The Recall Desk

Archive

November 2012 recalls

569 recalls were announced in November 2012.

What the numbers show

Critical
111
Severe
99
High
164
Moderate
162
Low
33

Of the 569 recalls this month scored against our rubric, 20% are Critical, 17% are Severe.

201–300 of 569

  • CriticalFDA (Food)·F-0676-2013·2012-11-21

    Advance Pierre Peanut Butter Sandwiches Recalled for Salmonella Contamination

    AdvancePierre Foods is recalling Pierre Peanut Butter & Strawberry Jam on White Bread sandwiches because they were made with peanut butter contaminated with Salmonella.

    Product
    Pierre Peanut Butter & Straw. Jam on White Bread, 2.80oz, AdvancePierre Foods, Inc., 9990 Princeton Glendale Road, Cincinnati, OH 45246.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0691-2013·2012-11-21

    Kentucky Rose Blue Cheese Recalled for Possible Listeria Contamination

    Kennys Farmhouse Cheese is recalling Kentucky Rose blue cheese due to possible Listeria monocytogenes contamination. The product was distributed in Kentucky, Tennessee, Florida, Illinois, Virginia, and Ohio.

    Product
    Kentucky Rose, blue cheese Sizes could be 8oz packages, 1.5lbs packages, 3.5lbs packages, 7lbs packages, or 15lb wheel Packaging could be vacuum packed bags, paper wrap, or plastic wrap
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·F-0687-2013·2012-11-21

    Dean Foods Recalls Western Family Ice Cream Due to Salmonella Ingredient

    Dean Foods is recalling Western Family Peanut Butter Cup ice cream because it was made with an ingredient previously recalled for Salmonella contamination.

    Product
    Western Family "Creamery Select" Premium Ice Cream Peanut Butter Cup, 1.5 QTS (1.42 L), (vanilla ice cream with peanut butter cup pieces, fudge swirl, and peanut butter ribbon)
    Category
    Food
    Distribution
    11 states
  • CriticalFDA (Food)·F-0671-2013·2012-11-21

    AdvancePierre Foods Recalls PB & Grape Jelly Wafers Due to Salmonella Risk

    AdvancePierre Foods is recalling PB & Grape Jelly on Whole Grain Graham Wafers because they were made with peanut butter contaminated with Salmonella.

    Product
    PB & Grape Jelly on Whole Grain Graham Wafers, AdvancePierre Foods, Inc., 9990 Princeton Glendale Road, Cincinnati, OH 45246.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0683-2013·2012-11-21

    Toft Dairy Recalls Prime Time Buckeye Bites Ice Cream Due to Salmonella Risk

    Toft Dairy Inc. is recalling Prime Time brand Buckeye Bites Ice Cream because it was manufactured using an ingredient recalled for Salmonella contamination.

    Product
    Prime Time brand Buckeye Bites Ice Cream in a paper carton 48 oz containers and 3 gallon tubs
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-0686-2013·2012-11-21

    Dean Foods Recalls Albertsons Peanut Butter Chocolate Ice Cream

    Dean Foods is recalling Albertsons Peanut Butter Chocolate Ice Cream because it was manufactured using an ingredient recalled for Salmonella contamination.

    Product
    Albertsons Peanut Butter Chocoate Ice Cream, 1.5 QTS (1.42 L), (chocolate ice cream with a peanut butter swirl)
    Category
    Food
    Distribution
    11 states
  • CriticalFDA (Food)·F-0685-2013·2012-11-21

    Dean Foods Recalls Albertsons Peanut Butter Cup Ice Cream

    Dean Foods is recalling Albertsons Peanut Butter Cup Ice Cream because it was made with an ingredient contaminated with Salmonella.

    Product
    Albertsons Peanut Butter Cup Ice Cream, 1.5 QTS (1.42 L)(vanilla ice cream with peanut butter cup pieces, fudge and peanut butter swirls)
    Category
    Food
    Distribution
    11 states
  • CriticalFDA (Food)·F-0673-2013·2012-11-21

    AdvancePierre Recalls Peanut Butter and Grape Jelly Cups Due to Salmonella

    AdvancePierre Foods is recalling specific lots of Pierre Peanut Butter & Grape Jelly Cups because they were made with peanut butter contaminated with Salmonella.

    Product
    Pierre Peanut Butter & Grape Jelly Cups., 1.50oz. and 2.80oz, AdvancePierre Foods, Inc., 9990 Princeton Glendale Road, Cincinnati, OH 45246.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0669-2013·2012-11-21

    Pierre On The Go PB Jamwich Grape Recalled Due to Salmonella Risk

    AdvancePierre Foods is recalling Pierre On The Go PB Jamwich Grape products because they were manufactured with peanut butter contaminated with Salmonella.

    Product
    Pierre On The Go PB Jamwich Grape, 2.00oz, Pierre On The Go PB Jamwich Grape, 2.00oz, AdvancePierre Foods, Inc., 9990 Princeton Glendale Road, Cincinnati, OH 45246.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0674-2013·2012-11-21

    AdvancePierre Peanut Butter & Straw Jam Recalled for Salmonella Risk

    AdvancePierre Foods is recalling Pierre Peanut Butter & Straw Jam on Whole Grain because it was made with peanut butter contaminated with Salmonella.

    Product
    Pierre Peanut Butter & Straw Jam on Whole Grain, 2.80oz, AdvancePierre Foods, Inc., 9990 Princeton Glendale Road, Cincinnati, OH 45246.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0663-2013·2012-11-21

    Pierre Peanut Butter & Jelly Squarewich Recalled for Salmonella Contamination

    AdvancePierre Foods is recalling Pierre Peanut Butter & Jelly Squarewich products because they were manufactured with peanut butter contaminated with Salmonella.

