The Recall Desk

Archive

March 2013 recalls

461 recalls were announced in March 2013.

What the numbers show

Critical
39
Severe
148
High
159
Moderate
84
Low
31

Of the 461 recalls this month scored against our rubric, 8% are Critical, 32% are Severe.

Which agencies issued them

201–300 of 461

  • HighFDA (Food)·F-1119-2013·2013-03-20

    Dakota Specialty Milling Recalls Organic Wheat Flour Due to Metal Wire Fragments

    Dakota Specialty Milling is recalling organic wheat flour and blends due to potential contamination with pliable metal wire mesh fragments from a defective sifter.

    Product
    4060801, ORGANIC HIGH GLUTEN REFINED HARD RED SPRING WHEAT FLOUR(ORGANIC WHEAT), DAKOTA SPECIALTY MILLING, INC., FARGO, ND , 1 NET WT 50 LBS..
    Category
    Food
    Distribution
    21 states
  • HighFDA (Devices)·Z-0946-2013·2013-03-20

    Natus Neurology Recalls Nicolet EEG Wireless Amplifiers Due to Overheating Risk

    Natus Neurology is recalling 114 Nicolet EEG Wireless Amplifiers because they may overheat near the on/off button, posing a risk of discomfort or burns.

    Product
    Nicolet EEG Wireless Amplifier 32/64 Channel. Catalog/Part Numbers : 515-015400 for the 32 channel amplifier and 515-015500 for the 64 channel amplifier. Product Usage: The Nicolet Wireless EEG Amplifier is intended to be used as a front end amplifier to acquire, store, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1098-2013·2013-03-20

    Dakota Specialty Milling Recalls Whole Grain Blend Flour Due to Metal Wire Fragments

    Dakota Specialty Milling is recalling specific lots of 12 Whole Grain Blend flour because they may contain pliable metal wire mesh fragments from a defective sifter.

    Product
    41512 and 41512-T, IBC 12 WHOLE GRAIN BLEND( WHEAT, OATS, BARLEY , RYE, TRITICALE, MILLET, BUCKWHEAT, YELLOW CORN, SORGHUM, BROWN RICE, QUINOA, AMARANTH) DAKOTA SPECIALTY MILLING, INC., FARGO, ND , 1 NET WT. 50. LBS and 1,750 LBS.
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-1103-2013·2013-03-20

    Dakota Specialty Milling Recalls 9 Grain Blend Flour Due to Metal Wire Mesh

    Dakota Specialty Milling is recalling Nickles 9 Grain Blend flour because it may contain pliable metal wire mesh fragments from a defective sifter.

    Product
    41681, NICKLES 9 GRAIN BLEND ( OATS, WHEAT, BARLEY, TRITICALE, WHITE WHEAT, BROWN FLAX, RYE, AMARANT, WHEAT GERM, CORN, BROWN RICE), DAKOTA SPECIALTY MILLING, INC., FARGO, ND , 1 NET WT. 50 LBS .
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-1199-2013·2013-03-20

    Mandalay Trading Recalls Tausi Brand Salted Black Beans

    Mandalay Trading is recalling Tausi Brand Salted Black Beans due to potential pathogen growth and toxin formation from Clostridium botulinum or other spoilage organisms.

    Product
    Tausi Brand Salted Black Beans, 180g (6.34oz), 100 cans/carton This product is in a two piece can with a single seam. This 6.34 oz can is wrapped with a label containing, red, yellow, and black text labeled in part "Tausi Brand Salted Black Beans***Distributed by: V8 Commercial…
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0949-2013·2013-03-20

    Hill-Rom TotalCare SpO2RT2 Bed Recalled for Software Pressure Issue

    Hill-Rom is recalling 309 TotalCare SpO2RT2 beds due to a software defect that may reduce surface cushion pressure, potentially increasing the risk of skin irritation for high-risk patients.

    Product
    TotalCare SpO2RT2 bed. Product Usage: Bed, flotation therapy, powered bed may be used in a variety of settings including, but not limited to, acute care, including critical care, step down/progressive care, medical/surgical, high acuity sub-acute care, post anesthesia…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1101-2013·2013-03-20

    Dakota Specialty Milling Recalls Flour Blends Due to Metal Wire Fragments

    Dakota Specialty Milling is recalling flour and flour blends that may contain pliable metal wire mesh fragments from a defective sifter.

