The Recall Desk

Archive

June 2012 recalls

351 recalls were announced in June 2012.

What the numbers show

Critical
12
Severe
110
High
152
Moderate
65
Low
12

Of the 351 recalls this month scored against our rubric, 3% are Critical, 31% are Severe.

201–300 of 351

  • SevereNHTSA·12V288000·2012-06-22

    GM Recalls 2011-2012 Chevrolet Cruze Vehicles for Engine Fire Risk

    General Motors is recalling 2011 and 2012 Chevrolet Cruze vehicles because spilled oil may ignite near hot engine parts, posing a fire hazard.

    Product
    CHEVROLET — CHEVROLET CRUZE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V290000·2012-06-22

    Tracker Marine Recalls Trailstar Boat Trailers Due to Brake Failure Risk

    Tracker Marine is recalling certain 2012-2013 Trailstar boat trailers because a weld defect can cause brake overheating and failure, increasing crash risk.

    Product
    TRAILSTAR — TRAILSTAR TAHOE Q5, TAHOE Q7, TAHOE Q8, TAHOE 195
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V291000·2012-06-22

    Vermeer R9X12T Trailer Recalled for Brake Clearance Defect

    Vermeer is recalling 2010-2012 R9X12T trailers because inadequate clearance between the slack adjuster arm and frame can bend the arm, reducing braking capacity.

    Product
    VERMEER — VERMEER R9X12T
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V289000·2012-06-22

    GM Recalls 2011-2012 Chevrolet Cruze for Fuel Tank Weld Defect

    General Motors is recalling 2011-2012 Chevrolet Cruze vehicles because missing welds on fuel tank brackets could allow the tank to come loose in a crash, potentially causing a fuel leak and fire.

    Product
    CHEVROLET — CHEVROLET CRUZE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·12V292000·2012-06-22

    Molly Trolley Recalls Two Vehicles Due to Wheelchair Lift Latch Defect

    Molly Corporation is recalling two 2010 Molly Trolley vehicles because wheelchair lift latches may bend, allowing occupants to fall from an elevated platform.

    Product
    MOLLY TROLLEY — MOLLY TROLLEY MOLLY TROLLEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·12V293000·2012-06-22

    Starcraft Buses Recalled for Wheelchair Lift Roll Stop Latch Defect

    Starcraft is recalling 2006-2010 buses with specific wheelchair lifts because roll stop latches may bend, allowing occupants to fall from the elevated platform.

    Product
    STARCRAFT — STARCRAFT STARQUEST, XLT, ULTRASTAR, ALLSTAR XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·12201·2012-06-21

    Flushmate III Pressure-Assist Flushing System Recalled for Bursting Hazards

    Flushmate is recalling approximately 2.3 million Flushmate III pressure-assist flushing systems in the U.S. and Canada because the units can burst, posing impact and laceration hazards.

    Product
    Flushmate® III Pressure-Assist Flushing System
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·12T012000·2012-06-21

    Del-Nat Recalls Tires Due to Potential Tread Separation Risk

    Del-Nat is recalling specific Delta A/S Sierradial and National A/S Commando tires because contaminated rubber may cause tread separation, increasing crash risk.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·12V287000·2012-06-21

    Navistar Recalls IC Bus CE and RE Models for Roof Hatch Defect

    Navistar is recalling 2012-2013 IC Bus CE and RE models because roof escape hatches may be difficult to open in an emergency, potentially hindering egress.

    Product
    IC BUS — IC BUS RE, CE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1391-2012·2012-06-20

    Crispy Cookies Recalled for Undeclared Milk Allergen

    House of Spices (India) Inc. is recalling Crispy Coconut, Almond, and Pistachio Cookies because they may contain undeclared milk.

    Product
    Crispy Coconut Cookies is labeled in part: "***VEGETARIAN***NO EGG***CRISPY***By TWI Foods***COCONUT COOKIES***Just Baked!***Biscuit noix de coco***Manufactured by: ***www.crispyjustbaked.com***TWI FOODS INC***2600 Drew Road, Mississauga, ON Canada L4T 3M5 1-866-9-CRISPY***Ingr
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1406-2012·2012-06-20

    Superior Nut Company Liquid Peanut Butter Topping Recalled for Aflatoxin

    Superior Nut Company is recalling liquid peanut butter topping because aflatoxin levels exceeded the 20 parts per billion limit.

    Product
    Liquid Peanut Butter Topping under the Brand name: Superior Nut Company, Murray's, Dairy Queen packaged in 6.5 lb., 45 lb.
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Drugs)·D-1369-2012·2012-06-20

    Meridian Recalls Diazepam Autoinjectors Due to High Carbostyril Levels

    Meridian Medical Technologies is recalling 83,400 Diazepam autoinjectors because they contain high levels of carbostyril, a known degradation product.

    Product
    DIAZEPAM — DIAZEPAM (DIAZEPAM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1395-2012·2012-06-20

    Better Batter Chocolate Mix Recalled for Undeclared Milk Allergen

    Raymond Hadley Corporation is recalling Better Batter Chocolate Mix because it contains undeclared milk, a known allergen, from a sub-ingredient.

    Product
    better batter brand CHOCOLATE MIX, A GLUTEN FREE BAKING MIX, 18.25 oz (517 g), UPC 8 96439 00209 4. The mix is packaged in a chip board box.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1393-2012·2012-06-20

    Better Batter Gluten Free Pancake Mix Recalled for Undeclared Milk

    Raymond Hadley Corporation is recalling Better Batter Gluten Free Pancake & Biscuit Mix because it contains undeclared milk, a known allergen.