    Product
    Pierre Peanut Butter & Jelly Squarewich, 2.70oz., AdvancePierre Foods, Inc., 9990 Princeton Glendale Road, Cincinnati, OH 45246.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0667-2013·2012-11-21

    Market Day Peanut Butter & Jelly Grahamwich Recalled for Salmonella

    Market Day Peanut Butter & Jelly Grahamwich is being recalled because it was manufactured with peanut butter products contaminated with Salmonella.

    Product
    Market Day, Peanut Butter & Jelly Grahamwich, 12/2.20oz., Manufactured for: Market Day, Inc., Itasca, IL 60143.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0668-2013·2012-11-21

    AdvancePierre Recalls PB Jamwich Honey Due to Salmonella Contamination

    AdvancePierre Foods is recalling Pierre On The Go PB Jamwich Honey products because they were manufactured with peanut butter contaminated with Salmonella.

    Product
    Pierre On The Go PB Jamwich Honey, 2.00oz, AdvancePierre Foods, Inc., 9990 Princeton Glendale Road, Cincinnati, OH 45246.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0678-2013·2012-11-21

    AdvancePierre Recalls Peanut Butter and Strawberry Jam Sandwiches Due to Salmonella

    AdvancePierre Foods is recalling specific lots of Pierre On The Go peanut butter and strawberry jam sandwiches because they were made with peanut butter contaminated with Salmonella.

    Product
    Pierre On The Go Peanut Butter + Strawberry Jam, Jamwich, 2.00oz, AdvancePierre Foods, Inc., 9990 Princeton Glendale Road, Cincinnati, OH 45246.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0677-2013·2012-11-21

    Pierre Peanut Butter Jamwich Recalled Due to Salmonella Contamination

    AdvancePierre Foods is recalling Pierre Peanut Butter Jamwich & Banana on Whole Grain Bread because it was made with peanut butter contaminated with Salmonella.

    Product
    Pierre Peanut Butter Jamwich & Banana on Whole Grain Bread, 2.80oz., AdvancePierre Foods, Inc., 9990 Princeton Glendale Road, Cincinnati, OH 45246.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0656-2013·2012-11-21

    Sconza Candy Recalls Organic Toffee Peanuts Due to Salmonella Risk

    Sconza Candy Company is recalling organic toffee peanuts made with Sunland peanuts due to potential Salmonella contamination.

    Product
    Organic Toffee Peanuts;Bulk packaging - 20 pound cases; Ingredients: Organic Peanuts, Organic Sugar, Salt.
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-0672-2013·2012-11-21

    Pierre Peanut Butter Cups Recalled Due to Salmonella Contamination

    AdvancePierre is recalling Pierre Peanut Butter Cups because they were made with peanut butter contaminated with Salmonella.

    Product
    Pierre Peanut Butter Cup, 1.11oz., AdvancePierre, Inc., 9990 Princeton Glendale Road, Cincinnati, OH 462476.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0666-2013·2012-11-21

    AdvancePierre Peanut Butter and Jelly Sandwiches Recalled for Salmonella

    AdvancePierre Foods is recalling Pierre Peanut Butter & Strawberry Jelly on White sandwiches because they were made with peanut butter contaminated with Salmonella.

    Product
    Pierre Peanut Butter & Strawberry Jelly on White, 8/12PK, AdvancePierre Foods, Inc., 9990 Princeton Glendale Road, Cincinnati, OH 45246.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0660-2013·2012-11-21

    AdvancePierre Peanut Butter and Grape Jelly Sandwiches Recalled for Salmonella

    AdvancePierre Foods is recalling peanut butter and grape jelly sandwiches made with Sunland peanut butter contaminated with Salmonella.

    Product
    Pierre Peanut Butter & Grape Jelly on White Bread, 2.80oz, AdvancePierre Foods, Inc., 9990 Princeton Glendale Road, Cincinnati, OH 45246.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0282-2013·2012-11-21

    Terumo Sarns Modular Perfusion System 8000 Recalled for Monitor Malfunctions

    Terumo CVS is recalling 466 Sarns Modular Perfusion System 8000 units due to arterial and cardioplegia monitor malfunctions, including power issues and inaccurate pressure alarms.

    Product
    Perfusion System 8000, base 4 pump, 220V/240V safety monitor included The Sarns" Modular Perfusion System 8000 is indicated for use for up to 6 hours on the extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures, w
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0284-2013·2012-11-21

    Terumo Sarns Modular Perfusion System 8000 Recalled for Monitor Malfunctions

    Terumo CVS is recalling 26 Sarns Modular Perfusion System 8000 units due to reported malfunctions in arterial and cardioplegia monitors, including power issues and inaccurate pressure alarms.

    Product
    Perfusion System 8000, base 4 pump, 100V safety monitor included The Sarns" Modular Perfusion System 8000 is indicated for use for up to 6 hours on the extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures, when u
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0285-2013·2012-11-21

    Terumo Sarns Modular Perfusion System 8000 Recalled for Monitor Malfunctions

    Terumo CVS is recalling 81 Sarns Modular Perfusion System 8000 units due to arterial and cardioplegia monitor malfunctions, including power issues and inaccurate pressure alarms.

    Product
    Perfusion System 8000, base 5 pump, 100V safety monitor included The Sarns" Modular Perfusion System 8000 is indicated for use for up to 6 hours on the extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures, when u
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-052-2013·2012-11-21

    Sterile Products from New England Compounding Center Recalled Due to Sterility Concerns

    New England Compounding Center is recalling all of its sterile products because the company cannot assure that the products are sterile.