    Product
    41672, SPECIALTY LIGHT WHITE BLEND 200 ( CELLULOSE FIBER, WHEAT FLOUR, SALT, CELLULOSE GUM, GUAR GUM, CALCIUM PROPIONATE), DAKOTA SPECIALTY MILLING, INC., FARGO, ND , 19 NET WT. 50 LBS .
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-1100-2013·2013-03-20

    Dakota Specialty Milling Recalls 8-Grain Flour Blend for Metal Wire Fragments

    Dakota Specialty Milling is recalling 8-Grain Instantized flour blends due to potential contamination with pliable metal wire mesh fragments from a defective sifter.

    Product
    41653, MIX 8 GRAIN INSTANTIZED( OATS, WHEAT, BARLEY, TRITICALE, WHITE WHEAT, RYE, AMARANTH, FLAXSEED, WHEAT GERM, YELLOW CORN), DAKOTA SPECIALTY MILLING, INC., FARGO, ND , 1 NET WT. 50 LBS .
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-1105-2013·2013-03-20

    Dakota Specialty Milling Recalls Flour Blends Due to Metal Wire Mesh Fragments

    Dakota Specialty Milling is recalling specific flour and flour blends because they may contain pliable metal wire mesh fragments from a defective sifter.

    Product
    42203, OCTOBER GRAINS & SEEDS MIX ( OATS, GOLDEN FLAX, SUNFLOWER, SESAME SEED, WHITE WHEAT, OAT FLOUR, BARLEY, WHET BRAN, CORN, MILLET, AMARANTH), DAKOTA SPECIALTY MILLING, INC., FARGO, ND , 1 NET WT. 50 LBS .
    Category
    Food
    Distribution
    21 states
  • HighFDA (Devices)·Z-0920-2013·2013-03-20

    Integra CUSA CEM Nosecone Recalled for Potential Tip Erosion

    Integra LifeSciences is recalling CEM Nosecones for the CUSA EXcel system due to a potential for tip erosion and breakage. No patient injuries have been reported.

    Product
    Integra CUSA excel. CEM Nosecone for CUSA EXcel System. The CEM Nosecone is intended for use CUSA Excel/CUSA Excel + Ultrasonic Surgical Aspiration System, CUSA handpiece, and Covidien Force FX Electrosurgical Generator. Used in surgical procedures where combined…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1142-2013·2013-03-20

    Food For Life Recalls Ezekiel 4:9 Cereal for Undeclared Almond

    Food For Life Baking Company is recalling Ezekiel 4:9 Sprouted Grain Cereal because it may contain undeclared almonds, a major allergen.

    Product
    Ezekiel 4:9 Sprouted Grain Cereal- Golden Flax, 16 oz. Packaging label reads in part:" Food FOR Life***EZEKIEL 4:9 SPROUTED WHOLE GRAIN CEREAL GOLDEN FLAX***NET WT. 16 OZ(454g)***MANUFACTURED BY: FOOD FOR LIFE BAKING COMPANY, INC. P.O. BOX 1434 CORONA, CA 92878-1434***".
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1189-2013·2013-03-20

    Bay Valley Foods Recalls Pasta Mix for Missing Soy Labeling

    Bay Valley Foods is voluntarily recalling boxed pasta mix products because the ingredient labels failed to list soy lecithin.

    Product
    55613210946 Western Family, Easy Sides, Herb & Butter Pene, Net WT 5.5 oz (156 g), UPC "0 15400 12655 7", Proudly Distributed by Western Family Foods, Inc., P.O. Box 4057, Portland OR, 97208
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-1088-2013·2013-03-20

    Dakota Specialty Milling Recalls 9 Grain Blend Due to Metal Wire Fragments

    Dakota Specialty Milling is recalling Specialty 9 Grain Blend 400 because it may contain pliable metal wire mesh fragments from a defective sifter.

    Product
    40180, SPECIALTY 9 GRAIN BLEND 400 ( OATS, WHITE WHEAT, BARLEY, RYE, TRITICALE, SPELT, BUCKWHEAT, MILLET, BROWN RICE), DAKOTA SPECIALTY MILLING, INC., FARGO, ND , 1 Net WT 50 LBS.
    Category
    Food
    Distribution
    21 states
  • HighFDA (Devices)·Z-0926-2013·2013-03-20

    Medtronic O-arm Imaging System Recalled for Braking System Failure

    Medtronic is recalling 463 O-arm Imaging Systems worldwide due to a potential failure of the braking system controlling vertical gantry movement.

