The Recall Desk

Archive

October 2012 recalls

969 recalls were announced in October 2012.

What the numbers show

Critical
242
Severe
210
High
389
Moderate
113
Low
15

Of the 969 recalls this month scored against our rubric, 25% are Critical, 22% are Severe.

501–600 of 969

  • HighFDA (Food)·F-0258-2013·2012-10-24

    Spartan Central Kitchen Recalls Creamy Redskin Potato Salad Due to Listeria

    Spartan Central Kitchen is voluntarily recalling 5-pound Creamy Redskin Potato Salad manufactured between August 20 and September 10, 2012, due to possible Listeria contamination.

    Product
    #301 Creamy Redskin Potato Salad 5 pounds
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0225-2013·2012-10-24

    Spartan Central Kitchen Recalls Spinach Dip Due to Listeria Contamination

    Spartan Central Kitchen is voluntarily recalling 5-pound cans of Spinach Dip manufactured between August 20 and September 10, 2012, due to possible Listeria contamination found during an FDA inspection.

    Product
    #341 Spinach Dip 5 pounds
    Category
    Food
    Distribution
    2 states
  • HighNHTSA·12V517000·2012-10-24

    Altec Recalls 2011-2012 CFD 1217 Wood Chippers Due to Blade Defect

    Altec is recalling 2011-2012 CFD 1217 wood chippers because blades may not meet hardness specifications, posing a risk of injury if they fail.

    Product
    ALTEC — ALTEC CFD 1217 WOOD CHIPPER
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0109-2013·2012-10-24

    Earth's Best Organic Wheat Teething Biscuits Recalled for Metal Fragments

    Lovin Oven, LLC is recalling Earth's Best Organic Wheat Teething Biscuits because they may contain very small metal fragments.

    Product
    Earth's Best Organic Wheat Teething Biscuits, 6 pack, UPC # 23923-90015, HCG#C90615
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0067-2013·2012-10-24

    ConMed Linvatec Recalls PressFT Sutures Due to Driver Tip Separation Risk

    ConMed Linvatec is recalling PressFT HI-FI Sutures because the driver tip may separate from the shaft after implant insertion.

    Product
    "***PressFT***2.1 w/ One #2 (5 metric) Hi-Fi***Suture***NP211***2009-02***CONMED LINVATEC 11311 CONCEPT BLVD LARGO, FL 33773-4908 USA*** To reattach soft tissue to bone in orthopedic surgical procedures
    Category
    Medical Device
    Distribution
    17 states
  • HighFDA (Food)·F-0234-2013·2012-10-24

    Spartan Central Kitchen Recalls Italian Rotini Salad Due to Listeria

    Spartan Central Kitchen is voluntarily recalling 5-pound Italian Rotini Salad manufactured in August and September 2012 due to possible Listeria contamination found during an FDA inspection.

    Product
    #331 Italian Rotini Salad 5 pounds
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0191-2013·2012-10-24

    Spartan Central Kitchen Recalls Shepherd's Pie Due to Listeria Contamination

    Spartan Central Kitchen is voluntarily recalling 10 oz Shepherd's Pie products manufactured in August and September 2012 due to possible Listeria contamination found during an FDA inspection.

    Product
    #427 10 oz Shepherd's Pie 10 ounces
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0250-2013·2012-10-24

    Spartan Central Kitchen Recalls Wild Rice Salad Due to Listeria Risk

    Spartan Central Kitchen is voluntarily recalling #311 Fruit & Nut Wild Rice Salad due to possible Listeria contamination found during an FDA inspection.

    Product
    #311 Fruit & Nut Wild Rice Salad 311 5 pounds
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0160-2013·2012-10-24

    Spartan Central Kitchen Recalls Garden Fresh Salads for Listeria Risk

    Spartan Central Kitchen is voluntarily recalling Garden Fresh salads due to possible Listeria contamination found during an FDA inspection.