    Product
    All Sterile Products manufactured by NECC (New England Compounding Center), Framingham, MA. A complete list of products can be found on their website at www.neccrx.com
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-053-2013·2012-11-21

    New England Compounding Center Recalls Non-Sterile Products Due to GMP Deviations

    New England Compounding Center is voluntarily recalling all non-sterile products due to Good Manufacturing Practice (GMP) deviations. The recall covers products distributed nationwide and in Japan.

    Product
    All Non Sterile Products manufactured by NECC (New England Compounding Center), Framingham, MA. A complete list of products can be found on their website at www.neccrx.com
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0692-2013·2012-11-21

    Kentucky Blue Bleu Cheese Recalled for Possible Listeria Contamination

    Kennys Farmhouse Cheese is recalling Kentucky Blue bleu cheese due to possible Listeria monocytogenes contamination. The product was distributed in six states.

    Product
    Kentucky Blue, bleu cheese Sizes could be 8oz packages, 1.5lbs packages, 3.5lbs packages, 7lbs packages, or 15lb wheel Packaging could be vacuum packed bags, paper wrap, or plastic wrap
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0689-2013·2012-11-21

    B.T. McElrath Peanut Butter Pave Recalled for Salmonella Risk

    B.T. McElrath Chocolatier is recalling Peanut Butter Pave products due to potential Salmonella contamination. The recall affects specific lots distributed in seven states.

    Product
    Peanut Butter Pave, UPC code 693868102117 & 69386905312, in the following sizes: 1) 5 Piece Peanut Butter Pave, 63 Grams per pack, 12 Packs per case. 2) 2 Piece Peanut Butter Pave, 26 Grams per pack, 10 Packs per case. 3) Bulk Peanut Butter Pave, 415 Grams per pack.
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·F-0679-2013·2012-11-21

    Iskream Peanut Butter and Jelly Ice Cream Recalled for Salmonella Risk

    Bucks Ice Cream is recalling Iskream brand Peanut Butter and Jelly ice cream because it was manufactured with Sunland recalled peanut butter, posing a potential salmonella contamination risk.

    Product
    Iskream brand Peanut Butter and Jelly No Sugar Added, reduced fat, packaged in Pint (retail) an 2.5 gallon bulk cartons
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0693-2013·2012-11-21

    Kennys Farmhouse Cheese Recalls Awe Brie for Listeria Risk

    Kennys Farmhouse Cheese is recalling Awe Brie cheese due to possible Listeria monocytogenes contamination. The product was distributed in Kentucky, Tennessee, Florida, Illinois, Virginia, and Ohio.

    Product
    Awe Brie Sizes could be 8oz packages, 1.5lbs packages, 3.5lbs packages, 7lbs packages, or 15lb wheel Packaging could be vacuum packed bags, paper wrap, or plastic wrap
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Drugs)·D-054-2013·2012-11-21

    Ameridose Recalls All Sterile Products Due to Sterility Assurance Concerns

    Ameridose LLC is recalling all sterile products manufactured in Westborough, MA, due to a lack of assurance of sterility. The recall is nationwide and includes all lot codes within expiry.

    Product
    All Sterile Products manufactured by Ameridose LLC, Westborough, MA. A complete list of all products subject to this recall can be accessed on-line at www.ameridose.com
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0703-2013·2012-11-21

    FreshPoint South Florida Recalls Fresh Cut Mango Products

    FreshPoint South Florida is recalling fresh cut mango products due to a voluntary recall initiated by Coast Citrus Distributors.

    Product
    Fresh Mango peeled and cut into cubes, slices, or halves labeled as listed: ***Fresh Point***Fresh Cuts***Food Service Fruit Mango PLD Cubed 1/2***2 x 5lb Tray***Net Wt. 310 lb.*** ***Fresh Point***Fresh Cuts***Food Service Fruit Mango Peeled / Halved***2 X 2.5 lb Tray***Net Wt
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0659-2013·2012-11-21

    Super Store Industries Recalls Ice Cream Due to Salmonella Risk

    Super Store Industries is recalling SCOOPFUL Churned Light Ice Cream because a raw material supplier was recalled for potential Salmonella contamination.

    Product
    Ice Cream - label reads in part "*** Lovin' SCOOPFUL CHURNED LIGHT ICE CREAM *** SUPER DUPER PEANUT BUTTER CUP***
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-0694-2013·2012-11-21

    Kennys Farmhouse Cheese Recalls Tomme de Nena for Listeria Risk

    Kennys Farmhouse Cheese is recalling Tomme de Nena cheese due to possible Listeria monocytogenes contamination. The product was distributed in six states.

    Product
    Tomme de Nena Sizes could be 8oz packages, 1.5lbs packages, 3.5lbs packages, 7lbs packages, or 15lb wheel Packaging could be vacuum packed bags, paper wrap, or plastic wrap
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0702-2013·2012-11-21

    Coast Citrus Recalls Kent's and Keitt's Mangoes Packed at Agricola Daniella

    Coast Citrus Distributors is voluntarily recalling Kent's and Keitt's mangoes packed at Agricola Daniella. The recall involves specific mango products distributed in the US and Caribbean.

    Product
    ***Fresh Point***Fresh Cuts***Retail Mango Sliced***6 X 8oz Cups Packages***Net Wt. 27 lb.***
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0700-2013·2012-11-21

    Coast Citrus Recalls Kent's and Keitt's Mangos Packed by Agricola Daniella

    Coast Citrus Distributors is voluntarily recalling Kent's and Keitt's mangos packed by Agricola Daniella due to a product recall.

    Product
    ***Fresh Point***Fresh Cuts***Fruit Mango/Papaya Diced***2 x 5lb Tray***Net. Wt. 10 lb.***
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·12V548000·2012-11-21

    Honda Recalls 2012 Civic Vehicles Due to Incorrect Steering Column Assembly

    Honda is recalling 2012 Civic vehicles manufactured in late October 2012 because they were assembled with incorrect steering columns that may lack proper energy-absorbing characteristics.