    Product
    better batter brand Gluten Free Pancake & Biscuit Mix packaged in chip board box, in 20 oz. (UPC 8 96439 00207 0) and in 2.5 lb sizes (UPC 8 96439 00203 2). The 20 oz. product is labeled in part, "*** better batter PANCAKE & BISCUIT MIX *** 20 OZ *** UPC 8 96439 00207 0***".
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1397-2012·2012-06-20

    Raymond Hadley Gluten Free White Cake Mix Recalled for Undeclared Milk

    Raymond Hadley Corporation is recalling 29 packages of #1 Gluten Free White Cake Mix because it contains undeclared milk, a known allergen.

    Product
    #1 Gluten Free brand White Cake Mix, 5 lb., UPC 6 54367 43505 2.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1398-2012·2012-06-20

    Taylor Farms Recalls Organic Baby Spinach Due to Salmonella Test

    Taylor Farms Retail, Inc. is recalling specific lots of Private Selections and Marketside Organic Baby Spinach after a USDA sample tested positive for Salmonella.

    Product
    Private Selections Organic Baby Spinach, 5 oz plastic clamshell, UPC 0-11110-91128-5; Marketside Baby Spinach Organic, 10 oz plastic clamshell, UPC: 6-8113132900-2
    Category
    Food
    Distribution
    18 states
  • SevereFDA (Food)·F-1435-2012·2012-06-20

    CTC Food International Recalls Orchids Brand Whole Oysters Due to Insanitary Conditions

    CTC Food International is recalling Orchids brand Whole Oysters because they were prepared or packed under insanitary conditions that may have rendered them injurious to health.

    Product
    Orchids brand Whole Oysters, Net Wt. 8 oz (226 g) Ingredients: oysters, salt, water. Packed for CTC Food Int'l Inc. South San Francisco, CA 94080 Product of Korea
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1390-2012·2012-06-20

    Crispy Cookies Recalled for Undeclared Milk and Almonds

    House of Spices (India) Inc. is recalling Crispy Coconut, Almond, and Pistachio Cookies due to potential undeclared milk and almonds.

    Product
    1) Crispy Pistachio Cookies is labeled in part: "***VEGETARIAN***NO EGG***CRISPY***By TWI Foods***PISTACHIO COOKIES***Just Baked!***Biscuit Pistache***Net Wt./Poids Net 200g/7oz***TWI FOODS INC***1869 Cage Court, Mississauga, ON Canada L5S 1S3. 1-866-9-CRISPY*** ; 2) Crispy Pis
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1419-2012·2012-06-20

    J&I Trading Group Recalls Fresh Baby Clam Meat Due to Sanitation Concerns

    J&I Trading Group, Inc. is recalling 15 cases of Fresh Baby Clam Meat because the shellfish was harvested from waters potentially exposed to inadequate sanitation controls.

    Product
    Fresh Baby Clam Meat Labels on outer styrofoam container; 200 g packages, 30 or 40 packages/case, refrigerated. Refrigerate after opening. Product arrived via Korean Air Cargo directly to consignees.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1371-2012·2012-06-20

    Airgas Recalls Carbon Dioxide Medical Gas Cylinders Due to Impurities

    Airgas Inc is recalling 123 cylinders of Carbon Dioxide, USP, Medical Gas due to out-of-specification levels of nitrogen dioxide. The affected product was distributed to medical facilities in Arizona and California.

    Product
    Carbon Dioxide, USP, Medical Gas, packaged in a) size EA aluminum, CGA940 (CDUSPEA), b) size E CGA 940 (CDUSPE), c) 50 lb CGA320 (CDUSP50, CD USP50S), d) size 160 liter (CD USP160LT350) cylinders, Rx only, Airgas, Puritan Medical, Distributed By: Airgas USA, LLC, Radnor, PA.
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-1370-2012·2012-06-20

    Bausch & Lomb Recalls Murocel Lubricant Ophthalmic Solution Due to Sterility Concerns

    Bausch & Lomb is recalling 59,777 bottles of Murocel Lubricant Ophthalmic Solution because the product failed antimicrobial effectiveness testing.

    Product
    Murocel (methylcellulose) Lubricant Opthalmic Solution (USP, 1%), 15 mL bottle, OTC, Manufactured by Bausch & Lomb Incorporated, Tampa, FL 33637, NDC 24208-280-15
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1394-2012·2012-06-20

    Better Batter Gluten-Free Yellow Cake Mix Recalled for Undeclared Milk

    Raymond Hadley Corporation is recalling Better Batter Yellow Cake Mix because it contains undeclared milk, a known allergen.

    Product
    better batter brand YELLOW CAKE MIX, A GLUTEN FREE BAKING MIX, 18.25 oz. (517 g), UPC 8 96439 00210 0. The mix is packaged in a chip board box.
    Category
    Food
    Distribution
    0 states
  • SevereNHTSA·12V283000·2012-06-20

    Navistar Recalls 2013 International Durastar Trucks for Windshield Defect

    Navistar is recalling 1,298 2013 International Durastar trucks because windshield and backlight glass may separate from the cab, increasing the risk of injury or death.

    Product
    INTERNATIONAL — INTERNATIONAL DURASTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1405-2012·2012-06-20

    Bear Paws Pastry Recalled for Undeclared Wheat Allergen

    JDS Bakery LLC is recalling Bear Paws Microwaveable Pastry because the labels do not declare wheat, a major food allergen.