    Product
    #762 Salad - Large Garden Fresh 3/4 pounds #761 Salad - Small Garden Fresh 3 oz.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0241-2013·2012-10-24

    Spartan Central Kitchen Recalls Chicken Salad Base Due to Listeria

    Spartan Central Kitchen is voluntarily recalling 5-pound Chicken Salad Base products manufactured between August 20 and September 10, 2012, due to possible Listeria contamination found during an FDA inspection.

    Product
    #322 Chicken Salad Base 5 pounds
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0092-2013·2012-10-24

    Osteotech Recalls Grafton and Xpanse Bone Graft Products Due to Sterility Concerns

    Osteotech Inc is recalling multiple lots of Grafton and Xpanse bone graft products because the sterility of the inner pouch surface may be compromised.

    Product
    Grafton DBM Orthoblend Large Defect Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone matrix (DBM) allograft. It is intended for use as a bone graft extender, bone gr
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0058-2013·2012-10-24

    Belmont Rapid Infuser Recalled Due to Electrical Flash Hazard

    Belmont Instrument Corporation is recalling 2,913 Rapid Infuser units because saline leakage caused an electrical flash at the power entry area.

    Product
    Belmont Rapid Infuser, a Fluid Management System, Model FMS2000.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0113-2013·2012-10-24

    Sunshine Peanut Company Recalls Peanut Butter Due to Aflatoxin Levels

    Sunshine Peanut Company is recalling Sunny Boy and Sunshine Peanut Brand peanut butter because routine USDA sampling found aflatoxin levels exceeding 20 ppb.

    Product
    Sunny Boy Peanut Butter. Product is labeled in part: 6/5 lb tubs- "SunnyBoy Creamy PEANUT BUTTER***Net Wt. 5lb. (2.27KG)***INGREDIENTS: Peanuts, Dextrose, Contains less than 2% of the following: Salt, Partially Hydrogenated Oil (Rapeseed Cottonseed And/Or Mono-Diglycerides)**
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-0086-2013·2012-10-24

    Osteotech Recalls Grafton and Xpanse Bone Graft Products Due to Sterility Concerns

    Osteotech Inc is recalling multiple lots of Grafton and Xpanse bone graft products because the sterility of the inner pouch surface may be compromised.

    Product
    Grafton DBM A-Flex Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone matrix (DBM) allograft. It is intended for use as a bone graft extender, bone graft substitute and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0209-2013·2012-10-24

    Spartan Central Kitchen Recalls Taco Layer Dip Due to Listeria Risk

    Spartan Central Kitchen is voluntarily recalling specific Taco Layer Dip products in Michigan and Ohio due to possible Listeria contamination found during an FDA inspection.

    Product
    #371 Taco Layer Dip - 30 oz., #370 Taco Layer Dip, 15 oz.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0090-2013·2012-10-24

    Osteotech Recalls Grafton and Xpanse Bone Graft Products Due to Sterility Concerns

    Osteotech is recalling multiple lots of Grafton and Xpanse bone graft products because the sterility of the inner pouch surface may be compromised.

    Product
    Grafton DBM Orthoblend Small Defect Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone matrix (DBM) allograft. It is intended for use as a bone graft extender, bone gra
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0224-2013·2012-10-24

    Spartan Central Kitchen Recalls Vegetable Dip Due to Listeria Contamination

    Spartan Central Kitchen is voluntarily recalling 5-pound Vegetable Dip products manufactured in August and September 2012 due to possible Listeria contamination found during an FDA inspection.

    Product
    #342 Vegetable Dip 5 pounds
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0259-2013·2012-10-24

    Spartan Central Kitchen Recalls Watermelon Products Due to Listeria Contamination

    Spartan Central Kitchen is voluntarily recalling bulk and tray watermelon products manufactured between August 20 and September 10, 2012, due to possible Listeria contamination found during an FDA inspection.

    Product
    #234 Bulk Watermelon 234 2.5 pounds and #050 Watermelon Tray 16 ounces
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0280-2013·2012-10-24

    Spartan Central Kitchen Recalls Salad Topper Due to Listeria Contamination

    Spartan Central Kitchen is voluntarily recalling 8-ounce Salad Topper products manufactured in August and September 2012 due to possible Listeria contamination found during an FDA inspection.