    Product
    HONDA — HONDA CIVIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V546000·2012-11-21

    Navistar Recalls 2012-2013 International Trucks Due to Brake Bracket Fracture Risk

    Navistar is recalling 2012-2013 International ProStar and TranStar trucks because front brake bracket assemblies may fracture, potentially causing brake failure and increased crash risk.

    Product
    INTERNATIONAL — INTERNATIONAL TRANSTAR, PROSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0682-2013·2012-11-21

    Zatarain's Chicken Flavor Rice Mix Recalled for Undeclared Wheat

    McCormick & Company is recalling Zatarain's New Orleans Style Chicken Flavor Rice Mix because the product contains wheat but the label does not declare it.

    Product
    Zatarain's New Orleans Style Chicken Flavor Rice Mix, Item No. Z09705, packaged in 6.3 oz boxes, 12 boxes per carton, Box UPC: 7142901001
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0681-2013·2012-11-21

    Zatarain's Beef Flavor Rice Mix Recalled for Undeclared Wheat

    McCormick & Company is recalling Zatarain's New Orleans Style Beef Flavor Rice Mix because the product contains wheat but the label does not declare it.

    Product
    Zatarain's New Orleans Style Beef Flavor Rice Mix, packaged in 6.8 oz boxes, 12 boxes per carton, Box UPC: 7142901001
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0684-2013·2012-11-21

    Whole Foods Shrimp Stir Fry Recalled for Undeclared Tree Nuts

    Whole Foods Market is recalling 164 units of Shrimp Stir Fry because the label fails to declare tree nuts (almond and cashews). The product was sold in Massachusetts, Connecticut, New York, and New Jersey.

    Product
    Whole Foods Meal Shrimp Stir Fry, 16 oz plastic container, Refrigerated, Product Code 3640630222
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0658-2013·2012-11-21

    Aunt Marie's Bakery Cookie Dough Recalled for Foreign Object

    RDK Corp is recalling Aunt Marie's Bakery Gourmet Cookie Dough due to a foreign object hazard. The product was distributed to fund-raising organizations in Arizona, Illinois, and Wisconsin.

    Product
    Aunt Marie's Bakery Gourmet Cookie Dough, Chocolate Chunk, packaged in 3-lb. plastic tubs. Distributed by Racine Danish Kringles, Racine, WI.
    Category
    Food
    Distribution
    3 states
  • HighCPSC·13707·2012-11-21

    Hunter Douglas Recalls Custom Cellular and Pleated Window Coverings for Strangulation Hazard

    Hunter Douglas is recalling about 4,400 custom cellular and pleated window coverings because a knot in the cord stop may prevent it from breaking away, creating a strangulation risk for children.

    Product
    Standard cordlock top-down/bottom-up Duette and Applause honeycomb shades; standard cordlock top-down/bottom-up Hunter Douglas pleated shades; Hunter Douglas Brilliance Privacy View pleated shades and standard cordlock Duette and Applause Duolite shades
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0680-2013·2012-11-21

    Taco Loco Salmon Wrap Recalled for Undeclared Soy Allergen

    Taco Loco Products Inc is recalling Salmon Wraps because the product contains soy oil and soy, which were not declared on the label.

    Product
    Salmon Wrap. Two wraps per package. Net Wt 8 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0688-2013·2012-11-21

    Publix Recalls Frozen Tempura Shrimp for Undeclared Soy Allergen

    Publix recalled frozen tempura shrimp because a dipping sauce packet containing undeclared soy was included in the box.

    Product
    Frozen Publix Brand Premium Tempura Shrimp, 11 oz box packed 10 boxes per case.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-0287-2013·2012-11-21

    Dako PT Link Waterbath Recalled for Electrical Shock Hazard

    Dako North America Inc. is recalling 136 PT Link Waterbath units due to a potential electrical shock hazard if the heater pad becomes wet.

    Product
    PT Link Waterbath, Model#PT100. Lab Vision PT Module Plus provides an automated standarized alternative to labor intensive and time consuming dewaxing and epitote retrieval procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0283-2013·2012-11-21

    Terumo Sarns Modular Perfusion System 8000 Recalled for Monitor Malfunctions

    Terumo CVS is recalling 312 Sarns Modular Perfusion System 8000 units due to reported malfunctions in arterial and cardioplegia monitors, including power issues and inaccurate pressure alarms.

    Product
    Perfusion System 8000, base 5 pump, 220V/240V safety monitor included The Sarns" Modular Perfusion System 8000 is indicated for use for up to 6 hours on the extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures, w
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0690-2013·2012-11-21

    Mazzio's Marinara Sauce Recalled for Undeclared Milk Allergen

    Paradise Tomato Kitchens Inc is recalling Mazzio's Marinara Sauce because the ingredient statement fails to declare milk as the source of butter.

    Product
    Mazzio's Marinara Sauce, 6.65-lb pouch, 6 pouches per case Pouches are packed in cardboard box for shipment
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0294-2013·2012-11-21

    MOOG Recalls EnteraLite Infinity Enteral Feeding Pumps Due to Voltage Defect

    MOOG Medical Devices Group is voluntarily recalling specific EnteraLite Infinity enteral feeding pumps because a PCB defect may cause the device to shut down.