    Product
    Medtronic O-arm Imaging System Product Usage: image-intensified fluoroscopic x-ray system, mobile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1091-2013·2013-03-20

    Dakota Specialty Milling Recalls 12 Grain Blend Due to Metal Wire Fragments

    Dakota Specialty Milling is recalling its 12 Grain Blend because it may contain pliable metal wire mesh fragments from a defective sifter.

    Product
    40730, SPECIALTY DAKOTA 12 GRAIN BLEND 200( WHEAT, OATS , BARLEY, RYE, TRICALE, MILLET, BROWN RICE, BULGUR WHEAT, YELLOW CORN, BUCKWHEAT, SPELT, AMARANTH), DAKOTA SPECIALTY MILLING, INC., FARGO, ND , 1 Net WT 50 LBS.
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-1102-2013·2013-03-20

    Dakota Specialty Milling Recalls 12 Grain Blend Due to Metal Wire Fragments

    Dakota Specialty Milling is recalling Nickles 12 Grain Blend because it may contain pliable metal wire mesh fragments from a defective sifter.

    Product
    41678, NICKLES 12 GRAIN BLEND ( SUNFLOWER, WHEAT, OATS, WHOLE WHEAT FLOUR, SESAME SEEDS, FLAXSEED, BARLEY, RYE, TRICALE, BROWN RICE, MILLET, YELLOW CORN, BUCKWHEAT, BULGUR WHEAT, AMARANTH, QUINOA), DAKOTA SPECIALTY MILLING, INC., FARGO, ND , 1 NET WT. 50 LBS .
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-1092-2013·2013-03-20

    Dakota Specialty Milling Recalls 11 Grain Blend Due to Metal Wire Fragments

    Dakota Specialty Milling is recalling its Specialty 11 Grain Blend because it may contain pliable metal wire mesh fragments from a defective flour sifter.

    Product
    40740, SPECIALTY 11 GRAIN BLEND ( WHEAT,RYE, TRICALE, CORN, BROWN RICE, OATS, BUCKWHEAT, PARLEY, AMARANTH, MILO, QUINOA), DAKOTA SPECIALTY MILLING, INC., FARGO, ND , 1 Net WT 50 LBS.
    Category
    Food
    Distribution
    21 states
  • HighFDA (Devices)·Z-0921-2013·2013-03-20

    Genesys Orthopedic Recalls 3.75mm Fixed Cervical Screws Due to Manufacturing Residue

    Genesys Orthopedic Systems is recalling 3.75mm x 12mm Fixed Cervical Screws because manufacturing residue may be present. The residue poses risks of infection, delayed fusion, or revision surgery.

    Product
    3.75mm x 12mm Fixed Cervical Screws. Components of the Genesys Spine Anterior Cervical Plate System Product Usage: is intended for anterior screw fixation to the cervical spine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1084-2013·2013-03-20

    Dakota Specialty Milling Recalls Flour Blends Due to Metal Wire Mesh Fragments

    Dakota Specialty Milling is recalling flour and flour blends that may contain pliable metal wire mesh fragments from a defective sifter.

    Product
    40133, SARA LEE SPECIALTY 8 GRAIN BLEND 100 (SUNFLOWER, WHEAT, OATS, RYE, BARLEY, WHOLE MEAL YELLOW CORN, MILLET, TRITICALE, RYE FLOUR), DAKOTA SPECIALTY MILLING, INC., FARGO, ND , 1 Net WT 50 LBS.
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-1124-2013·2013-03-20

    Dakota Specialty Milling Recalls 12 Grain Blend Due to Metal Wire Mesh Fragments

    Dakota Specialty Milling is recalling 12 Grain Blend products because they may contain pliable metal wire mesh fragments from a defective sifter.

