16176·2016-05-26

    Box Components Recalls BMX Bicycle Forks Due to Fall Hazard

    Box Components is recalling about 4,100 carbon fiber BMX bicycle forks because the steer tube can become loose, posing a fall hazard.

    Product
    Bicycle forks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V365000·2016-05-26

    Trans Tech School Bus Wheelchair Lift Recall for Platform Cracking

    Transportation Collaborative is recalling 2014-2016 Trans Tech school buses equipped with certain Ricon wheelchair lifts due to potential platform cracking or bearing displacement.

    Product
    TRANS TECH BUS — TRANS TECH BUS ST AERO, STUDENT SAFETY TRANSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1614-2016·2016-05-25

    Monteris Medical Recalls NeuroBlate Laser Probes Due to Lens Fracture

    Monteris Medical Corp is recalling 121 NeuroBlate System SideFire Select 2.2 mm Directional Laser Probes because a sapphire lens fractured during a procedure, introducing CO2 into a patient's brain.

    Product
    NeuroBlate System SideFire Select 2.2 mm Directional Laser Probe, Sterile EO. Model #s SFS000-01,SFS002-01, SFS122-01, SFS222-01, SFS322-01, SFS422-01, and SFS522-01. NeuroBlate System SideFire Select Directional Laser Probes are part of the NeuroBlate System. The Monteris Me
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1332-2016·2016-05-25

    Germinados Campo Verde Recalls Alfalfa Sprouts Linked to Salmonella

    Germinados Campo Verde is recalling alfalfa sprouts from Puerto Rico due to a link to seed contaminated with Salmonella.

    Product
    Alfalfa Sprout Product***Germinados Campo Verde***San Sebastian, Puerto Rico
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·16V364000·2016-05-25

    BMW Recalls X5 and X6 Models Due to Air Bag Inflator Rupture Risk

    BMW is recalling specific 2007-2011 X5 and X6 models because the passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.

    Product
    BMW — BMW X5, X6 ACTIVEHYBRID SAC, X6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V361000·2016-05-25

    Subaru Recalls 2003-2004 Models for Air Bag Inflator Rupture Risk

    Subaru is recalling 2003-2004 Legacy, Outback, and Baja vehicles because passenger air bag inflators may rupture during deployment, potentially causing serious injury or death.

    Product
    SUBARU — SUBARU OUTBACK, BAJA, LEGACY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1359-2016·2016-05-25

    Sugarfina Chocolate Malt Balls Recalled for Undeclared Peanuts

    Sugarfina, LLC is recalling Chocolate Malt Balls because they contain undeclared peanuts, a major food allergen.

    Product
    Sugarfina Chocolate Malt Balls UPC Code 840278113565 SKU K1159
    Category
    Food
    Distribution
    25 states
  • SevereFDA (Drugs)·D-0853-2016·2016-05-25

    Keystone Recalls Better Braid Un-Braid Due to Microbial Contamination

    Keystone Laboratories is recalling Better Braid Un-Braid salicylic acid product due to a failed S. aureus test. The product was distributed in Maryland and New Jersey.

    Product
    BETTER BRAIDS UN-BRAID (salicylic acid), Le Demelant, Packaged in 12 FL. OZ. (355 ml) Bottles, Over the Counter Only. Distributed by KEYSTONE LABORATORIES, UPC 07059600430.
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0855-2016·2016-05-25

    Renovo Patch Recalled for Lack of Approval and Subpotency

    TMIG Inc is recalling Renovo Patch because it was marketed without FDA approval and three lots were found to be subpotent.

    Product
    Renovo Patch (Capsaicin, 0.0375%, Menthol, USP 5.00%), 3-count patches per carton, Rx only, Distributed By: TMIG Inc, Marietta , GA 30062, Manufactured By: Pocono Coated Products LLC., Cherryville, NC 28021 NDC: 69176-025-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V359000·2016-05-25

    Subaru and Saab Recall Vehicles for Air Bag Inflator Rupture Risk

    Subaru is recalling specific 2003-2008 vehicles because passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.

    Product
    SUBARU — SUBARU, SAAB OUTBACK, BAJA, LEGACY, IMPREZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V358000·2016-05-25

    Subaru and Saab Recall for Passenger Air Bag Inflator Rupture Risk

    Subaru is recalling specific 2003-2011 models and 2006 Saab 9-2x vehicles because passenger air bag inflators may rupture during deployment, potentially causing serious injury or death.