    Product
    EnteraLite Infinity Enteral Feeding Pump identified with the following list numbers: INFKIT2 and INFORNG. The device is used with disposable PVC administration tubing sets to provide a means for the volumetric delivery of fluids used in enteral applications. The EnteraLite In
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0280-2013·2012-11-21

    Terumo Recalls Sarns Modular Perfusion System 8000 Due to Monitor Malfunctions

    Terumo CVS is recalling 274 Sarns Modular Perfusion System 8000 units due to reported malfunctions in arterial and cardioplegia monitors, including power issues and inaccurate pressure alarms.

    Product
    Perfusion System 8000, base 4 pump, 115V safety monitor included The Sarns" Modular Perfusion System 8000 is indicated for use for up to 6 hours on the extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures, when u
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0286-2013·2012-11-21

    Stryker Recalls Peri-Acetabular Prosthesis Femoral Extension Components

    Stryker Howmedica Osteonics is recalling 301 units of Peri-Acetabular Prosthesis V40 Femoral Extension Components due to insufficient taper torsional strength when used with forged CoCr stems.

    Product
    Special Orthopaedic Solution Peri-Acetabular Prosthesis V40 Femoral Extension Component Product Usage: The PAR extension piece is a component of the PAR assembly. The Peri-Acetabular Reconstruction (PAR) endoprosthesis was developed to meet the unique needs of patients who
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0281-2013·2012-11-21

    Terumo Sarns Modular Perfusion System 8000 Recalled for Monitor Malfunctions

    Terumo CVS is recalling Sarns Modular Perfusion System 8000 units due to reported malfunctions in arterial and cardioplegia monitors, including power issues and inaccurate pressure alarms.

    Product
    Perfusion System 8000, base 5 pump, 115V safety monitor included The Sarns" Modular Perfusion System 8000 is indicated for use for up to 6 hours on the extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures, when u
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0278-2013·2012-11-21

    Terumo HX2 Temperature Management System Recalled for Board Defects

    Terumo is recalling 19 HX2 Temperature Management Systems because AC Control boards were manufactured with incorrect flux, which may cause premature failure.

    Product
    HX2 Temp Manage SYS 120V The Terumo HX2 Temperature Management System is a selfcontained, dual channel system for supplying temperature controlled water to heat exchangers used in an extracorporeal circuit.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0279-2013·2012-11-21

    Terumo HX2 Temperature Management System Recalled for Board Defect

    Terumo is recalling 15 HX2 Temperature Management Systems because AC Control boards were manufactured with incorrect flux, which may cause premature failure.

    Product
    Tested AC Control BD, 120V, X2 The Terumo HX2 Temperature Management System is a selfcontained, dual channel system for supplying temperature controlled water to heat exchangers used in an extracorporeal circuit.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0288-2013·2012-11-21

    Trivascular Recalls Fill Polymer Kits Due to Potential Stopcock Leaks

    Trivascular is recalling 41 units of Fill Polymer Kits in European distributor inventory due to potential stopcock cracks that may cause leaks.

    Product
    TriVascular brand Fill Polymer Kit, Endovascular Graft, Aneurysm Treatment System, European Model Number: TVFP14-B, (in European distributor inventory only); PRODUCT Usage: The TriVascular Ovation Abdominal Stent Graft System is indicated in subjects diagnosed with an aneu
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0296-2013·2012-11-21

    Zimmer Recalls ATS 3000 Tourniquets Due to Counterfeit Chip Failures

    Zimmer is voluntarily removing 204 ATS 3000 Automatic Tourniquet Systems worldwide after complaints of failures caused by counterfeit chips.

    Product
    ATS 3000 Automatic Tourniquet System w/HOSES AND LOP SENSOR Intended to be used by qualified medical professionals to temporarily occlude blood flow in a patient's extremities during surgical procedures on those extremities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0698-2013·2012-11-21

    Zatarain's Chicken and Cheddar Broccoli Mix Recalled for Undeclared Wheat

    McCormick & Company is recalling Zatarain's Chicken/Cheddar Broccoli Mix because the product contains wheat but the label does not declare it.

    Product
    Zatarain's Chicken/Cheddar Brocolli Mix, Item Number: 900108337, a combination pack containing, 6.3 oz boxes of New Orleans Style Chicken Flavor Rice Mix and Cheddar Broccolli Mix.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0701-2013·2012-11-21

    FreshPoint Fresh Cuts Salsa Mango and Papaya Recalled for Foreign Material

    FreshPoint South Florida is recalling Fresh Cuts Salsa Mango and Papaya due to a foreign material hazard. The product was distributed in Florida, New Jersey, and several Caribbean territories.

    Product
    ***Fresh Point***Fresh Cuts***Salsa Mango and Papaya*** 2 x 5lb Tray***Net Wt. 10 lb.***
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0657-2013·2012-11-21

    American Vines Black Soft Licorice Twists Recalled for Lead Contamination

    American Licorice Co is recalling specific lots of American Vines Black Soft Licorice Twists due to elevated lead levels found during internal sampling.

    Product
    American Vines band Natural Vines Black Soft Licorice Twists; All Natural Ingredients, 8 oz (226g), No Preservatives, Product is processed and packaged by American Licorice Company, Union City, CA; Displays and Pallets info: ----6 ct. Case, Item: #8483, Case UPC:
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-055-2013·2012-11-21

    Ameridose Recalls Non-Sterile Drug Products Due to GMP Deficiencies

    Ameridose LLC is voluntarily recalling all non-sterile products nationwide due to Good Manufacturing Practice (GMP) deficiencies. The recall was initiated in October 2012.

    Product
    All Non-Sterile Products manufactured by Ameridose LLC, Westborough, MA. A complete list of all products subject to this recall can be accessed on-line at www.ameridose.com
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0277-2013·2012-11-21

    Synthes External Fixation Clamp Recalled for Incorrect MR Safety Labeling

    Synthes USA HQ, Inc. is recalling 8 units of External Fixation System Tube to Tube Clamps because the provided insert incorrectly states the product is MR safe, while the device is actually MR Conditional.