    Product
    Bear Paws MICROWAVEABLE A Pastry Ingredients: Flour (unbleached), powdered sugar, sugar, walnuts, water, vegetable shortening Net Wt 8oz Stahl's Bakery (586) 716-8500
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1410-2012·2012-06-20

    Kerry Ingredients Recalls Spicy Chicken Marinade Due to Salmonella Risk

    Kerry Ingredients & Flavours is recalling Spicy Chicken Marinade because ingredients used in its manufacture tested positive for Salmonella.

    Product
    Spicy Chicken Marinade, item number 724435.01. Distributed by Kerry Ingredients & Flavours 3330 Millington Road, Beloit, WI 53511 Ingredients: salt, modified corn starch, yeast extract, garlic powder, spice, onion powder, chicken fat, natural flavor, soybean oil, maltodextrin, ci
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1412-2012·2012-06-20

    Kerry Ingredients Recalls Spicy Chicken Marinade Due to Salmonella Risk

    Kerry Ingredients & Flavours is recalling Spicy Chicken Marinade - Bake because ingredients used in its manufacture tested positive for Salmonella.

    Product
    Spicy Chicken Marinade - Bake, item number 724444.01 Distributed by Kerry Ingredients & Flavours 3330 Millington Road, Beloit, WI 53511 Ingredients: salt, yeast extract, modified corn starch, dried chicken broth, onion powder, garlic powder, natural flavor, dried red pepper sauce
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1436-2012·2012-06-20

    Orchids Smoked Oysters Recalled for Potential Contamination

    CTC Food International is recalling Orchids brand Smoked Oysters due to potential contamination from insanitary conditions.

    Product
    Orchids brand Smoked Oysters in cottonseed oil, salt added. Net Wt. 3 oz Ingredients: oysters, salt, water. Packed for CTC Food Int'l Inc. South San Francisco, CA 94080 Product of Korea
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1420-2012·2012-06-20

    Cheese Coffee Cake Recalled for Undeclared Milk Allergen

    Super Mom's is recalling Country Fresh Ovens Cheese Coffee Cake because label audits found an undeclared milk allergen.

    Product
    Country Fresh Ovens Cheese Coffee Cake, Net Wt 5 oz (142g). Dist. by Country Fresh Ovens, St. Paul Park, MN 55071
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1792-2012·2012-06-20

    MicroAire Lipofilter 3000 Canisters Recalled for Sterilization Defects

    MicroAire Surgical Instruments is recalling 15 Lipofilter 3000 fat collection canisters because they were not manufactured under Good Manufacturing Procedures, potentially preventing proper sterilization.

    Product
    Lipofilter 3000, model ASP-CAN-2, labeled in part ***MicroAire, 1641 Edlich Drive, Charlottesville, VA 22911, USA*** Product Usage: A fat collection canister intended for use during liposuction procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1538-2012·2012-06-20

    Philips Healthcare Recalls Mobile X-ray Systems Due to Unintended Radiation

    Philips Healthcare is recalling 11 mobile X-ray systems because they may generate unintended radiation pulses when switched off or parked.

    Product
    Philips Healthcare Practix Convenio Mobile X-ray system Worldwide Distribution -- Nationwide
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·12200·2012-06-20

    Big Lots Recalls Ceramic Space Heaters Due to Fire and Shock Hazards

    Big Lots is recalling about 70,500 portable ceramic space heaters because they can overheat and melt, posing fire and electric shock risks.

    Product
    Portable Space Heater and Portable Oscillating Space Heater
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1810-2012·2012-06-20

    Stryker T4-Hytrel Zipper Toga Recall Due to Missing Tape

    Stryker is recalling T4-Hytrel Zipper Togas because clear tape was not applied during manufacturing, allowing bodily fluids to bleed through the sleeve seam.

    Product
    T4-Hytrel Zipper Toga Product Usage - The togas are intended to provide a barrier between the operating room and the members of the surgical team in order to help protect against contamination and/or exposure of infectious body fluids and harmful microorganisms.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1415-2012·2012-06-20

    Kerry Ingredients Recalls Sliced Beef Gravy Seasoning Due to Salmonella Risk

    Kerry Ingredients & Flavours is recalling Sliced Beef Gravy Seasoning because ingredients used in its manufacture tested positive for Salmonella.

    Product
    Sliced Beef Gravy Seasoning, item number B17806.02 Distributed by Kerry Ingredients & Flavours 3330 Millington Road, Beloit, WI 53511 This product contains milk, soy, wheat (contains sulfiting agents) Ingredients: modified corn starch, hydrolyzed soy protein, autolyzed yeast extr
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1793-2012·2012-06-20

    Aesculap Recalls Columbus Tibia Plateau Components Due to Specification Defects

    Aesculap Implant Systems is recalling eight Columbus Tibia Plateau components because they were found out of specification during internal quality inspection.

    Product
    Columbus Tibia Plateau (component of the Columbus REVISION Knee System) Product Usage - The Columbus Revision Knee System is indicated for use in reconstruction of the diseased knee joint caused by osteoarthritis, rheumatoid arthritis, post-traumatic arthritis, the need to rev
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1788-2012·2012-06-20

    GE Healthcare Revolution XR/d Recalled for Finger Pinch Hazard

    General Electric is recalling 3,796 Revolution XR/d digital radiographic imaging systems worldwide due to a reported incident where an operator's finger was pinched.

    Product
    GE Healthcare Revolution XR/d; GE Healthcare, 3000 North Grandview , Waukesha, WI, 53188 Model numbers: 2259988-2 & 2351505. The Revolution XR/d Digital Radiographic Imaging System is indicated for use in generating radiographic images of human anatomy. It is intended to repl
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1790-2012·2012-06-20

    GE Proteus XR/a Radiographic System Recalled Due to Pinch Hazard

    General Electric is recalling 3,796 Proteus XR/a Radiographic Systems worldwide because an operator's finger was pinched between the fixed roller and the gliding tabletop.