    Product
    #022 Salad Topper 8 ounces
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0210-2013·2012-10-24

    Spartan Central Kitchen Recalls Cheddar Free Ham & Onion Cheeseballs

    Spartan Central Kitchen is recalling 12-ounce Cheddar Free Ham & Onion Cheeseballs in Michigan and Ohio due to possible Listeria contamination.

    Product
    #363 Cheddar Free Ham & Onion Cheeseball 12 ounces
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0288-2013·2012-10-24

    Spartan Central Kitchen Recalls Egg Salad Sandwiches Due to Listeria Risk

    Spartan Central Kitchen is voluntarily recalling #747 Egg Salad Sandwiches on White manufactured in August and September 2012 due to possible Listeria contamination found during an FDA inspection.

    Product
    #747 Egg Salad Sandwich on White
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0151-2013·2012-10-24

    Spartan Central Kitchen Recalls Pound Cake Due to Listeria Contamination

    Spartan Central Kitchen is voluntarily recalling 12-ounce pound cakes manufactured between August 20 and September 10, 2012, due to possible Listeria contamination found during an FDA inspection.

    Product
    Pound Cake 12 ounces
    Category
    Food
    Distribution
    2 states
  • HighCPSC·13018·2012-10-24

    Rivers Edge Recalls Hunter Tree Stands Due to Fall Hazard

    Rivers Edge is recalling about 14,000 hunter tree stands because snap-hook assemblies can fail, causing the stand and user to fall.

    Product
    Tree Stands for Hunters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0123-2013·2012-10-24

    Southwind Foods Recalls Frozen Snapper Fill IQF for Mislabeling

    Southwind Foods is recalling 145 cases of frozen snapper fill IQF because the product was mislabeled and misleading.

    Product
    Frozen Red Cod Fillet (Red Snapper) Individually Quick Frozen was labeled and identified as Snapper FILL IQF (ROCKFISH). 1/10 lb, code #14343.
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0082-2013·2012-10-24

    Aesculap Recalls Two Columbus Femoral Cutting Guides Due to Marking Error

    Aesculap, Inc. is recalling two Columbus 4-IN-1 Femoral Cutting Guide Instruments because the laser markings for size identification are incorrect, although the instruments are correctly dimensioned.

    Product
    Columbus 4-IN-1 Femoral Cutting Guide M3 Instrument (NQ083R)
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Food)·F-0294-2013·2012-10-24

    Sun Boricua Pa'l Mundo Recalls Crabmeat-Filled Turnovers for Undeclared Color Additives

    Sun Boricua Pa'l Mundo Inc. is recalling crabmeat-filled turnovers in Puerto Rico because they contain undeclared color additives.

    Product
    "Tacos de Jueyes" (Crabmeat-filled turnovers)***Keep Refrigerated***Manufacturado por Sun Boricua Pa'l Mundo Inc, Carr. 486 km 0.1 Bo. Quebrada, Camuy PR 00627
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0076-2013·2012-10-24

    Anspach Effort Recalls Electric Foot Controls Due to Cable Shield Defect

    The Anspach Effort, Inc. is recalling 10 electric foot controls used for bone cutting because the cable lacks a shield connection.

    Product
    "***Electric Systems Foot Control with Direction and Irrigation***Rx Only***" Product Usage: Cutting and shaping bone including bones of the spine and cranium.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0071-2013·2012-10-24

    Terumo Backplate Replacement CXFVR 1500 Holder Recalled for Incorrect Configuration

    Terumo is recalling 33 Backplate Replacement CXFVR 1500 Holders because they were manufactured with an incorrect configuration of connector supports.

    Product
    Terumo Backplate Replacement CXFVR 1500 Holder The Flexible venous Reservoir is mounted on the Backplate/Holder and secures the flexible reservoir by strategically placed mounting arms. Additionally, there are three port supports the user incorporates to position the lines tha
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0296-2013·2012-10-24

    Sun Boricua Pa'l Mundo Shrimp Turnovers Recalled for Undeclared Color Additives

    Sun Boricua Pa'l Mundo Inc. is recalling shrimp-filled turnovers in Puerto Rico because they contain undeclared color additives.