    Product
    Synthes External Fixation System Tube to Tube Clamp, Part Number 390.007. Intended for use to provide treatment for long bone and pelvic fractures that require external fixation. Specifically, the components can be used for: Stabilization of soft tissues and fractures; Polytra
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0276-2013·2012-11-21

    Progressive Medical Recalls Endoscopic Dissectors with Broken Sterile Seals

    Progressive Medical Inc. is recalling 70 boxes of PMI Endoscopic Dissectors because some sterile packages had broken seals, potentially compromising sterility.

    Product
    Progressive Medical PMI Endoscopic Dissector with Kittner Tip (5mm x 40cm), Reorder Number: PMILK40, Product Sterile in Unopened/Undamaged pouch, Cotton Tip - X-Ray Detectable, 1 Pc/Pouch, 10 Pouches/Box, 20 boxes/case. Exclusively Distributed in the U.S. Market by: Progressive
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-050-2013·2012-11-21

    Stat Rx USA Recalls Tobramycin Ophthalmic Ointment Due to Labeling Error

    Stat Rx USA is recalling 22 units of Tobramycin Ophthalmic Ointment because the labels incorrectly identify the product as an ointment instead of a solution.

    Product
    Tobramycin Ophthalmic Oint., 0.3%, 5ml bottle, (Generic for: Tobrex), Rx only, Sterile, Mfg By Akorn, Inc., Lake Forest, IL 60045, NDC 16590-224-05,
    Category
    Drug
    Distribution
    3 states
  • LowFDA (Drugs)·D-051-2013·2012-11-21

    Stat Rx USA Recalls Venlafaxine ER Due to Labeling Error

    Stat Rx USA is recalling 5 bottles of Venlafaxine ER 150mg because the label incorrectly identifies the dosage form as 'Tabs' instead of 'Capsules.'

    Product
    Venlafaxine ER 150mg, 30 Tabs bottle, Generic for: Effexor, Packaged and Distributed by: Stat Rx USA, LLC, Gainesville, GA 30501 NDC 42549-684-30
    Category
    Drug
    Distribution
    2 states
  • LowFDA (Devices)·Z-0295-2013·2012-11-21

    Gulf South Medical Supply Recalls Vinyl Exam Gloves Shipped Before Customs Clearance

    Gulf South Medical Supply is recalling Select Medical Products Vinyl Powder-Free Exam Gloves because they were shipped before U.S. Customs cleared them for sale.

    Product
    Select Medical Products Vinyl Powder-Free Exam Gloves, Medium Model # 6370 and Large Model # 6371, 100 per box; 10 boxes per case. Usage: Patient Examination.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-056-2013·2012-11-21

    ITW Dymon Recalls Lemon Hand Sanitizing Wipes for CGMP Deviations

    ITW Dymon is recalling specific lots of Lemon Hand Sanitizing Wipes because they were manufactured with raw material containing unknown particles believed to be water and dirt.

    Product
    Lemon Hand Sanitizing Wipes [n-alkyl dimethyl benzyl ammonium chloride (0.1%) and n-alkyl dimethyl ethyl benzyl ammonium chloride (0.1%)], labeled as a) Genuine Joe Cleaning Supplies, Lemon Scent, Anti-microbial Hand Sanitizing Wipes, 120-count premoistened wipes per bucket, 6 bu
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0289-2013·2012-11-21

    Horiba Medical Recalls ABX PENTRA Creatinine 120 CP Reagent

    Horiba Medical is recalling ABX PENTRA Creatinine 120 CP reagent because a calibration alarm prevents the assay from being used.

    Product
    ABX PENTRA Creatinine 120 CP, Model Number Creatinine Part # A11A01868, Lot Numbers: 203273706, 203273707, 203273808, 203273709. The ABX PENTRA Creatinine 120 CP is an in vitro diagnostic assay for the quantitative determination of creatinine in human serum, plasma and urine ba
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V541000·2012-11-20

    Starcraft Recalls 2013 Autumn Ridge AR-One Travel Trailers for Wiring Defect

    Starcraft is recalling 22 model year 2013 Autumn Ridge AR-One travel trailers because loose electrical wiring connections could cause excessive heat, leading to fire, injury, or death.

    Product
    STARCRAFT — STARCRAFT AUTUMN RIDGE AR-ONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·12V538000·2012-11-15

    Blue Bird Recalls 2013-2014 Vision School Buses Due to Brake Light Defect

    Blue Bird is recalling 452 model year 2013 and 2014 Vision school buses equipped with Ford 6.8L propane engines because the brake light switch may malfunction, increasing crash risk.

    Product
    BLUE BIRD — BLUE BIRD VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·12V539000·2012-11-15

    Volvo Bus 9700 Recalled for Wheelchair Lift Safety Pin Defects

    Prevost is recalling 44 Volvo Bus 9700 coaches because missing or inoperable wheelchair lift safety pins may prevent safe stowing, increasing injury risk.

    Product
    VOLVO BUS — VOLVO BUS 9700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·12V540000·2012-11-15

    Volkswagen Recalls 2012-2013 Beetles for Airbag Sensor Defect

    Volkswagen is recalling 2012-2013 Beetles with leather sport seats because a wet seat may prevent the airbag from turning off, increasing injury risk for children.

    Product
    VOLKSWAGEN — VOLKSWAGEN BEETLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·13040·2012-11-15

    Kawasaki Recalls Lawn Mower Engines Due to Fuel Leak Fire Hazard

    Kawasaki Motors is recalling about 210,000 lawn mower engines because the fuel filter can leak, posing a fire hazard. No injuries have been reported.