    Product
    GE Proteus XR/a Radiographic System. GE Medical Systems-Americas Milwaukee, WI. Model Number: 2259988. Product is indicated for use in generating radiographic images of human anatomy in all general-purpose diagnostic procedures. This device is not intended for mammographic a
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1399-2012·2012-06-20

    DSM Nutritional Products Recalls Salmonella-Contaminated Roast Meat Flavor

    DSM Nutritional Products, LLC is recalling 13,400 kg of GB Select Roast Meat Type Flavor due to Salmonella contamination. The product was distributed in New Jersey, Wisconsin, and Illinois.

    Product
    GB Select Roast Meat Type Flavor Net Wt. 55 lbs.(25 kg) Product of the Netherlands further processed in China and the US
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1389-2012·2012-06-20

    Best West Foods Recalls Cheese Lasagna Rolls Due to Missing Soy Labeling

    Best West Foods is recalling Cheese Lasagna Rolls because soy was not listed in the ingredient statement or allergen information on the label.

    Product
    Cheese Lasagna Rolls; Perishable, keep frozen; Net weight 15 pounds, 60 x 4 oz. For HRI Use Only. Cook Thoroughly per state food code standards. West Best Foods, inc. 3425 Wynn Road, Las Vegas, NV 89102
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1409-2012·2012-06-20

    Kerry Ingredients Recalls Bourbon Seasoning Due to Salmonella Risk

    Kerry Ingredients & Flavours is recalling Bourbon Seasoning because ingredients used to manufacture it tested positive for Salmonella.

    Product
    Bourbon Seasoning 30458458, item number 30458458.01. Distributed by Kerry Ingredients & Flavours 3330 Millington Road, Beloit, WI 53511 Ingredients: brown sugar, maltodextrin, molasses, yeast extract, spices, dried tomato, worcestershire sauce (distilled vinegar, molasses, corn s
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1789-2012·2012-06-20

    GE Healthcare Definium 8000 Digital Radiographic Systems Recalled for Pinch Hazard

    General Electric is recalling 3,796 Definium 8000 Digital Radiographic Systems because an operator's finger was pinched between the fixed roller and the gliding tabletop.

    Product
    GE Healthcare Definium 8000 Digital Radiographic Systems : GE Healthcare, 3000 North Grandview , Waukesha, WI, 53188 Model Number: 5131070. The Revolution XR/d with Tomosynthesis is intended for use in generating Tomographic images of human anatomy. It is not intended for m
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1809-2012·2012-06-20

    Stryker T5 Hytrel Zipper Toga Recalled for Missing Protective Tape

    Stryker is recalling T5 Hytrel Zipper Togas because clear tape was not applied during manufacturing, allowing bodily fluids to bleed through the sleeve seam.

    Product
    T5 Hytrel Zipper Toga. Product Usage: The togas are intended to provide a barrier between the operating room and the members of the surgical team in order to help protect against contamination and/or exposure of infectious body fluids and harmful microorganisms.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1404-2012·2012-06-20

    JDS Bakery Recalls Cinnamon Rolls Due to Undeclared Wheat Allergen

    JDS Bakery LLC is recalling 60 packages of Cinnamon Rolls A Pastry because the labels fail to declare wheat as an ingredient.

    Product
    Cinnamon Rolls A Pastry Ingredients: Spring Flour (unbleached), water, powdered sugar sugar, vegetable shortening Net Wt 8oz Stahl's Bakery (586) 716-8500
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1392-2012·2012-06-20

    House of Spices Recalls Crispy Cookies for Undeclared Milk

    House of Spices (India) Inc. is recalling Crispy Coconut, Almond, and Pistachio Cookies because they may contain undeclared milk.

    Product
    Crispy Almond Cookie product is labeled in part: "***VEGETARIAN***NO EGG*** CRISPY***By TWI Foods***ALMOND COOKIES***Just Baked!***BISCUIT ALMANDE***Manufactured by***www.crispyjustbaked.com***TWI FOODS INC. 2600 Drew Road, Mississauga, On Canada. L4T 3M5 1-866-9-CRISPY***Ingre
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1396-2012·2012-06-20

    Raymond Hadley Recalls Gluten Free Chocolate Cake Mix for Undeclared Milk

    Raymond Hadley Corporation is recalling 40 packages of #1 Gluten Free brand Chocolate Cake Mix because it contains undeclared milk, a known allergen.

    Product
    #1 Gluten Free brand Chocolate Cake Mix, Net Wt: 5 lb., UPC 6 54367 43530 4
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1414-2012·2012-06-20

    Kerry Ingredients Recalls Thai Seasoning Due to Salmonella Risk

    Kerry Ingredients & Flavours is recalling specific lots of Thai Seasoning because ingredients used in its manufacture tested positive for Salmonella.

    Product
    Thai Seasoning, item number 30502993.01 Distributed by Kerry Ingredients & Flavours 3330 Millington Road, Beloit, WI 53511 Ingredients: sugar, yeast extract, fructose, garlic powder, salt, maltodextrin, corn starch, modified corn starch, spices, dried red bell pepper, citric acid
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1411-2012·2012-06-20

    Kerry Ingredients Recalls Prime Rib Rub Due to Salmonella Risk

    Kerry Ingredients & Flavours is recalling Prime Rib Rub because ingredients used to manufacture it tested positive for Salmonella.