    Product
    SUBARU — SUBARU, SAAB OUTBACK, BAJA, LEGACY, IMPREZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1372-201·2016-05-25

    Nice! Mixed Fruit Recalled for Potential Glass Contamination

    Milky Way Intl Trading Corp is recalling Nice! Mixed Fruit in 8-ounce jars due to potential glass in the product.

    Product
    Mixed Fruit (In Light Syrup), Net Wt. 8oz (227g), Bottle Label UPC 0-49022-80896-6, Case UPC 100-49022-80896-3
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1680-2016·2016-05-25

    Zimmer Herbert Cannulated Bone Screw Recall for Sterility Concerns

    Zimmer Manufacturing B.V. is recalling specific lots of Herbert Cannulated Bone Screws because a small hole may be present in the inner tray, potentially compromising sterility.

    Product
    Herbert Cannulated Bone Screw System, Bone Screw, 6.5 mm Dia., 45 mm Length 47115504507 Herbert Cannulated Bone Screw System, Bone Screw, 6.5 mm Dia., 75 mm Length 47115507507 Herbert Cannulated Bone Screw System, Bone Screw, 6.5 mm Dia., 90 mm Length 47115509007
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1682-2016·2016-05-25

    Zimmer VersaFx Femoral Fixation System Screws Recalled for Sterility Concerns

    Zimmer Manufacturing B.V. is recalling specific lots of VersaFx Femoral Fixation System screws because a small hole may be present in the inner tray, potentially compromising sterility.

    Product
    VersaFx Femoral Fixation System Hex head compression screw 4.7 mm dia. 2 inch (51 mm) length 47116202400
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1690-2016·2016-05-25

    Becton Dickinson Recalls Shielded IV Catheters Due to Defect

    Becton Dickinson is recalling 1.3 million shielded IV catheters because a defect could cause the catheter to separate or break.

    Product
    1) 24 G x 0.75 in. BD Angiocath" Autoguard" shielded IV catheter (0.7 mm x 19 mm) made of FEP polymer catalog number 381700 2) 24 G x 0.56 in. BD Angiocath-N" Autoguard" shielded IV catheter (0.7 mm x 14 mm) made of FEP polymer catalog number 381720
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V360000·2016-05-25

    Forest River Stealth Evo Recalled for Incorrect Tire Load Range

    Forest River is recalling 2016 Stealth Evo trailers because incorrect tires may fail prematurely, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER STEALTH EVO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16747·2016-05-25

    Hed Cycling Recalls Black Bicycle Rims Due to Crash Hazard

    Hed Cycling is recalling specific black bicycle rims because they can cause brake pads to wear out unexpectedly, posing a crash hazard to riders.

    Product
    Hed Black Rims
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1672-2016·2016-05-25

    Medtronic Recalls Visualase Cooled Laser Applicator Systems Due to Melting Risk

    Medtronic is recalling 120 Visualase Cooled Laser Applicator Systems because the catheters may melt during procedures.

    Product
    Visualase Cooled Laser Applicator System (VCLAS). The VCLAS system consists of the Visualase Laser Diffusing Fiber (LDF) and the Visualase Cooled Catheter System (CCS). The LDF and disposables (including the CCS) is indicated for use to necrotize or coagulate soft tissue th
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1358-2016·2016-05-25

    Bunge Creamy Frying Shortening Recalled for Foreign Material

    Bunge Oil North America Inc. is recalling 1,400 cases of Bunge Creamy Frying Shortening due to the presence of a foreign material inside the jugs.

    Product
    Bunge Creamy Frying Shortening, Partially Hydrogenated Soybean Oil "For All Deep Frying", Net Wt 35 lb (17.4 Liter), Distributed By. IAS International American Supermarkets, 226 Old New Brunswick Road, Piscataway, NJ 08854, Mfd By: Bunge, Bradley, IL 60915, UPC 0 00 78684 69024 4
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-1677-2016·2016-05-25

    Zimmer Manufacturing Recalls Sterile Hip and Trauma Implant Screws

    Zimmer Manufacturing B.V. is recalling specific lots of sterile Hip and Trauma Implant Screws because a small hole may be present in the inner tray.