    Product
    Lawn Mower Engines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·13041·2012-11-15

    Kawasaki Recalls Lawn Mower Fuel Filters Due to Fire Hazard

    Kawasaki Motors is recalling fuel filters and tune-up kits for lawn mowers and utility vehicles because the filters can leak fuel, posing a fire hazard.

    Product
    Fuel Filters and Tune-Up Kits with Fuel Filters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·13706·2012-11-15

    John Deere Recalls Utility Vehicles Due to Fuel Filter Fire Hazard

    John Deere is recalling about 4,340 Gator utility vehicles with Kawasaki engines because the fuel filter can leak, posing a fire hazard. No injuries have been reported.

    Product
    Utility Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0653-2013·2012-11-14

    Green & Black's Organic Peanut Chocolate Bar Recalled for Salmonella Risk

    Mondelez Global is recalling Green & Black's Organic Peanut & Sea Salt Milk Chocolate Bars because the peanuts may be contaminated with Salmonella.

    Product
    Green & Black's Organic Peanut & Sea Salt Milk Chocolate Bar NET WT. 3.5 oz (100g). UPC 708656 100562.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0615-2013·2012-11-14

    Dole American Blend Salad Recalled Due to Listeria Monocytogenes Detection

    Dole Fresh Vegetables is recalling Dole American Blend salad because a random sample tested positive for Listeria Monocytogenes.

    Product
    Dole American Blend; Iceberg, Romaine, Red Cabbage, Carrots and Radishes. Net Wt. 12 oz. (340g) UPC 0 71430 00933 8 Distributed by Dole Fresh Vegetables, Monterey, CA 93940
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0624-2013·2012-11-14

    Think Thin Nutrition Bars Recalled for Potential Salmonella Contamination

    Think Thin, LLC is recalling Crunch thinkThin White Chocolate Dipped Mixed Nuts bars because they may contain peanuts contaminated with Salmonella.

    Product
    Nutrition bar. Crunch¿ thinkThin Brand, White Chocolate Dipped Mixed Nuts, 40 grams. Packaged in plastic, labeled as:"Distributed by thinkproducts***Ventura, CA 93003***". 10 bars/carton, 12 cartons/case. 120 bars per case
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0613-2013·2012-11-14

    Ridgebar Peanut Butter Crunch Nutrition Bar Recalled for Salmonella Risk

    Creative Energy Foods is recalling Ridgebar Peanut Butter Crunch bars because they contain peanuts from Sunland, Inc., which are under recall for potential Salmonella contamination.

    Product
    Ridgebar Peanut Butter Crunch, 40 grams
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-0626-2013·2012-11-14

    Think Thin Nutrition Bars Recalled for Potential Salmonella Contamination

    Think Thin, LLC is recalling Crunch thinkThin nutrition bars that may contain peanuts contaminated with Salmonella.

    Product
    Nutrition bar. Crunch¿ thinkThin Brand, Caramel Chocolate Dipped Mixed Nuts, 40 grams. Packaged in plastic, labeled as:"Distributed by thinkproducts***Ventura, CA 93003***". 10 bars/carton, 12 cartons/case. 120 bars per case
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0610-2013·2012-11-14

    Kent's and Keitt's Brand Mangoes Recalled Due to Salmonella Risk

    Coast Citrus Distributors is voluntarily recalling Kent's and Keitt's brand mangoes packed at Agricola Daniella due to salmonella associated with the producer.

    Product
    Fruit Mango Peeled and Sliced, Ready To Eat Product, 2, 5-lb Trays per case
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-0618-2013·2012-11-14

    Su-Nun Crushed Roasted Thai Red Pepper Recalled for Salmonella

    S & P Company Limited is recalling Su-Nun Crushed Roasted Thai Red Pepper due to positive Salmonella results found during FDA routine import sampling.

    Product
    Su-Nun Crushed Roasted Thai Red Pepper, 10.58 oz. 12 jars/case. Packaged in clear plastic jars, red plastic screw on lid, with a red and yellow label. The principal display label has a red background with a yellow oval that reads in part:"SU-NUN***BRAND***HOT***CRUSHED ROASTED TH
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-0596-2013·2012-11-14

    Clemmy's Peanut Butter Chocolate Chip Ice Cream Recalled for Salmonella Risk

    Clemmy's LLC is recalling Peanut Butter Chocolate Chip Ice Cream because the peanut butter ingredient may be contaminated with Salmonella.

    Product
    Clemmy's Brand Peanut Butter Chocolate Chip Ice Cream, Pint Size, 16 OZ (437mL), UPC 8 94509 00231 9. Labeling reads in part: "CLEMMY'S RICH AND CREAMY PEANUT BUTTER CHOCOLATE CHIP*** 100% SUGAR FREE LACTOSE FREE GLUTEN FREE, 16 OZ (473mL)***DIST BY: Clemmy's Ice Cream P.O.Box 17
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0651-2013·2012-11-14

    Belfonte Home Run Sundae Ice Cream Recalled for Salmonella Risk

    Belfonte Ice Cream & Dairy Foods Co is recalling Home Run Sundae Ice Cream because the peanut butter base may be contaminated with Salmonella.

    Product
    Belfonte Home Run Sundae Ice Cream, A Baseball Nut Blend of Chocolate Peanuts, Chocolate Coated Pretzels, and a Thick Fudge Swirl in Peanut Butter/Chocolate Ice Cream, 56 oz. (1.66L) Belonite Ice Cream Company, Kansas City, MO
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-0608-2013·2012-11-14

    Kent's and Keitt's Brand Mangoes Recalled Due to Salmonella Risk

    Coast Citrus Distributors is recalling Kent's and Keitt's brand mangoes packed at Agricola Daniella due to salmonella associated with the producer.