    Product
    Prime Rib Rub, item number B18527.01. Distributed by Kerry Ingredients & Flavours 3330 Millington Road, Beloit, WI 53511 Ingredients: salt, dextrose, yeast extract, malted barley extract, onion powder, garlic powder, spice, maltodextrin, spice extract, and less than 2% silicon d
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1403-2012·2012-06-20

    JDS Bakery Recalls White Brick Oven Bread Due to Undeclared Wheat

    JDS Bakery LLC is recalling 300 packages of White Brick Oven White Bread because the labels fail to declare wheat sub-ingredients.

    Product
    White brick oven WHITE BREAD INGREDIENTS: Spring Flour (unbleached), water vegetable shortning... Stahl's Bakery (586) 716-8500
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1416-2012·2012-06-20

    Kerry Ingredients Recalls Beef Patty Seasoning Due to Salmonella Risk

    Kerry Ingredients & Flavours is recalling Beef Patty Seasoning because ingredients used in its manufacture tested positive for Salmonella.

    Product
    Beef Patty Seasoning, item number B17187.01 Distributed by Kerry Ingredients & Flavours 3330 Millington Road, Beloit, WI 53511 contains soy Ingredients: hydrolyzed soy protein, salt, partially hydrogenated soybean and cottonseed oils, onion powder, dextrose, sugar, tomato powder,
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1413-2012·2012-06-20

    Kerry Ingredients Recalls Italian Marinade Due to Salmonella Risk

    Kerry Ingredients & Flavours is recalling Italian Marinade because ingredients used to manufacture seasonings were found to be positive for Salmonella.

    Product
    Italian Marinade, item number 725450.01 Distributed by Kerry Ingredients & Flavours 3330 Millington Road, Beloit, WI 53511 Ingredients: salt, dried garlic, sugar, corn syrup solids, maltodextrin, yeast extract, spices, dried onion, dried chicken stock, dried red bell pepper, papr
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1490-2012·2012-06-20

    Baxter Sigma Spectrum Infusion Pump Recall for Bearing Failure Risk

    Baxter Healthcare is recalling 63,225 Sigma Spectrum Infusion Pumps because bearing lubricant loss can cause flow failures and potential over-infusion.

    Product
    Sigma Spectrum VOLUMETRIC INFUSION PUMP, with or without Master Drug Library, Part Number 35700 -- Common/Classification Name: Infusion Pump -- Class 2 medical device -- SIGMA LLC, Medina, NY 14103 Product Usage: The Spectrum Infusion Pump is intended to be used for the cont
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1388-2012·2012-06-20

    Best West Foods Recalls Lasagna Rolls Due to Undeclared Soy

    Best West Foods is recalling Cheese and Florentine Lasagna Rolls because soy was not listed on the label. The product was distributed in Nevada.

    Product
    Florentine Lasagna Rolls; Perishable, keep frozen; Net weight 15 pounds, 60 x 4 oz. For HRI Use Only. Cook Thoroughly per state food code standards. West Best Foods, inc. 3425 Wynn Road, Las Vegas, NV 89102
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1421-2012·2012-06-20

    Campbell's Oyster Stew Recalled for Potential Contamination

    Campbell Soup Company is recalling Campbell's Oyster Stew because it may have been prepared under insanitary conditions, posing a potential health risk.

    Product
    Campbell's Oyster Stew, Net Wt 10.5 oz (298g), Campbell Soup Company, Camden, NJ 08103-1701
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1805-2012·2012-06-20

    Vygon Recalls Heparin Lock Flush Syringes and Kits

    Vygon Corporation is recalling Heparin Lock Flush Syringes and kits due to a voluntary recall of related VY Flush Heparin Lock Flush Syringes.

    Product
    Churchill Medical Systems, Inc. VAD ACCESS TRAY Kit Prefilled syringes included in the kit are used to maintain the patency of indwelling catheter lumens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1407-2012·2012-06-20

    Bliss Bros. Dairy Ice Cream Recalled for Aflatoxin Contamination

    Bliss Bros. Dairy is recalling 3-gallon containers of Chocolate Peanut Butter Cookie Dough Ice Cream due to elevated aflatoxin levels in the liquid peanut butter.

    Product
    Bliss Bros. Dairy Chocolate Peanut Butter Cookie Dough Ice Cream, 3-gallon round paperboard,: frozen
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-1430-2012·2012-06-20

    King & Prince Seafood Recalls Mrs. Friday's Breaded Oysters for Insanitary Conditions

    King & Prince Seafood is recalling Mrs. Friday's Gourmet Breaded Oysters because they were prepared under insanitary conditions, posing a potential health risk.

    Product
    Mrs.Friday's brand, Gourmet Breaded Oysters, Small 26-34 CT, Ready to Fry, Net Wt 2.5 lbs (1.13 kg).
    Category
    Food
    Distribution
    13 states
  • ModerateFDA (Devices)·Z-1797-2012·2012-06-20

    Vygon Recalls Heparin Lock Flush Syringes Due to Voluntary Manufacturer Action

    Vygon Corporation is voluntarily recalling specific lots of VY Flush Heparin Lock Flush Syringes and related kits. The recall covers nationwide distribution across 23 states.

    Product
    Vygon VY(TM)Flush Heparin Lock Flush Syringes, 1 Unit per mL, 3mL in a 10mL Flush Syringe, 30 syringes per box Prefilled syringes are used to maintain the patency of indwelling catheter lumens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1794-2012·2012-06-20

    Plasma Surgical Recalls PlasmaJet Open Surgery Handpieces Due to Seal Failure

    Plasma Surgical Inc. is recalling 36 PlasmaJet Open Surgery Handpieces because a potential seal failure may cause a small drop of distilled water coolant to leak during use.