    Product
    Zimmer Plates and Screws (ZPS) 4.0 mm Cancellous Screw Fully Threaded, 12 mm Length 47484001200 4.0 mm Cancellous Screw Fully Threaded, 14 mm Length 47484001400 4.0 mm Cancellous Screw Fully Threaded, 16 mm Length 47484001600 4.0 mm Cancellous Screw Fully Threaded, 18 mm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1688-2016·2016-05-25

    Alcon Recalls LenSx Lasers Due to Incomplete Corneal Flap Creation

    Alcon is voluntarily recalling 81 LenSx Laser Systems with Corneal Flap Capability due to reports of incomplete corneal flap creation during surgery.

    Product
    LenSx Laser System. Indicated for use in patients undergoing cataract surgery and refractive surgery.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1356-2016·2016-05-25

    Bunge Canola Frying Oil Recalled for Foreign Material Presence

    Bunge Oil North America Inc. is recalling 660 cases of 35 lb Bunge Clear Liquid Canola Frying Oil due to the presence of foreign material inside the jugs.

    Product
    Bunge Clear Liquid Canola Frying Oil (Aceite de Canola para freir liquido y transparente), Net Wt 35 lb (15.88 kg), MFD in USA By: Bunge Oils, St. Louis, MO 63146-1000, UPC 0 00 78684 69266 8
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·F-1375-2016·2016-05-25

    QTrade Organic Ginger Root Tea Recalled for Salmonella Risk

    QTrade Teas & Herbs is recalling Organic Ginger Root Tea Bag Cut due to potential Salmonella contamination. The product was distributed in California, Illinois, New Jersey, and Canada.

    Product
    Organic Ginger Peach Iced Tea, 100x1oz box, item #60001
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1366-2016·2016-05-25

    Empirical Labs Recalls Liposomal Magnesium Supplement for Mold Contamination Risk

    Empirical Labs is recalling Liposomal Magnesium Nutritional Supplement due to potential mold contamination. The recall affects 1,972 bottles sold nationwide.

    Product
    Liposomal Magnesium Nutritional Supplement. 6 FL. OZ (180 ml) The product is packaged in a six ounce, plastic, Royalty Bottle, with a 24mm vented flip top lid. item number: DES004Z. Sold under brands DESBIO and Seeking Health
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1673-2016·2016-05-25

    Zimmer 3.5 mm Cortical Screws Recalled for Potential Sterility Compromise

    Zimmer Manufacturing B.V. is recalling specific lots of 3.5 mm Cortical Screws because a small hole may be present in the inner tray, potentially compromising sterility.

    Product
    Zimmer Plates and Screws (ZPS) 3.5 mm Cortical Screw SelfTapping, 10 mm Length 47483501001 3.5 mm Cortical Screw SelfTapping, 14 mm Length 47483501401 3.5 mm Cortical Screw SelfTapping, 16 mm Length 47483501601 3.5 mm Cortical Screw SelfTapping, 24 mm Length 47483502401
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1678-2016·2016-05-25

    Zimmer Manufacturing Recalls Sterile Hip and Trauma Implant Screws

    Zimmer Manufacturing B.V. is recalling specific lots of sterile Hip and Trauma Implant Screws because a small hole may be present in the inner tray.

    Product
    M/DN Intramedullary Fixation 4.2 mm Diameter Cortical Screw, 3.5 mm Hex Head, 45 mm Length 00225304542 M/DN Intramedullary Fixation 4.2 mm Diameter Cortical Screw, 3.5 mm Hex Head, 70 mm Length 00225307042
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1669-2016·2016-05-25

    Lumenis M22 IPL Acne Filters Recalled for Superficial Burn Risk

    Lumenis Ltd is recalling M22 IPL Acne Filters due to a risk of superficial burns when using the device.

    Product
    Lumenis M22 System Model Number: GA-0005400 (M22 IPL + YAG Module) with Acne Filter (KT-1014971).
    Category
    Medical Device
    Distribution
    12 states
  • HighFDA (Devices)·Z-1671-2016·2016-05-25

    AB Sciex Mass Spectrometers Recalled for Incorrect Quantitative Results

    AB Sciex is recalling two models of mass spectrometers used for in vitro diagnostics because they may report incorrect quantitative results under certain conditions.