    Product
    Fruit Mango Whole Peeled, Ready-To-Eat Product, 2, 5-LB Trays per case
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-0598-2013·2012-11-14

    Luna & Larry's Coconut Bliss Chocolate Peanut Butter Dessert Recalled for Salmonella Risk

    Bliss Unlimited is recalling Luna & Larry's Organic Coconut Bliss Chocolate Peanut Butter Non-Dairy Frozen Dessert because the peanut butter ingredient may be contaminated with Salmonella.

    Product
    Chocolate Peanut Butter Non-Dairy Frozen Dessert is sold under brand Luna & Larry's Organic Coconut Bliss. It is packaged in One Pint (473ml) StanPac paperboard container, 8 cups per case. The UPC code 8 96767 00121 9. The product is labeled in parts: "***CHOCOLATE PEANUT BU
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·F-0625-2013·2012-11-14

    Think Thin Nutrition Bars Recalled for Potential Salmonella Contamination

    Think Thin, LLC is recalling Crunch thinkThin nutrition bars that may contain peanuts contaminated with Salmonella.

    Product
    Nutrition bar. Crunch¿ thinkThin Brand, Chocolate Dipped Mixed Nuts, 40 grams. Packaged in plastic, labeled as:"Distributed by thinkproducts***Ventura, CA 93003***". 10 bars/carton, 12 cartons/case. 120 bars per case
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0636-2013·2012-11-14

    Jamba Juice Peanut Butter Smoothie Recalled Due to Salmonella Risk

    Jamba Juice is recalling Peanut Butter Moo'd Smoothies because they were made with peanut butter potentially contaminated with Salmonella.

    Product
    Jamba Juice brand Peanut Butter Moo'd Smoothie; All sizes (small, medium, large); A Blend Of: Nonfat Vanilla Yogurt (Contains Milk), Chocolate Moo'd Base (Contains Milk), Soymilk (Contains Soy), Ice, Bananas, Peanut Butter (Contains Peanuts); The product is processed and packaged
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-0635-2013·2012-11-14

    Giant Eagle Recalls Mango Medley Fruit Cups for Salmonella Risk

    Giant Eagle is recalling 16 oz Mango Medley fruit cups due to possible Salmonella contamination in the mangoes used in production.

    Product
    Mango Medley, 16 oz (contains cantaloupe, honeydew, mango, grapes), distributed by Fresh Food Mfg, 2500 Love Road, Freedom, PA 15042, UPC 3003430338 (4 -16 oz clear plastic containers per case)
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-0599-2013·2012-11-14

    Fresh Express Hearts of Romaine Recalled Due to Salmonella Contamination

    Fresh Express is recalling 18 oz Hearts of Romaine packages because samples tested positive for Salmonella. The product was distributed in 11 states and Canada.

    Product
    Fresh Express, Hearts of Romaine, 18 oz, Fresh Express Incorporated, packed in clear flexible plastic package.
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0617-2013·2012-11-14

    Trifecta Foods Recalls Sunland Peanuts Due to Salmonella Contamination Risk

    Trifecta Foods is voluntarily recalling in-shell roasted peanuts supplied by Sunland, Inc. because they may be contaminated with Salmonella.

    Product
    Peanuts in Shell, R Unsalted, 8oz, Item#305, 12pk/case, UPC 070334003053. Peanuts in Shell, R Unsalted, 8oz, Item#308, 36pk/case, UPC 070334003053. Peanuts in Shell, R Unsalted, 16oz, Item#318, 24pk/case, UPC 070334003189. Peanuts in Shell, R Unsalted-Display Ready, 8oz, Item#
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0623-2013·2012-11-14

    Think Thin Nutrition Bars Recalled for Potential Salmonella Contamination

    Think Thin, LLC is recalling Crunch thinkThin Mixed Nuts nutrition bars because they may contain peanuts contaminated with Salmonella.

    Product
    Nutrition bar. Crunch¿ thinkThin Brand, Mixed Nuts, 40 grams. Packaged in plastic, labeled as:"Distributed by thinkproducts***Ventura, CA 93003***". 10 bars/carton, 12 cartons/case. 120 bars per case
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0629-2013·2012-11-14

    Think Thin Nutrition Bars Recalled for Potential Salmonella Contamination

    Think Thin, LLC is recalling Crunch thinkThin nutrition bars that may contain peanuts contaminated with Salmonella.

    Product
    Nutrition bar. Crunch¿ thinkThin Brand, Cranberry Apple & Mixed Nuts, 40 grams. Packaged in plastic, labeled as:"Distributed by thinkproducts***Ventura, CA 93003***". 10 bars/carton, 12 cartons/case. 120 bars per case
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0597-2013·2012-11-14

    PureFit Peanut Butter Bars Recalled for Possible Salmonella Contamination

    PureFit Inc. is recalling Peanut Butter Crunch Bars because the peanut butter supplied by Sunland Inc. may be contaminated with Salmonella.

    Product
    PureFit Peanut Butter Bars, size 2 oz (56.7g) and box of 15 bars in 1 box/carton. UPC 812787001008, 812787002005
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0620-2013·2012-11-14

    Velvet Buckeye Classic Ice Cream Recalled for Potential Salmonella Contamination

    Velvet Ice Cream Company is recalling Buckeye Classic ice cream because it was made with peanut butter potentially contaminated with Salmonella.

    Product
    Velvet Buckeye Classic MFD BY VELVET ICE CREAM CO., INC UTICA, OHIO 43080 1-800-589-5000 56 oz (UPC #70682-10038), 3 gallon (UPC #70682-10519) and pints (UPC #70682-10423)
    Category
    Food
    Distribution
    4 states

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