    Product
    "Tacos de Camarones" (Shrimp-filled turnovers)***Keep Refrigerated***Manufacturado por Sun Boricua Pa'l Mundo Inc, Carr. 486 km 0.1 Bo. Quebrada, Camuy PR 00627
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0059-2013·2012-10-24

    Beckman Coulter Recalls Unicel Closed Tube Aliquotter Units Due to Hardware Error

    Beckman Coulter is recalling 18 Unicel Closed Tube Aliquotter units because a hardware motion error may occur. The recall covers units distributed in the US and several international locations.

    Product
    Unicel Closed Tube Aliquotter (UCTA) for UniCel DxC 660i, UniCel DxC 680i, UniCel DxC 860i, UniCel DxC 880i Synchron Access Clinical Systems. Part Number A45853. Product Usage: The UniCel DxC Synchron Clinical Systems are fully automated, computer-controlled clinical chemist
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0293-2013·2012-10-24

    Sun Boricua Lobster-Filled Turnovers Recalled for Undeclared Color Additives

    Sun Boricua Pa'l Mundo Inc. is recalling lobster-filled turnovers in Puerto Rico due to undeclared color additives.

    Product
    "Tacos de Langosta" (Lobster-filled turnovers)***Keep Refrigerated***Manufacturado por Sun Boricua Pa'l Mundo Inc, Carr. 486 km 0.1 Bo. Quebrada, Camuy PR 00627
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0080-2013·2012-10-24

    Boston Scientific Recalls Leveen Needle Electrodes Due to Incorrect Portuguese Instructions

    Boston Scientific is recalling Leveen Coaccess Needle Electrodes because the Portuguese instructions for use contain errors. The recall affects units distributed in Brazil, Portugal, and Hong Kong.

    Product
    Leveen Coaccess Needle Electrode (3.5/15) and (4.0/15). Disposable, monopolar, electrosurgical devices, intended for use in conjunction with BSC radiofrequency generator for the thermal coagulation necrosis of soft tissues, including partial or complete ablation of nonresect
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Food)·F-0295-2013·2012-10-24

    Sun Boricua Pa'l Mundo Recalls Marlin-Filled Turnovers for Undeclared Color Additives

    Sun Boricua Pa'l Mundo Inc. is recalling 36,000 units of Marlin-filled turnovers in Puerto Rico due to undeclared color additives.

    Product
    "Tacos de Marlin" (Marlin-filled turnovers)***Keep Refrigerated***Manufacturado por Sun Boricua Pa'l Mundo Inc, Carr. 486 km 0.1 Bo. Quebrada, Camuy PR 00627
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0075-2013·2012-10-24

    Anspach Effort Recalls Electric Systems Foot Control Due to Cable Defect

    The Anspach Effort, Inc. is recalling 41 Electric Systems Foot Controls because the foot control cable lacks a shield connection.

    Product
    "***Electric Systems Foot Control with Direction Only***Rx Only***" Product Usage: Cutting and shaping bone including bones of the spine and cranium.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-009-2013·2012-10-24

    Earthborn Products Recalls Colloidal Silver Supplement for Lack of FDA Approval

    Earthborn Products is recalling 161 gallons of colloidal silver supplements because the FDA determined the product is misbranded and not generally recognized as safe and effective.

    Product
    Colloidal Silver, 100 ppm TDS, Natural Mineral Supplement, sold in a) 2 fl.oz (59.15 mL), b) 8 fl.oz (236.6 mL), c) 16 fl.oz (473.2 mL), d) 32 fl.oz (946.4 mL), e) 64 fl.oz (1.89 L), and f) 1 Gal. (3.78 L), Distributed by: Earthborn Products, San Diego, CA 92103.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0121-2013·2012-10-24

    Pepsi Beverages Recalls Mislabeled Diet Crush Orange Soda Cans

    Pepsi Beverages Company is recalling 1,791 cases of Diet Crush Orange Soda in Arizona due to mislabeling involving new graphics on the previous formulation.