    Product
    AB Sciex Triple Quad 4500MD LC/MS/MS System, Part No. 5031257; and QTRAP 4500MD LC/MS/MS System, Part No. 5031231. Mass spectrometers for in vitro diagnostic use only.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-1676-2016·2016-05-25

    Zimmer Manufacturing Recalls Specific Lots of Sterile Hip and Trauma Implant Screws

    Zimmer Manufacturing B.V. is recalling 99 units of sterile Hip and Trauma Implant Screws due to a potential small hole in the inner tray.

    Product
    Periarticular plating system, cancellous bone screw, partially threaded, hex head, 4.0 mm diameter, 16 mm length 47234702116
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1373-2016·2016-05-25

    QTrade Organic Green Tea Hojicha Recalled for Potential Salmonella Contamination

    QTrade Teas & Herbs is recalling Organic Green Tea Hojicha due to the potential for Salmonella contamination. The product was distributed in the US and internationally.

    Product
    Organic Green Tea Hojicha, Net 16 kgs, (bulk product 16 kg boxes with inner liner)
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1371-2016·2016-05-25

    Nice! Peach Slices Recalled for Potential Glass Contamination

    MW Polar Foods is recalling Nice! Peach Slices and Mixed Fruit in 8-ounce jars due to potential glass in the product.

    Product
    Sliced Peaches (In Light Syrup), Net Wt. 8oz (227g), Bottle Label UPC 0-49022-80894-2, Case UPC 100-49022-80894-9
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1341-2016·2016-05-25

    Bunge Canola Frying Oil Recalled for Foreign Material Presence

    Bunge Oil North America Inc. is recalling Taco Bell Liquid Canola Frying Oil due to the presence of a foreign material inside the jugs.

    Product
    Taco Bell Liquid Canola Frying Oil, 35 lb., (15.88 kg), Packaged Exclusively for use by Taco Bell and its franchisees. Taco Bell Corp, Irvine, CA 92618
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-1692-2016·2016-05-25

    Alcon Valved Entry System Recalled for Potential Leakage

    Alcon Research, Ltd. is recalling 83,448 units of 23G and 25G Valved Entry Systems because they may leak beyond design specifications.

    Product
    Alcon 23G and 25G Valved Entry System provides access into the posterior segment of the eye for surgical instruments within the frame of 23G and 25G Pars-Plana-Vitrectomy (PPV) surgeries.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Food)·F-1363-2016·2016-05-25

    UNFI Recalls Commercial Wheat Germ Due to E. coli Contamination

    UNFI is recalling 32 bags of Commercial Wheat Germ 274000 because the product contains generic E. coli. The recall covers distribution in 17 states.

    Product
    COMMERCIAL WHEAT GERM 274000, 50.00 lbs. (22.68 kg); UPC Code: 0-26938-46535-3
    Category
    Food
    Distribution
    16 states
  • HighCPSC·16174·2016-05-25

    TJX Recalls Foldable Lounge Chairs Due to Risk of Injury

    TJX is recalling about 5,200 foldable lounge chairs sold at T.J. Maxx and Marshalls because they can collapse unexpectedly, posing a fall and injury hazard.

    Product
    Foldable lounge chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16746·2016-05-25

    Honda Recalls Mini Tillers Due to Throttle Cable Injury Risk

    Honda is recalling about 219,000 mini tillers because a pinched throttle cable can cause the tines to rotate unexpectedly, posing a risk of serious injury.

    Product
    Mini Tillers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1694-2016·2016-05-25

    Alcon Recalls 23G and 25G Valved Trocar Cannula Custom Paks

    Alcon Research, Ltd. is recalling 30,701 units of 23G and 25G valved trocar cannula Custom Paks because the products have the potential to leak beyond their design specification.

    Product
    Custom Paks containing 23G and 25G valved trocar cannula provide access into the posterior segment of the eye for surgical instruments within the frame of 23G and 25G Pars-Plana-Vitrectomy (PPV) surgeries.
    Category
    Medical Device
    Distribution
    1 state
  • HighNHTSA·16V355000·2016-05-25

    Grand Design RV Recalls 2016-2017 Trailers Due to Propane Leak Risk

    Grand Design RV is recalling 2016-2017 Imagine and Reflection trailers because a propane regulator defect may cause gas leaks and fire.