    Product
    PlasmaJet Open Surgery Handpiece (Part of the PlasmaJet Neutral Plasma Surgery System) The PlasmaJet system is a neutral plasma surgery system that is designed for cutting and coagulation in open surgery and laparoscopic surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1798-2012·2012-06-20

    Vygon Recalls Heparin Lock Flush Syringes Due to Voluntary Manufacturer Action

    Vygon Corporation is voluntarily recalling multiple lots of VY Flush Heparin Lock Flush Syringes and related kits. The syringes are used to maintain the patency of indwelling catheter lumens.

    Product
    Vygon VY(TM)Flush Heparin Lock Flush Syringes, 10 Units per mL, 3mL in a 10mL Flush Syringe, 30 syringes per box, Rx only Prefilled syringes are used to maintain the patency of indwelling catheter lumens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1800-2012·2012-06-20

    Vygon Recalls Heparin Lock Flush Syringes Due to Voluntary Manufacturer Action

    Vygon Corporation is voluntarily recalling specific lots of VY Flush Heparin Lock Flush Syringes. The recall covers syringes and kits distributed nationwide.

    Product
    Vygon VY(TM)Flush Heparin Lock Flush Syringes, 100 Units per mL, 3mL in a 10mL Flush Syringe, 30 syringes per box, Rx only Prefilled syringes are used to maintain the patency of indwelling catheter lumens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1377-2012·2012-06-20

    Ben Venue Recalls Octreotide Acetate Injection Due to Potential Low Fill Volume

    Ben Venue Laboratories is recalling Octreotide Acetate Injection vials because some may have low fill volume. The recall covers 6,515 packs distributed nationwide and in Puerto Rico.

    Product
    Octreotide Acetate Injection, 50 mcg/mL (0.05 mg/mL), 1 mL single dose vials, packaged in 10 x 1 mL single dose vials per pack, Rx only, Manufactured for: Bedford Laboratories, Bedford, OH 44146; Manufactured by: Ben Venue Laboratories, Inc., Bedford, OH 44146; NDC 55390-160-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1401-2012·2012-06-20

    Panera Cream Cheese Spread Recalled for Ingredient Labeling Error

    Panera Bread LLC is recalling Reduced Fat Hazelnut Cream Cheese Spread because the ingredient statement on the label was reversed. The product name on the label is correct.

    Product
    Panera ,HAZELNUT CREAM CHEESE SPREAD Reduced Fat, 8 0z , Refrigerated
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1422-2012·2012-06-20

    Polar Whole Boiled Oysters Recalled for Insanitary Conditions

    Milky Way Intl Trading Corp is recalling Polar Whole Boiled Oysters due to insanitary conditions that may have contaminated the product.

    Product
    Polar Whole Boiled Oysters, 8 oz. net weight, 12 cans/carton.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1808-2012·2012-06-20

    Vygon Recalls Heparin Lock Flush Syringes and PICC Insertion Kits

    Vygon is recalling Heparin Lock Flush Syringes and kits containing them due to a voluntary recall of similar syringes by the manufacturer.

    Product
    Churchill Medical Systems, Inc. A VYGON COMPANY PICC INSERTION TRAY Prefilled syringes included in the kit are used to maintain the patency of indwelling catheter lumens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1378-2012·2012-06-20

    Luitpold Recalls Concentrated Sodium Chloride Injection Due to Particulate Matter

    Luitpold Pharmaceuticals is recalling concentrated sodium chloride injection vials because visual particles were found in retention samples.

    Product
    CONCENTRATED SODIUM CHLORIDE INJECTION, USP, 23.4% a) 30 mL SINGLE DOSE VIAL, (NDC 0517-2930-25), b) 100 mL PHARMACY BULK PACKAGE (NDC 0517-2900-25), Rx Only, AMERICAN REGENT, INC. SHIRLEY, NY 11967.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1425-2012·2012-06-20

    Crown Prince Canned Oysters Recalled for Insanitary Conditions

    Crown Prince Inc is recalling 8 oz cans of Whole Boiled Oysters because they were prepared under insanitary conditions, posing a potential health risk.

    Product
    Canned oysters. Crown Prince Whole Boiled Oysters, 8 oz. Each case is 8oz/12.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1428-2012·2012-06-20

    Crown Prince Canned Smoked Oysters Recalled for Insanitary Conditions

    Crown Prince Inc is recalling canned smoked oysters prepared under insanitary conditions that may have rendered them injurious to health.

    Product
    Canned oysters. Crown Prince Natural Smoked Oysters with Chili Pepper, 3 oz. Each case is 3oz/18.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1379-2012·2012-06-20

    Physicians Total Care Recalls Arthrotec 75 Tablets Due to Broken Tablets

    Physicians Total Care is recalling specific lots of Arthrotec 75 tablets because they may contain broken tablets. The recall affects products distributed in North Carolina and Kentucky.

    Product
    Arthrotec 75 (diclofenac sodium and misoprostol) tablets, 75 mg/200 mcg, a) 30-count tablets per bottle (NDC 54868-4165-1); b) 60-count tablets per bottle (NDC 54868-4165-0); Rx only, Mfg. By: G.D. searle LLC Div Pfizer, New York, NY 10017; Repacked & distributed by: Physicians
    Category
    Drug
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1806-2012·2012-06-20

    Vygon Recalls Heparin Lock Flush Syringes and Kits

    Vygon is voluntarily recalling Heparin Lock Flush Syringes and kits containing them due to a related recall of VY Flush Heparin Lock Flush Syringes.