    Product
    Diet Crush Orange Soda, 12 oz cans
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0062-2013·2012-10-24

    Zimmer Recalls CPT Hip Stems Due to Incorrect Packaging Cartons

    Zimmer Inc. is removing CPT hip stems from the market because they were packaged in incorrect cartons and distributed domestically and internationally.

    Product
    CPT Femoral Stem 12/14 Neck Taper Extended Offset,(item 00-8114-001-10. CPT stems are primary cemented femoral hip stems used by surgeons in total hip arthroplasty.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0081-2013·2012-10-24

    Boston Scientific Recalls Leveen Coaccess Introducer Sets for Incorrect Portuguese Instructions

    Boston Scientific is recalling 19,716 Leveen Coaccess Introducer Sets because the Portuguese instructions for use contain errors. The devices were distributed in Brazil, Portugal, and Hong Kong.

    Product
    Leveen Coaccess Introducer Set. Disposable, monopolar, electrosurgical devices, intended for use in conjunction with BSC radiofrequency generator for the thermal coagulation necrosis of soft tissues, including partial or complete ablation of nonresectable liver lesions.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0061-2013·2012-10-24

    Zimmer Recalls CPT Hip Stems Due to Incorrect Packaging

    Zimmer, Inc. is removing CPT Hip System femoral stems from the market because they were packaged in incorrect cartons and distributed internationally and domestically.

    Product
    CPT Hip System Femoral Stem Petite, Item No. 00-8011-000-05. CPT stems are primary cemented femoral hip stems used by surgeons in total hip arthroplasty.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0297-2013·2012-10-24

    SunFresh Natural Pitted Prunes Recalled for Unapproved Color and Undeclared Ingredient

    SunFresh Natural LLC is recalling 1,200 bags of 6-ounce pitted prunes nationwide because the product contains unapproved Rhodamine B45170 and undeclared sorbic acid.

    Product
    SunFresh Natural Pitted Prunes Net wt. 6 oz. Distributed by: Sunfresh Natural LLC, Passaic, NJ 07055 Please visit us at: www.sunfreshnatural.com
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0060-2013·2012-10-24

    Zimmer Recalls CPT Modular Hip Stems Due to Packaging Errors

    Zimmer Inc. is removing CPT Modular Hip Stems from the market because they were packaged in incorrect cartons and distributed internationally and domestically.

    Product
    CPT Modular Stem, Item No. 00-8011-001-00; Lot 61947708. CPT stems are primary cemented femoral hip stems used by surgeons in total hip arthroplasty.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0079-2013·2012-10-24

    Boston Scientific Recalls LeVeen Needle Electrode Systems for Incorrect Portuguese Instructions

    Boston Scientific is recalling LeVeen Standard Needle Electrode Systems because the Portuguese instructions for use are incorrect. The recall affects units distributed in Brazil, Portugal, and Hong Kong.

    Product
    LeVeen Standard Needle Electrode System, Sterile (3.5/12), (3.5/15), (4.0/15), (3.5/25), (5.0/15), (5.0/25), and (4.0/25). Disposable, monopolar, electrosurgical devices, intended for use in conjunction with BSC radiofrequency generator for the thermal coagulation necrosis of
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Devices)·Z-0073-2013·2012-10-24

    Sunquest Laboratory Software Recall for Calculation Errors in Online Entry

    Sunquest Information Systems is recalling Sunquest Laboratory software versions 6.4.0 and later due to potential calculation errors in the Online Entry application.

    Product
    Sunquest Laboratory : intended for use by professionals working in a clinical laboratory.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·13017·2012-10-23

    Dorel Recalls Eddie Bauer Rocking Wood Bassinets Due to Suffocation Hazard

    Dorel Juvenile Group is recalling approximately 97,000 Eddie Bauer Rocking Wood Bassinets because a locking mechanism failure can cause the bassinet to tip, posing a suffocation risk to infants.

    Product
    Eddie Bauer Rocking Wood Bassinets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V512000·2012-10-23

    Express Cargo Trailers Recalled for Potential Wheel Separation Risk

    Express Trailers is recalling 2011-2012 Cargo trailers because aluminum wheels may not be tightened to proper torque, potentially leading to wheel separation.