    Product
    GRAND DESIGN — GRAND DESIGN REFLECTION, IMAGINE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1374-2016·2016-05-25

    QTrade Recalls Organic Ginger Root Tea Due to Salmonella Risk

    QTrade Teas & Herbs is recalling Organic Ginger Root Tea Bag Cut because it has the potential to be contaminated with Salmonella.

    Product
    Organic Ginger Root Tea Bag Cut (TBC), 25 kgs
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1693-2016·2016-05-25

    Alcon Recalls 23G and 25G Constellation Totalplus Paks for Potential Leakage

    Alcon Research, Ltd. is recalling 225,000 units of 23G and 25G Constellation Totalplus Paks because the products have the potential to leak beyond their design specifications.

    Product
    23G and 25G Constellation Totalplus Paks provides access into the posterior segment of the eye for surgical instruments within the frame of 23G and 25G Pars-Plana-Vitrectomy (PPV) surgeries.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Food)·F-1365-2016·2016-05-25

    Michel et Augustin Butter Cookies Recalled for Undeclared Hazelnuts

    Michel et Augustin is recalling Petites baguettes butter cookies due to undeclared hazelnuts caused by miss-packaging.

    Product
    Michel et Augustin brand Petites baguettes butter cookies Dark Chocolate with a pinch of salt, NET WT. 1.58 oz (45g), UPC 81266802016, Product of the Netherlands -- Manufactured for Michel et Augustin SA, 151 rue de Billancourt (Grand Paris) France --- The label states "May cont
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1354-2016·2016-05-25

    Bunge Canola Oil Recalled for Foreign Material Presence

    Bunge Oil North America Inc. is recalling specific lots of Daily Chef Food Service Pure Canola Oil due to the presence of foreign material inside the jugs.

    Product
    Daily Chef Food Service Pure Canola Oil (Aceite de Canola Para Ensaladas), Net/Neto 4.5 Gal (17L) and Net Wt/Peso Neto, 35 lbs. (15.8 kg), Distributed By: Sam's Inc., Bentonville, AR 72716, UPC 0 78742 06149 8
    Category
    Food
    Distribution
    9 states
  • ModerateFDA (Food)·F-1338-2016·2016-05-25

    Bunge Canola Oil Recalled for Foreign Material Presence

    Bunge Oil North America Inc. is recalling Harvest Value Canola Liquid Frying Oil due to the presence of a foreign material inside the jugs.

    Product
    Harvest Value Canola Liquid Frying Oil, 35 lb., (15.88 kg), Distributed By: U.S. Foodservice, Inc,, Rosemont, IL 60018, UPC 5 07 58108 01988 6
    Category
    Food
    Distribution
    9 states
  • ModerateFDA (Food)·F-1362-2016·2016-05-25

    MegaFood Multi for Women 40+ Recalled for Missing Iron Warning

    FoodState, Inc. is recalling MegaFood Multi for Women 40+ multivitamin bottles because the labels lack the required iron warning statement and child-resistant cap.

    Product
    MegaFood Multi for Women 40+, Multivitamin & Mineral Dietary Supplement packaged in glass bottles UPC:5149410321 -Packaged 60 tablets; UPC:5149410322 -Packaged 120 tablets
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1337-2016·2016-05-25

    Bunge Canola Deep Frying Oil Recalled for Foreign Material

    Bunge Oil North America Inc. is recalling specific lots of Nutra-Clear NT Ultra Canola Deep Frying Oil due to the presence of foreign material inside the jugs.

    Product
    Nutra-Clear NT Ultra - Bunge Canola Deep Frying Oil (High Stability), 35 lb., (15.88 kg), MFD in USA by: Bunge Oils, St. Louis, MO 63146-1000, UPC 0 00 78684 72477 2
    Category
    Food
    Distribution
    9 states
  • ModerateFDA (Food)·F-1339-2016·2016-05-25

    Bunge Vegetable Oil Recalled Due to Foreign Material Presence

    Bunge Oil North America Inc. is recalling Harvest Value Clear Vegetable Frying Oil because of foreign material found inside the jugs.