    Product
    40735, SPECIALTY DAKOTA 12 GRAIN BLEND 100 (WHEAT, OATS, BARLEY, RYE, TRICALE, MILLET, BROWN RICE, BULGAR WHEAT, YELLOW CORN, BUCKWHEAT, SPELT, AMARANTH) DAKOTA SPECIALTY MILLING, INC., FARGO, ND NET WT 50 LBS..
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-1069-2013·2013-03-20

    Nabisco belVita Breakfast Biscuits Recalled for Metal Fragments

    Mondelez Global LLC is voluntarily recalling belVita Breakfast Biscuits due to possible flexible metal mesh fragments from a faulty screen at a flour supplier.

    Product
    Carton: Nabisco belVita Apple Cinnamon Net Wt. 8.8 oz UPC 0 44000 02824 1 Distributed by Kraft Foods Global, Inc. Northfield, IL 60093-2753 USA Inner Pouch: Nabisco belVita Apple Cinnamon Net Wt. 1.76 oz UPC 0 44000 02825 1 Distributed by Kraft Foods Global, Inc.…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0947-2013·2013-03-20

    GE Healthcare Recalls Cardiovascular X-ray Systems Due to Locking Nut Issue

    GE Healthcare is recalling specific cardiovascular X-ray imaging systems because a locking nut on the overhead video monitor suspension might loosen.

    Product
    GE Healthcare Advantx, Innova2000, Innova3100, Innova4100, Innova2100IQ, Innova3100IQ, and Innova4100IQ equipped with Video Monitor Suspension Cardiovascular X-ray imaging systems. Model numbers 2236709, 2353620 ,2223039-2, and 2270677-2.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1081-2013·2013-03-20

    Roman Meal Twelve Grain Flour Recalled for Metal Wire Fragments

    Dakota Specialty Milling is recalling Roman Meal Twelve Grain flour due to potential contamination with pliable metal wire mesh fragments from a defective sifter.

    Product
    13006, Roman Meal Twelve Grain(wheat bran, sunflower seed, stabilized wheat germ, wheat, barley, sesame seed, Millet, yellow corn, flaxseed, Triticale, Oats, Rye, rice flour, black malt, buckwheat flour, spelt, kamut flour, amaranth flour), Roman Meal Company, Tacoma…
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-1143-2013·2013-03-20

    Food For Life Recalls Ezekiel 4:9 Cereal for Undeclared Almond Allergen

    Food For Life Baking Company is recalling specific lots of Ezekiel 4:9 Sprouted Grain Cereal because the product may contain undeclared almonds.

    Product
    Ezekiel 4:9 Sprouted Grain Cereal- Cinnamon Raisin, 16 oz. Packaging label reads in part:" Food FOR Life***EZEKIEL 4:9 SPROUTED WHOLE GRAIN CEREAL Cinnamon Raison***NET WT. 16 OZ(454g)***MANUFACTURED BY: FOOD FOR LIFE BAKING COMPANY, INC. P.O. BOX 1434 CORONA, CA…
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1115-2013·2013-03-20

    Dakota Specialty Milling Recalls Flour Due to Metal Wire Mesh Fragments

    Dakota Specialty Milling is recalling specialty pastry flour and blends due to potential contamination with pliable metal wire mesh fragments from a defective sifter.

    Product
    4060610, SPECIALTY PASTRY FLOUR (SOFT WHITE WHOLE WHEAT), DAKOTA SPECIALTY MILLING, INC., FARGO, ND , 1 NET WT 50 LBS..
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-1109-2013·2013-03-20

    Dakota Specialty Milling Recalls Flour Blends Due to Metal Wire Mesh Fragments

    Dakota Specialty Milling is recalling specific flour and flour blends, including Quadruple Wheat Blend, due to potential contamination with pliable metal wire mesh fragments from a defective sifter.

    Product
    42209, QUADRUPLE WHEAT BLEND( WHITE WHEAT, SPELT, BUCKWHEAT, CALCIUM SULFATE, FERROUS SULFATE-CONTAINS WHEAT STARCH), DAKOTA SPECIALTY MILLING, INC., FARGO, ND , 1 NET WT. 50 LBS .
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-1122-2013·2013-03-20

    Dakota Specialty Milling Recalls Rye Flour Due to Metal Wire Mesh Fragments

    Dakota Specialty Milling is recalling specific lots of medium rye flour because they may contain pliable metal wire mesh fragments from a defective sifter.