    Product
    Churchill Medical Systems, Inc. VAD ACCESS TRAY Kit Prefilled syringes included in the kit are used to maintain the patency of indwelling catheter lumens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1807-2012·2012-06-20

    Vygon Recalls Heparin Lock Flush Syringes and Dressing Change Kits

    Vygon Corporation is voluntarily recalling Heparin Lock Flush Syringes and kits containing them due to a related recall of VY Flush Heparin Lock Flush Syringes.

    Product
    Churchill Medical Systems, Inc. DRESSING CHANGE KIT Prefilled syringes included in the kit are used to maintain the patency of indwelling catheter lumens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1799-2012·2012-06-20

    Vygon Recalls Heparin Lock Flush Syringes Due to Voluntary Manufacturer Action

    Vygon Corporation is voluntarily recalling multiple lots of VY Flush Heparin Lock Flush Syringes and related kits. The recall covers products distributed nationwide.

    Product
    Vygon VY(TM)Flush Heparin Lock Flush Syringes, 10 Units per mL, 5mL in a 10mL Flush Syringe, 30 syringes per box, Rx only Prefilled syringes are used to maintain the patency of indwelling catheter lumens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1433-2012·2012-06-20

    Chicken of the Sea Recalls Oysters Due to Insanitary Conditions

    Chicken of the Sea is recalling specific oyster products because they were prepared or packed under insanitary conditions that may have rendered them injurious to health.

    Product
    1) Chicken of the Sea Whole Oysters Pieces 24 units per case, UPC 4800000069; 2) Pacific Pearl Whole Oysters Pieces 12 units per case, UPC 7175902112
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1417-2012·2012-06-20

    Napoleon Canned Smoked Oysters Recalled for Insanitary Conditions

    The Napoleon Company is recalling canned smoked oysters prepared under insanitary conditions that may have rendered the product injurious to health.

    Product
    Napoleon canned, Smoked Oysters, Medium. Item no. 48-312. Net WT. per can is 3.66 oz (106 g). The UPC is 0 41253 00312 7. The product is labeled in parts: "***NAPOLEON***Medium***SMOKED OYSTERS***NET WT. 3.66 OZ (106 g)***INGREDIENTS: SMOKED OYSTERS, SOYA OIL, SALT***PRODUC
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-1402-2012·2012-06-20

    Stahl's Famous Original Bakery Cutout Cookies Recalled for Undeclared Ingredients

    JDS Bakery LLC is recalling 80 packages of 14-oz Stahl's Famous Original Bakery Cutout Cookies because the labels fail to declare specific sub-ingredients.

    Product
    Stahl's Famous Original Bakery CUTOUT COOKIES 14oz. INGREDIENTS: Pastry Flour, Sugar, Shortening...Contains Wheat, Eggs, Milk and Soy.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-1376-2012·2012-06-20

    Ben Venue Recalls Midazolam HCl Injection Due to Potential Low Fill Volume

    Ben Venue Laboratories is recalling Midazolam HCl Injection vials because some may have low fill volume. The recall covers 11,161 packs distributed nationwide and in Puerto Rico.

    Product
    Midazolam HCl Injection, 5 mg/mL, 1 mL single use vials, packaged in 10 x 1 mL single use vials per pack, Rx only, Manufactured by: Ben Venue Laboratories, Inc., Bedford, OH 44146; Manufactured for: Bedford Laboratories, Bedford, OH 44146, NDC 55390-138-01; UPC 3 55390-138-01 8
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1804-2012·2012-06-20

    Vygon Recalls Heparin Lock Flush Syringes and PICC Insertion Kits

    Vygon is recalling heparin lock flush syringes and kits containing them due to a voluntary recall of VY Flush Heparin Lock Flush Syringes.

    Product
    Churchill Medical Systems, Inc. A VYGON Company PICC INSERTION TRAY Kit Prefilled syringes included in the kit are used to maintain the patency of indwelling catheter lumens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1381-2012·2012-06-20

    Endo Pharmaceuticals Recalls Endocet Tablets Due to Foreign Tablet Contamination

    Endo Pharmaceuticals is recalling specific bottles of Endocet 10 mg/650 mg tablets because some contained mixed 10 mg/325 mg tablets.

    Product
    Endocet (oxycodone and acetaminophen) tablets, USP, 10 mg/650 mg, 100-count tablets per bottle, Rx only, Manufactured for: Endo Pharmaceuticals Inc., Chadds Ford, PA, By: Novartis, Lincoln, NE 68501; NDC 60951-797-70.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1374-2012·2012-06-20

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Pharmaceuticals is recalling 244,320 Daytrana patches because the delivery system is miscalibrated or defective, making it difficult to remove the release liner.

    Product
    Daytrana (methylphenidate) transdermal system patch, Delivers 15 mg over 9 hours (1.6 mg/hr), 1 patch per pouch (NDC 54092-553-01), packaged in 30-count patches per box (NDC 54092-553-30), Rx only, Manufactured for Shire US Inc., Wayne, PA 19087; by Noven Pharmaceuticals, Inc.,
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1372-2012·2012-06-20

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Pharmaceuticals is recalling 357,510 Daytrana (methylphenidate) patches because the delivery system may be miscalibrated or defective, affecting the ability to remove the release liner.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1375-2012·2012-06-20

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Pharmaceuticals is recalling 335,190 Daytrana patches because the delivery system may be miscalibrated or defective, affecting the ability to remove the release liner.

    Product
    Daytrana (methylphenidate) transdermal system patch, Delivers 10 mg over 9 hours (1.1 mg/hr), 1 patch per pouch (NDC 54092-552-01), packaged in 30-count patches per box (NDC 54092-552-30), Rx only, Manufactured for Shire US Inc., Wayne, PA 19087; by Noven Pharmaceuticals, Inc.,
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1803-2012·2012-06-20

    Vygon Recalls Heparin Lock Flush Syringes and Kits

    Vygon Corporation is voluntarily recalling Heparin Lock Flush Syringes and kits containing them due to a related recall of VY Flush Heparin Lock Flush Syringes.