    Product
    Harvest Value Clear Vegetable Frying Oil, 35 lb., (15.88 kg), Distributed By: U.S. Foodservice, Inc,, Rosemont, IL 60018, UPC 5 07 58108 00302 1
    Category
    Food
    Distribution
    9 states
  • ModerateFDA (Food)·F-1349-2016·2016-05-25

    Bunge Canola Frying Oil Blend Recalled for Foreign Material

    Bunge Oil North America Inc. is recalling 1,923 cases of Yum Canola Frying Oil Blend due to the presence of foreign material inside the jugs.

    Product
    Yum Canola Frying Oil Blend, Net Wt., 35 lbs. (15.88 kg), Packaged Exclusively for use by Yum! Brands Global Restaurants, Yum Brands, Louisville, KY 40232
    Category
    Food
    Distribution
    9 states
  • ModerateFDA (Devices)·Z-1681-2016·2016-05-25

    Zimmer Recalls Sterile Hip and Trauma Implant Screws Due to Tray Defect

    Zimmer Manufacturing B.V. is recalling specific lots of sterile hip and trauma implant screws because a small hole may be present in the inner tray.

    Product
    ITST intertrochanteric/subtrochanteric fixation 4.5 mm diameter cortical screw, 3.5 mm hex head, 57 mm length 00225305745
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1686-2016·2016-05-25

    Diamedix IgG Test Kits Recalled Due to Sample Diluent Contamination

    Diamedix Corporation is recalling 588 EBV-VCA and Mumps IgG test kits because a gel-like substance in the sample diluent could compromise performance.

    Product
    Diamedix Is-EBV-VCA IgG Test Kit Diamedix Is-Mumps IgG Test Kit is an EIA procedure intended for the qualitative and semi-quantitative detection of Mumps IgG antibodies as an aid in the diagnosis of Mumps infection.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1336-2016·2016-05-25

    Bunge Soy Clear Fry Oil Recalled for Foreign Material

    Bunge Oil North America Inc. is recalling 3,240 cases of Bunge Soy Clear Fry Oil OU due to the presence of foreign material inside the jugs.

    Product
    Bunge Soy Clear Fry Oil OU, 35 lb., Manufactured by: Bunge Oils, Inc. Kearny, NJ 07032, UPC 00078684692026
    Category
    Food
    Distribution
    9 states
  • ModerateFDA (Food)·F-1335-2016·2016-05-25

    Prayon Recalls Food Grade Phosphoric Acid Due to Cumene Contamination

    Prayon Inc. is recalling specific batches of food grade phosphoric acid due to potential contamination with trace levels of cumene.

    Product
    Phosphoric Acid, 75% and 85% Food Grade (Brand Name PRAYPHOS PPA 75% FG and PRAYPHOS PPA 85% FG)
    Category
    Food
    Distribution
    9 states
  • ModerateFDA (Food)·F-1361-2016·2016-05-25

    Royal Snacks Jalapeno Pistachio Recalled for Undeclared Dyes

    Royal Snacks Inc is recalling Jalapeno Pistachio Royal Size products because they contain undeclared Yellow #5 and Blue #1 dyes.

    Product
    Royal Snacks Jalapeno Pistachio Royal Size
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Food)·F-1342-2016·2016-05-25

    Bunge Vegetable Oil Recalled for Foreign Material Presence

    Bunge Oil North America Inc. is recalling Katy's Kitchen Soybean Salad Oil due to the presence of foreign material inside the jugs.

    Product
    Katy's Kitchen Soybean Salad Oil (Soya Aceite Para Ensalada), Marketed by/Comercializado por Independent Marketing Alliance, Houston, TX 77079, Product of USA/Producto de EE.UU., UPC 0 08 22486 13034 3
    Category
    Food
    Distribution
    9 states
  • ModerateFDA (Devices)·Z-1699-2016·2016-05-25

    FDA Recalls Onset Mixing Pen Due to Missing Use Period Labeling

    Valeant Pharmaceuticals is recalling 7,716 Onset Mixing Pens because the labeling fails to state the 18-month optimal use period from the start of use.