    Product
    4060567, MEDIUM RYE FLOUR (RYE), DAKOTA SPECIALTY MILLING, INC., FARGO, ND NET WT 50 LBS..
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-1132-2013·2013-03-20

    Walong Recalls Tausi Brand Salted Black Beans Due to Botulism Risk

    Walong Marketing, Inc. is recalling Tausi Brand Salted Black Beans because the product may support the growth of Clostridium botulinum or other spoilage organisms, posing a risk of toxin formation.

    Product
    Tausi Brand Salted Black Beans, 180g (6.34oz), 100 cans/carton This product is in a two piece can with a single seam. This 6.34 oz can is wrapped with a label containing, red, yellow, and black text labeled in part "Tausi Brand Salted Black Beans***Distributed by: V8 Commercial…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1089-2013·2013-03-20

    North Dakota Multi 7 Grain Bread Mix Recalled for Metal Wire Fragments

    Dakota Specialty Milling is recalling North Dakota Multi 7 Grain Bread Mix due to potential contamination with pliable metal wire mesh fragments from a defective sifter.

    Product
    40450, NORTH DAKOTA MULTI 7 GRAIN BREAD MIX( WHEAT FLOUR, MALTED BARLEY FLOUR, NIACIN, IRON..., RIBOFLAVIN,FOLIC ACID, SUGAR ASCORBIC ACID, NUTRI SOY FLOUR, WHEAT..., BARLEY FLOUR, RYE FLOUR, FLAX MEAL....., OAT BRAN, ROLLED OATS, NONFAT DRY MILK, DRY YEAST), DAKOTA SPECIALTY…
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-1116-2013·2013-03-20

    Dakota Specialty Milling Recalls Barley Flour Due to Metal Wire Fragments

    Dakota Specialty Milling is recalling specific lots of whole meal barley flour because they may contain pliable metal wire mesh fragments from a defective sifter.

    Product
    4060625, WHOLE MEAL BARLEY FLOUR (BARLEY), DAKOTA SPECIALTY MILLING, INC., FARGO, ND , 0 NET WT 50 LBS..
    Category
    Food
    Distribution
    21 states
  • HighFDA (Devices)·Z-0930-2013·2013-03-20

    Siemens ACUSON S2000 ABVS Scanner Recalled for Sharp Transducer Edges

    Siemens is recalling 214 ACUSON S2000 ABVS systems because the transducer pod may contain sharp edges that could cause injury.

    Product
    ACUSON S2000 Automated Breast Volume Scanner (ABVS); Model number 10042541 Distributed by Siemens Medical Solutions USA Inc. business Unit: Ultrasound. The S2000 Automated Breast Volume Scanner (ABVS) Ultrasound System for imaging of the breast allows volumetric…
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Food)·F-1086-2013·2013-03-20

    Dakota Specialty Milling Recalls Multigrain Base Due to Metal Wire Mesh

    Dakota Specialty Milling is recalling Specialty Multigrain Base because it may contain pliable metal wire mesh fragments from a defective sifter.

    Product
    40145, SPECIALTY MULTIGRAIN BASE ( WHEAT BRAN, SUNFLOWER, WHEAT, OAT BRAN, RYE, OATS, OAT FLOUR, FLAXSEED, WHEAT GERM), DAKOTA SPECIALTY MILLING, INC., FARGO, ND , 1 Net WT 50 LBS.
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-1095-2013·2013-03-20

    Dakota Specialty Milling Recalls Sun Chip 6 Grain Blend Flour

    Dakota Specialty Milling is recalling Sun Chip 6 Grain Blend flour due to potential contamination with pliable metal wire mesh fragments from a defective sifter.

    Product
    41433, SUN CHIP 6 GRAIN BLEND( WHOLE MEAL: BROWN RICE, BUCKWHEAT AND QUINOA), DAKOTA SPECIALTY MILLING, INC., FARGO, ND , ----LBS.
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-1077-2013·2013-03-20

    Flour Blends Recalled Due to Potential Metal Wire Mesh Contamination

    Dakota Specialty Milling is recalling flour and flour blends that may contain pliable metal wire mesh fragments from a defective sifter.