    Product
    EXPRESS — EXPRESS CARGO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·13016·2012-10-23

    JELD-WEN Recalls Interior Bifold Doors Due to Pivot Pin Impact Hazard

    JELD-WEN is recalling about 170,800 interior bifold doors because the lower pivot pin can break, causing the door to fall and pose an impact hazard.

    Product
    JELD-WEN and Reliabilt Interior Bifold Doors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·13015·2012-10-23

    Summit Treestands Recalls Crush Series Perch, Stoop, and Ledge Units

    Summit Treestands is recalling about 2,900 Crush Series Perch, Stoop, and Ledge tree stands because the hanging strap assembly could fail, posing a fall hazard.

    Product
    Summit Treestands Crush Series Perch, Stoop and Ledge treestands for hunters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·13012·2012-10-23

    ValcoBaby Joey Booster Seats Recalled Due to Fall Hazard

    ValcoBaby is recalling about 975 Joey booster toddler seats because the attachment mechanism can disengage, allowing a child to fall from the stroller.

    Product
    ValcoBaby "Joey" booster toddler seats for strollers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·12E047000·2012-10-22

    Timken Recalls Front Wheel Hubs for Jeep Liberty Vehicles

    Timken is recalling front wheel hubs that may be mistakenly installed on 4x2 Jeep Liberty vehicles, posing a risk of wheel separation and crash.

    Product
    JEEP — JEEP LIBERTY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V516000·2012-10-22

    Thor Motor Coach Recalls Four Winds Motorhomes Due to Fire Risk

    Thor Motor Coach is recalling 634 Four Winds motorhomes from model years 2008-2010 because a defective transfer switch may overheat and cause a fire.

    Product
    FOUR WINDS — FOUR WINDS PRESIDIO, CHATEAU, DUTCHMEN, FUN MOVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·12V513000·2012-10-19

    Eldorado Buses Recalled for Defective Emergency Window Handles

    Eldorado National is recalling 2011 Axess and E-Z Rider II Max buses because emergency egress window handles may break, potentially trapping passengers.

    Product
    ELDORADO — ELDORADO AXESS, E-Z RIDER II MAX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V505000·2012-10-18

    Van Hool Recalls 2012 TD925 Motorcoaches Due to Fuel Leak Fire Risk

    Van Hool is recalling 136 model year 2012 TD925 motorcoaches because a tire blowout could damage the fuel filter, causing a leak and potential fire.

    Product
    VAN HOOL — VAN HOOL TD925
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V519000·2012-10-18

    Mack Trucks Recalls 2008-2009 Models Due to Retarder Control Box Fire Risk

    Mack Trucks is recalling 260 model year 2008-2009 GU, LEU, and MRU trucks because a control box may lose its electrical ground, potentially causing localized overheating and a vehicle fire.

    Product
    MACK — MACK MRU, GU, LEU
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V509000·2012-10-18

    Navistar Recalls 2012 International Trucks Due to Passenger Seat Defect

    Navistar is recalling 2012 International DuraStar and Workstar trucks because the front passenger seat may separate from its mounting rails, increasing injury risk in a crash.

    Product
    INTERNATIONAL — INTERNATIONAL DURASTAR, WORKSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V511000·2012-10-18

    Prevost Recalls 2012-2013 Coach Buses Due to Fire Risk

    Prevost is recalling 2012-2013 X3-45 and XLII-45 buses because power cables may rub against sharp edges, causing a short-circuit and potential vehicle fire.

    Product
    PREVOST — PREVOST XLII-45 ENTERTAINER, X3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·13014·2012-10-18

    Dream On Me Recalls Happy Swing II Infant Swings Due to Strangulation Hazard

    Dream On Me is recalling Happy Swing II infant swings because the opening between the tray or grab bar and the seat can allow a child's body to pass through, posing a strangulation hazard.