    Product
    Orapharma (Onpharma) Onset Mixing Pen Rx only, Product/Part Number 1054-02. Manufactured for Onpharma Inc. Los Gratos, CA 95030 The Mixing Pen is used to dispense a solution from a standard 3 mL size cartridge into a second fluid container.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1670-2016·2016-05-25

    Siemens ADVIA Chemistry Triglyceride Reagent Recalled for Linearity Defects

    Siemens Healthcare Diagnostics is recalling ADVIA Chemistry Triglyceride reagent lots 348297 and 359932 because they fail linearity claims near end of shelf life.

    Product
    ADVIA Chemistry Triglyceride_2, concentrated; TRIG_c; Catalog # SMN # 10697575. For in vitro diagnostic use in the quantitative measurement of triglycerides in human serum and plasma on ADVIA Chemistry systems.
    Category
    Medical Device
    Distribution
    16 states
  • ModerateFDA (Devices)·Z-1683-2016·2016-05-25

    Zimmer Manufacturing Recalls Hip and Trauma Implant Screws Due to Tray Defect

    Zimmer Manufacturing B.V. is recalling specific lots of sterile Hip and Trauma Implant Screws because a small hole may be present in the inner tray.

    Product
    Hgp ii acetabular cup bone screw selftap 6.5x15mm 00662406515 Hgp ii acetabular cup bone screw selftap 6.5x20mm 00662406520 Hgp ii acetabular cup bone screw selftap 6.5x25mm 00662406525 Hgp ii acetabular cup bone screw selftap 6.5x35mm 00662406535 Hgp ii acetabular cup bone s
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1685-2016·2016-05-25

    Diamedix Is-Mumps IgG Test Kit Recalled Due to Sample Diluent Contamination

    Diamedix Corporation is recalling 697 Is-Mumps IgG Test Kits because a gel-like substance was found in the sample diluent, which could compromise product performance.

    Product
    Diamedix Is-Mumps IgG Test Kit Diamedix Is-Mumps IgG Test Kit is an EIA procedure intended for the qualitative and semi-quantitative detection of Mumps IgG antibodies as an aid in the diagnosis of Mumps infection.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1344-2016·2016-05-25

    Bunge Recalls Old World Canola Oil Due to Foreign Material

    Bunge Oil North America Inc. is recalling 35-pound jugs of Old World Canola Oil because of the presence of a foreign material inside the containers.

    Product
    Old World Canola Oil (Aceite de Canola), Net Wt. 35 lbs. (15.88 kg), MFD in USA By: Bunge Oils, St. Louis, MO 63146-1000, UPC 0 00 78684 70020 2
    Category
    Food
    Distribution
    9 states
  • ModerateFDA (Devices)·Z-1668-2016·2016-05-25

    Anspach Otologic Diamond Ball Burrs Recalled for Missing Coating

    The Anspach Effort, Inc. is recalling 27 Otologic Curved Micro Diamond Ball Burrs because they may be missing the diamond coating or be the incorrect size.

    Product
    ANSPACH, Rx only, Otologic Curved Micro (OCCM) Diamond Ball Burr, 2.0 MM, Part # OCM7-2SD Product Usage: The Otologic Curved Micro (OCCM) Attachment and burrs are intended for cutting and shaping bone primarily in otology procedures such as cochleostomies.
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1667-2016·2016-05-25

    Anspach Otologic Diamond Ball Burrs Recalled for Missing Coating

    The Anspach Effort, Inc. is recalling specific lots of Otologic Curved Micro Diamond Ball Burrs because they may lack the diamond coating or be the incorrect size.

    Product
    ANSPACH, Rx only, Otologic Curved Micro (OCCM) Diamond Ball Burr, 1.5 MM, Part # OCM7-15SD Product Usage: The Otologic Curved Micro (OCCM) Attachment and burrs are intended for cutting and shaping bone primarily in otology procedures such as cochleostomies.
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1687-2016·2016-05-25

    Diamedix IgG Test Kits Recalled Due to Gel-Like Substance in Diluent

    Diamedix Corporation is recalling 94 Is-EBV-EA-D and Is-Mumps IgG Test Kits because a gel-like substance was found in the sample diluent, potentially compromising performance.

    Product
    Diamedix Is-EBV-EA-D IgG Test Kit Diamedix Is-Mumps IgG Test Kit is an EIA procedure intended for the qualitative and semi-quantitative detection of Mumps IgG antibodies as an aid in the diagnosis of Mumps infection.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1347-2016·2016-05-25

    Bunge Creamy Soy Liquid Frying Oil Recalled for Foreign Material

    Bunge Oil North America Inc. is recalling 2,040 cases of Bunge Creamy Soy Liquid Frying Oil due to the presence of foreign material inside the jugs.