    Product
    10073, Roman Meal Enhanced Healthy White Mix (sugarcane fiber, whole meal barley flour, white corn, wheat starch, oats, vitamins), Roman Meal Company, Tacoma, Washington, 1 Net WT 50 LBS.
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-1090-2013·2013-03-20

    Dakota Specialty Milling Recalls Flour Blends Due to Metal Wire Mesh Fragments

    Dakota Specialty Milling is recalling flour and flour blends that may contain pliable metal wire mesh fragments from a defective sifter.

    Product
    40632, SPECIALTY GRANNY GRAINS BLEND ( WHEAT BRAN, WHEAT, OATS , BARLEY, RYE), DAKOTA SPECIALTY MILLING, INC., FARGO, ND , 19 Net WT 40 LBS.
    Category
    Food
    Distribution
    21 states
  • HighCPSC·13144·2013-03-20

    Yuba Bicycles Recalls Mundo Cargo Bikes Due to Foot Injury Hazard

    Yuba Bicycles is recalling about 1,000 Mundo V4 cargo bikes because passengers' feet can get caught in the rear wheel. Consumers should stop using the bikes and contact the company for free wheel covers.

    Product
    Cargo Bikes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1125-2013·2013-03-20

    Dakota Specialty Milling Recalls Dark Rye Flour Due to Metal Wire Fragments

    Dakota Specialty Milling is recalling specific lots of Dark Rye Flour because they may contain pliable metal wire mesh fragments from a defective sifter.

    Product
    4060573 LOW MICRO. DARK RYE FLOUR (WHOLE RYE), DAKOTA SPECIALTY MILLING, INC., FARGO, ND, NET WT 50 LBS.
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-1076-2013·2013-03-20

    Dakota Specialty Milling Recalls Multigrain Flour Blend Due to Metal Wire Fragments

    Dakota Specialty Milling is recalling RM Multigrain W/Calcium Mixture because it may contain pliable metal wire mesh fragments from a defective sifter.

    Product
    10058-T, RM Multigrain W/Calcium Mixture - Thailand (wheat bran, yellow corn flour, oats, calcium carbonate, millet flour, yellow flax, stabilized wheat germ), Roman Meal Company, Tacoma, Washington, Net WT 20 KILOS.
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-1133-2013·2013-03-20

    Tausi Brand Salted Black Beans Recalled for Suspected Botulism

    Phil-Am Trading, Inc. is recalling Tausi Brand Salted Black Beans due to suspected, unconfirmed Clostridium botulinum contamination.

    Product
    Tausi Brand Salted Black Beans. Net Weight 180g (6.34 oz). Distributed by: V8 Commercial Co., Inc. San Juan, Metro Manila. Product of the Philippines.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1112-2013·2013-03-20

    Dakota Specialty Milling Recalls Oat Flour Due to Metal Wire Mesh Fragments

    Dakota Specialty Milling is recalling oat flour and flour blends that may contain pliable metal wire mesh fragments from a defective sifter.

    Product
    4060215, OAT FLOUR (OATS), DAKOTA SPECIALTY MILLING, INC., FARGO, ND , 0 NET WT. 50 LBS .
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-1107-2013·2013-03-20

    Dakota Specialty Milling Recalls Flour Blends Due to Metal Wire Mesh Contamination

    Dakota Specialty Milling is recalling specific flour and flour blends because they may contain pliable metal wire mesh fragments from a defective sifter.

    Product
    42207, FIBER PLUS BLEND POLY FREE ( ENRICHED WHEAT FLOUR RIBOFLAVIN, REDUCED IRON, THIAMINE MONONITRATE, NIACIN, FOLIC ACID, OAT BRAN, OAT FIBER, INULIN), DAKOTA SPECIALTY MILLING, INC., FARGO, ND , 19 NET WT. 50 LBS .
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-1144-2013·2013-03-20

    Whole Foods Recalls 365 Organic Orzo Due to Egg Allergen

    Whole Foods Market is recalling 365 Organic Orzo because testing detected egg protein in the product, posing a risk to individuals with egg allergies.

    Product
    365 Organic Orzo, 16oz, 20 carton/case
    Category
    Food
    Distribution
    10 states
  • HighFDA (Food)·F-1141-2013·2013-03-20

    Food For Life Recalls Ezekiel 4:9 Cereal for Undeclared Almond

    Food For Life Baking Company is recalling Ezekiel 4:9 Sprouted Grain Cereal because it may contain undeclared almonds, a common allergen.