    Product
    Churchill Medical Systems, Inc. PORT-A-CATH Tray Kit Prefilled syringes included in the kit are used to maintain the patency of indwelling catheter lumens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1801-2012·2012-06-20

    Vygon Recalls Heparin Lock Flush Syringes Due to Voluntary Manufacturer Action

    Vygon Corporation is voluntarily recalling multiple lots of VY Flush Heparin Lock Flush Syringes and related kits nationwide.

    Product
    Vygon VY(TM)Flush Heparin Lock Flush Syringes, 100 Units per mL, 5mL in a 10mL Flush Syringe, 30 syringes per box, Rx only Prefilled syringes are used to maintain the patency of indwelling catheter lumens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1802-2012·2012-06-20

    Vygon Recalls Heparin Lock Flush Syringes and Kits

    Vygon is recalling heparin lock flush syringes and kits due to a manufacturer recall of VY Flush Heparin Lock Flush Syringes.

    Product
    Churchill Medical Systems, Inc. A VYGON Company PICC LINE TRAY Kit Prefilled syringes included in the tray kit are used to maintain the patency of indwelling catheter lumens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1791-2012·2012-06-20

    Philips Brilliance iCT and iCT SP CT Systems Software Update Recall

    Philips is issuing a software update for Brilliance iCT and iCT SP systems to address non-conformances that do not result in unacceptable hazards.

    Product
    The Brilliance iCT and iCT SP are Computed Tomography X-Ray Systems intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes. These devices may include signal analysis and display equipment,
    Category
    Medical Device
    Distribution
    22 states
  • ModerateFDA (Food)·F-1424-2012·2012-06-20

    Daufuski Brand Boiled Oysters Recalled for Insanitary Conditions

    Liberty Gold Fruit Company is recalling Daufuski Brand boiled oysters due to preparation under insanitary conditions that may have contaminated the product.

    Product
    Daufuski Brand boiled Oysters, 8 oz; Distributed by Liberty Gold Fruit, Inc.
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Drugs)·D-1373-2012·2012-06-20

    Daytrana Transdermal Patch Recalled for Defective Delivery System

    Noven Pharmaceuticals is recalling Daytrana transdermal patches because the release liner may be difficult to remove. This could affect the patient's ability to apply the medication correctly.

    Product
    Daytrana (methylphenidate) transdermal system patch, Delivers 30 mg over 9 hours (3.3 mg/hr), 1 patch per pouch (NDC 54092-555-01), packaged in 30-count patches per box (NDC 54092-555-30), Rx only, Manufactured for Shire US Inc., Wayne, PA 19087 by Noven Pharmaceuticals, Inc., Mi
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1408-2012·2012-06-20

    Newport Creamery Chocolate Peanut Butter Frozen Yogurt Recalled for Aflatoxin

    Bliss Bros Dairy is recalling Newport Creamery Chocolate Peanut Butter Frozen Yogurt due to elevated aflatoxin levels in the liquid peanut butter ingredient.

    Product
    Newport Creamery Chocolate Peanut Butter Frozen Yogurt 3-gallon containers and 80 half gallon containers
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-1432-2012·2012-06-20

    Chicken of the Sea Recalls Oysters Due to Insanitary Conditions

    Chicken of the Sea is recalling specific oyster products because they were prepared or packed under insanitary conditions, posing a potential health risk.

    Product
    1) Chicken of the Sea Whole Oysters, 12 units per case, 8oz., UPC 4800000267; 2) Ace of Diamonds Whole Oysters 24 units per case, UPC 7760015508
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1434-2012·2012-06-20

    Chicken of the Sea Recalls Smoked Oyster Water for Sanitation Issues

    Chicken of the Sea is recalling Pacific Pearl Smoked Oyster Water because the product was prepared under insanitary conditions that may have caused contamination.

    Product
    Pacific Pearl Smoked Oyster Water 12 units per case
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1429-2012·2012-06-20

    King & Prince Seafood Recalls Breaded Oysters for Insanitary Conditions

    King & Prince Seafood is recalling Mrs. Friday's Gourmet Breaded Oysters because they were prepared or packed under insanitary conditions, posing a potential health risk.

    Product
    1) Mrs.Friday's brand, Gourmet Breaded Oysters, Medium 18-25 CT, Ready to Fry, Net Wt 2.5 lbs (1.13 kg). 2) Mrs.Friday's brand, (Canada) Gourmet Breaded Oysters, Medium, Ready to Fry, Net Wt 2.5 lbs (1.13 kg), Distributed by King & Prince Corp., Brunswick, GA 31521. Product is p
    Category
    Food
    Distribution
    13 states
  • ModerateFDA (Food)·F-1418-2012·2012-06-20

    Napoleon Canned Smoked Oysters Recalled for Insanitary Conditions

    The Napoleon Company is recalling canned smoked oysters prepared under insanitary conditions that may have contaminated the product.

    Product
    Napoleon canned, Smoked Oysters, Large. Item no. 48-313. Net WT. per can is 3.66 oz (106 g). The UPC is 0 41253 00313 4. The product is labeled in parts: "***NAPOLEON***Large***SMOKED OYSTERS***NET WT. 3.66 OZ (106 g)***INGREDIENTS: SMOKED OYSTERS, SOYA OIL, SALT***PRODUCT
    Category
    Food
    Distribution
    3 states

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