    Product
    Happy Swing II infant swings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·13013·2012-10-18

    Dream On Me Recalls Bistro High Chairs Due to Strangulation Hazard

    Dream On Me is recalling Bistro high chairs because openings in the seat and tray can allow a child's neck to become entrapped, posing a strangulation risk.

    Product
    Bistro high chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0034-2013·2012-10-17

    Cut Fruit Express Recalls Fruit Trays Due to Salmonella Risk

    Cut Fruit Express is recalling specific fruit trays with dip because the cantaloupe used was found to test positive for Salmonella.

    Product
    CANTALOUPE, HONEYDEW, PINEAPPLE AND RED GRAPE, DIP: H.Brooks 33478 FRUIT TRAY w/dip 2.5# Net Wt 40 oz (1134 g) 292 2 per case UPC# 0 3823233478 5. H.Brooks 38279 FRUIT TRAY w/Dip 3# Net Wt 48 oz (1361g) 2 per case 101 UPC# 03823238279 3. H.Brooks 38287 FRUIT TRAY w/Di
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0100-2013·2012-10-17

    Manna Organics Recalls Soybean Sprouts Due to Listeria Risk

    Manna Organics is recalling 16-ounce packages of SooNyeoWon Healthy Soybean Sprouts because they may be contaminated with Listeria monocytogenes.

    Product
    SooNyeoWon Healthy Soybean Sprouts, 16 ounce package; Manna Organics Inc. 170 Avenue 'L', Newark, NJ 07105; MSB West, LLC 622 South Anderson Street, Los Angeles, CA 90023
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0048-2013·2012-10-17

    3fish Recalls HT Premium Lobster Cake Due to Listeria-Contaminated Onions

    3fish Inc. is recalling HT Premium Lobster Cake because it was made with diced onions contaminated with Listeria monocytogenes.

    Product
    HT Premium Lobster Cake (fresh), 3 oz @ 2x8ct, Net Wt: 3 lbs, Packed by 3fish, Inc.
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-0028-2013·2012-10-17

    FDA Recalls Organic Pine Nuts Due to Potential Peanut Contamination

    Newark Nut Stores is recalling 870 lbs of organic pine nuts nationwide because they may contain peanuts.

    Product
    Organic Pine Nuts (Raw, No Shell) 1 lb.Nuts.com NutsOnline, 125 Moen Street, Cranford, NJ 07016 800-558-8881
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0029-2013·2012-10-17

    Cut Fruit Express Recalls Mixed Fruit Due to Salmonella

    Cut Fruit Express is recalling mixed fruit products containing cantaloupe, honeydew, pineapple, and grapes due to a positive Salmonella sample.

    Product
    CANTALOUPE, HONEY DEW, PINEAPPLE AND GRAPES (CHPG) UNDER THE FOLLOWING BRANDS: Indianhead Foods 13105 FRUIT MIX CHPG 5# Manufactured by Cut Fruit Express Mpls, MN 55076 Following products Distributed by H. Brooks & Co. Mpls, MN 55112: H.Brooks & Company 31165 MIXED F
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0089-2013·2012-10-17

    G.O. Fresh Recalls Fruit Mix With Orange Wedges Due to Salmonella Risk

    G.O. Fresh is voluntarily recalling specific fruit mix products containing cantaloupe due to potential Salmonella contamination linked to a supplier recall.

    Product
    SYSCO Imperial 47340104/5# FRUIT MIX W/ORANGE WEDGES 130250 BEST BY 9/16/12, UPC# 0007 4865498029.
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-0080-2013·2012-10-17

    Spokane Produce Recalls Pico De Gallo Due to Salmonella Risk

    Spokane Produce, Inc. is recalling 16 oz containers of Pineapple/Mango Pico De Gallo because the mangoes used in the product may be contaminated with Salmonella.

    Product
    Pico De Gallo in a plastic container labeled: "Pineapple/Mango Pico De Gallo Roma Tomato, Pineapple, Mango, Red Onion, Green Bell Pepper, Anaheim Pepper, Cilantro Lime Juice, jalapeno Pepper, Salt 88694 83987 Keep Refrigerated Best used by: 09/10/12 Packed by Spokane Produce,
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Devices)·Z-0019-2013·2012-10-17

    Accutron Recalls Flowmeter Packages for Incorrect Gas Function

    Accutron is recalling 220 Flowmeter packages used in analgesia gas machines because they may function incorrectly when nitrous gas flows without oxygen.