    Product
    Bunge Creamy Soy Liquid Frying Oil (Aceite de Soja Para Freir Liquido y Cremosa), Net Wt. 35 lbs. (15.88 kg), MFD in USA By: Bunge Oils, St. Louis, MO 63146-1000, UPC 0 00 78684 73353 8
    Category
    Food
    Distribution
    9 states
  • ModerateFDA (Food)·F-1364-2016·2016-05-25

    Buell's Orchard Recalls Trader Joe's Apple Cider Due to Patulin

    Buell's Orchard is recalling Trader Joe's Apple Cider because patulin was detected at 63.7 ppb. The product was distributed in Massachusetts and Pennsylvania.

    Product
    TRADER JOE'S Apple Cider, NOT FROM CONCENTRATE SHAKE WELL NO PRESERVATIVES 100% JUICE PASTEURIZED. PERISHABLE, KEEP REFRIGERATED. NET 64 FL OZ (2 QT) 1.89 L. UPC: 0016 4580.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-1346-2016·2016-05-25

    Bunge Soybean Oil Recalled Due to Foreign Material in Jugs

    Bunge Oil North America Inc. is recalling specific lots of Old World Soybean Oil because of the presence of a foreign material inside the jugs.

    Product
    Old World Soybean Oil (Aceite de Soja), Net Wt.35 lbs. (15.88 kg), MFD in USA By: Bunge Oils, St. Louis, MO 63146-1000, UPC 0 00 78684 70011 0
    Category
    Food
    Distribution
    9 states
  • ModerateFDA (Food)·F-1343-2016·2016-05-25

    Bunge Smart Source Soybean Oil Recalled for Foreign Material

    Bunge Oil North America Inc. is recalling 1,080 cases of Smart Source Clear Soybean Frying Oil due to the presence of a foreign material inside the jugs.

    Product
    Smart Source Clear Soybean Frying Oil (Aceite de Soya Transparente Para Freir), Net Wt./Peso Neto 35 lbs. (15.88 kg), Marketed by/Comercializado por Independent Marketing Alliance, Houston, TX 77079, UPC 0 08 22486 13046 6
    Category
    Food
    Distribution
    9 states
  • ModerateFDA (Food)·F-1348-2016·2016-05-25

    Bunge Smart Source Creamy Soybean Frying Oil Recalled for Foreign Material

    Bunge Oil North America Inc. is recalling 60 cases of Smart Source Creamy Soybean Frying Oil due to the presence of foreign material inside the jugs.

    Product
    Smart Source Creamy Soybean Frying Oil (Aceite de Soja Cremosa Para Freir), Net Wt./Peso Neto, 35 lbs. (15.88 kg), Marketed by/Comercializado por Independent Marketing Alliance, Houston, TX 77079, Product of USA/Producto de EE.UU., UPC 0 08 22486 13045 9
    Category
    Food
    Distribution
    9 states
  • ModerateFDA (Food)·F-1350-2016·2016-05-25

    Bunge Vegetable Oil Recalled Due to Foreign Material Presence

    Bunge Oil North America Inc. is recalling specific lots of vegetable oil because foreign material was found inside the jugs.

    Product
    Nathan's Pure Corn Oil, Net Weight 35 lb (15.88 kg), Packed Exclusively for: Nathan's, General Offices: One Jericho Plaza, Jericho, NY 11753, UPC 0 07 16071 99955 5
    Category
    Food
    Distribution
    9 states
  • ModerateFDA (Food)·F-1353-2016·2016-05-25

    Bunge Daily Chef Soybean Oil Recalled for Foreign Material

    Bunge Oil North America Inc. is recalling Daily Chef Food Service Pure Soybean Oil due to the presence of foreign material inside the jugs.

    Product
    Daily Chef Food Service Pure Soybean Oil (Aceite de Soya), Net/Neto 4.5 Gal (17L) and Net Wt/Peso Neto, 35 lbs. (15.8 kg), Distributed By: Sam's West Inc., Bentonville, AR 72716, UPC 0 78742 06151 1
    Category
    Food
    Distribution
    9 states

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