    Product
    Ezekiel 4:9 Sprouted Grain Cereal- Original, 16 oz. Packaging label reads in part:"***Food FOR Life*** Ezekiel 4:9 SPROUTED WHOLE GRAIN CEREAL ORIGINAL NET WT. 16 OZ (454g)***MANUFACTURED BY: FOOD FOR LIFE BAKING COMPANY, INC. P.O. BOX 1434 CORONA, CA 92878-1434***".
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1097-2013·2013-03-20

    Dakota Specialty Milling Recalls 7 Grain Blend Flour Due to Metal Wire Fragments

    Dakota Specialty Milling is recalling 7 Grain Blend flour because it may contain pliable metal wire mesh fragments from a defective sifter.

    Product
    41511, 7 GRAIN BLEND - SOY FREE( WHEAT, WHEAT BRAN, RYE, BARLEY, TRITICALE, RICE FLOUR, OATS, CORN) DAKOTA SPECIALTY MILLING, INC., FARGO, ND , 19 NET WT. 50. LBS.
    Category
    Food
    Distribution
    21 states
  • HighFDA (Devices)·Z-0919-2013·2013-03-20

    Stryker Howmedica Command Instrument Broach Handle Recalled for Fracture Risk

    Stryker Howmedica is recalling 48 Command Instrument Broach Handles used in hip surgery due to reports of handle fracture and component disassociation.

    Product
    Command Instrument Broach Handle. Used in Total Hip Arthroplasty. Catalog Number: 6266-0-100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1131-2013·2013-03-20

    Golden Dharma Recalls Tausi Salted Black Beans Due to Botulism Risk

    Golden Dharma International is recalling Tausi Brand Salted Black Beans due to potential pathogen growth and toxin formation from Clostridium botulinum.

    Product
    Tausi Brand Salted Black Beans, 180g (6.34oz), 100 cans/carton This product is in a two piece can with a single seam. This 6.34 oz can is wrapped with a label containing, red, yellow, and black text labeled in part "Tausi Brand Salted Black Beans***Distributed by: V8…
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1123-2013·2013-03-20

    Dakota Specialty Milling Recalls Dark Rye Flour Due to Metal Wire Fragments

    Dakota Specialty Milling is recalling Dark Rye Flour and flour blends that may contain pliable metal wire mesh fragments from a defective sifter.

    Product
    4060570, DARK RYE FLOUR (RYE), DAKOTA SPECIALTY MILLING, INC., FARGO, ND NET WT 50 LBS..
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-1106-2013·2013-03-20

    Dakota Specialty Milling Recalls Multigrain Mix for Metal Wire Mesh Contamination

    Dakota Specialty Milling is recalling specific lots of multigrain mix due to potential contamination with pliable metal wire mesh fragments from a defective sifter.

    Product
    42204, MULTIGRAIN MIX FOR P.S. BREAD ( WHITE WHEAT, OATS, BARLEY, TRICALE, BROWN FLAX, CORN, SESAME SEED, POTATO FLAKES, WHEAT, RYE, WHEAT BRAN), DAKOTA SPECIALTY MILLING, INC., FARGO, ND , 1 NET WT. 50 LBS .
    Category
    Food
    Distribution
    21 states
  • ModerateFDA (Devices)·Z-0922-2013·2013-03-20

    Instratek Recalls Endotrig Trigger Release Blades Due to Cannula Advancement Issues

    Instratek is recalling 235 Endotrig Trigger Release Sterile Micro Hook Blades because they could not be advanced into the cannula during procedures.

    Product
    Endotrig Trigger Release Sterile Micro Hook Blade Product Usage: The blade is intended to release A-1 pulley in endoscopic trigger release procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0938-2013·2013-03-20

    Synthes Spine Pedicle Screw Recalled for Incorrect Length Etching

    Synthes USA HQ, Inc. is recalling 18 units of 45 mm Click 'X Pedicle Screws because they were incorrectly etched as 40 mm.

    Product
    Synthes Spine 5.2mm Titanium Click ' X Pedicle Screw Dual Core 40 mm Thread Length, Part Number 487.072. Intended to provide precise and segmental stabilization of the spine in skeletally mature patients.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Food)·F-1195-2013·2013-03-20

    King Arthur Flour Recalled Nationwide Due to Foreign Material Contamination

    The King Arthur Flour Company is recalling specific lots of 5-lb. Unbleached All-Purpose Flour nationwide because of foreign material contamination.