    Product
    CM Flowmeter Pkg H, Model #36700, Serial # 13749 Product Usage: Conscious Sedation Unit Analgesia Gas Machine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0099-2013·2012-10-17

    Manna Organics Soy Milk Recalled for Potential Listeria Contamination

    Manna Organics Inc. is recalling 220 units of 1.3-gallon soy milk due to potential Listeria monocytogenes contamination. The product was distributed across ten states.

    Product
    Soy Milk, 1.3 gallon, packaged in a white plastic pail, UPC 0 28346 07140 9. Produced by Manna Organics Inc. 170 Avenue 'L', Newark, NJ 07105.
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0084-2013·2012-10-17

    Eco Health Recalls florAlign Prebiotic Formula Due to Salmonella Risk

    Eco Health is recalling florAlign Prebiotic Formula in 90g, 180g, and 270g sizes because it may be contaminated with Salmonella.

    Product
    florAlign Prebiotic Formula, sizes: 90g, 180g, 270g
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0042-2013·2012-10-17

    3fish Inc. Recalls Frozen Carolina Style Crab Cakes Due to Listeria

    3fish Inc. is recalling frozen Carolina Style Crab Cakes because they contain diced onions previously recalled for Listeria monocytogenes contamination.

    Product
    Carolina Style Crab Cakes (Frozen), 2 x 8ct  INGLES, Net Wt 4 lbs, Packed by 3fish, Inc.
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-0049-2013·2012-10-17

    3fish Recalls Jalapeno Salmon Cakes Due to Listeria-Contaminated Onions

    3fish Inc. is recalling Jalapeno Salmon Cakes because they were made with diced onions previously recalled for Listeria monocytogenes contamination.

    Product
    Jalapeno Salmon Cake 3oz (Fresh), 4 oz @ 2x8ct, Net Wt: 3 lbs, Packed by 3fish, Inc.
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-0044-2013·2012-10-17

    3fish Recalls Frozen Crab Cakes Due to Listeria-Contaminated Onions

    3fish Inc. is recalling frozen MD Crab Cakes because they were manufactured with diced onions contaminated with Listeria monocytogenes.

    Product
    MD Crab Cakes - Value Tray Pack (Frozen), 6  4x3oz, Customer Item: 504583, Packed by 3fish, Inc.
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-0043-2013·2012-10-17

    3fish Frozen Crab Bites Recalled for Listeria-Contaminated Onions

    3fish Inc. is recalling Frozen Crab Bites because they contain diced onions contaminated with Listeria monocytogenes.

    Product
    Frozen Crab Bites, ¿ oz, Bulk 100 x 0.5oz, Net Wt: 50 oz, Packed by 3fish, Inc.
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-0031-2013·2012-10-17

    Cut Fruit Express Recalls Mixed Fruit Cups Due to Salmonella Risk

    Cut Fruit Express, Inc. is recalling mixed fruit cups containing cantaloupe, honeydew, and grapes because the cantaloupe tested positive for Salmonella.

    Product
    CANTALOUPE, HONEY DEW, GRAPES (CHG) UNDER THE FOLLOWING BRANDS: USF 0811125 FRUIT MIX CHG RECEPTION 25# Manufactured by Cut Fruit Express Mpls., MN 55076. The following products Distributed By H. Brooks & Co. Mpls MN 55112: Festival Best of the Season Medley Fruit
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0041-2013·2012-10-17

    3fish Inc. Recalls HT Signature Lump Crab Cake Due to Listeria

    3fish Inc. is recalling HT Signature Lump Crab Cake because it was made with diced onions contaminated with Listeria monocytogenes.

    Product
    HT Signature Lump Crab Cake (Fresh), #81791, 4 oz @ 2x8ct, Net wt. 4 lbs, Packed by 3fish, Inc.
    Category
    Food
    Distribution
    2 states

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