    Product
    King Arthur Unbleached All-Purpose Flour, 5-lb. bag UPC 0-71012-01050-9
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0932-2013·2013-03-20

    Spine Smith Partners Recalls Cynch Lordotic T-PLIF Implants Due to Marking Error

    Spine Smith Partners LP is recalling three Cynch Lordotic T-PLIF implants distributed in Texas because they were incorrectly laser marked as 23mm instead of 28mm.

    Product
    Cynch Lordotic T-PLlF Implant. Intervertebral fusion device with bone graft, for use with supplemental fixation.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0951-2013·2013-03-20

    Diagnostica Stago Recalls LIATEST VWF:Ag Coagulation Assay Kits

    Diagnostica Stago is recalling LIATEST VWF:Ag kits because measurement errors may lead to lowered percentage results.

    Product
    Vial Label: 1) LIATEST VWF:Ag Buffer - 5 ml Diagnostica Stago 2) LIATEST VWF:Ag Latex + 4 ml R3 Diagnostica Stago 3) LIATEST VWF:Ag Latex Diluent 4 mL Diagnostica Stago Model, catalogue, number 00518 - 58978 - 58979 Kit Label: LIATEST VWF:Ag DIAGNOSTICA STAGO…
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0941-2013·2013-03-20

    Synthes Large Combination Clamp Recalled Due to Oversized Hex Nuts

    Synthes USA is recalling 136 Large Combination Clamps because oversized hex nuts prevent standard 11 mm sockets and wrenches from fitting.

    Product
    Large Combination Clamp/Large External Fixation System, Part Number 390.005 Product Usage: Synthes Large External Fixation is intended for use to provide treatment for long bone and pelvic fractures that require external fixation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0950-2013·2013-03-20

    Philips Brilliance 64 and Ingenuity CT Systems Software Update Recall

    Philips Medical Systems is recalling 42 Brilliance 64 and Ingenuity CT systems to update software and customer release notes.

    Product
    Brilliance 64 and Ingenuity Computed Tomography X-Ray Systems The Brilliance 64 and Ingenuity CT are whole body 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…
    Category
    Medical Device
    Distribution
    19 states
  • ModerateFDA (Food)·F-1196-2013·2013-03-20

    King Arthur Unbleached Bread Flour Recalled for Foreign Material

    The King Arthur Flour Company is voluntarily recalling 5-lb bags of Unbleached Bread Flour nationwide due to the presence of foreign material.

    Product
    King Arthur Unbleached Bread Flour, 5-lb. bag UPC 0-71012-04105-3
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1067-2013·2013-03-20

    Yoruk Prens Rosehip Drink Mix Recalled for Unauthorized Colorants

    Ethnic International Holding Inc. is recalling Yoruk Prens Rosehip Drink Mix because it contains colorants not allowed in the USA.

    Product
    ROSEHIP DRINK MIX. Yoruk Prens Tarcin Kusburnu Net 400 g. USA Distributor: Ethnic Int. Holding Inc. 4 Corporate Drive, Cranbury, NJ 08512. Tel. 609-395-8513. Picture of flower on label.
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-0942-2013·2013-03-20

    Synthes Titanium Midface Distractor Recalled Due to Fit Issues

    Synthes USA is recalling 596 Titanium Midface Distractors because oversized tabs may prevent footplates from fitting properly.

    Product
    Synthes Titanium Midface Distractor, MR Conditional, Part number 487.982. For temporary stabilization and gradual lengthening of the cranial or midfacial bones.
    Category
    Medical Device
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-0935-2013·2013-03-20

    GE Healthcare Recalls MRI Systems Due to Reporting Tool Error

    GE Healthcare is recalling multiple MRI systems because an error in the SR Viewer Reporting Tool allows edits to be saved to incorrect reports.

    Product
    Optima MR450w, Discovery MR450, Discovery MR750, Signa HDx, Signa HDxt, Signa HDi, Signa Vibrant, and GE 1.5T Signa HDe MR System. The GE Signa HDx MR system is a whole body magnetic resonance scanner.
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0937-2013·2013-03-20

    Vygon Recalls 210 CT PICC Kits Packaged with Incorrect Needles

    Vygon Corporation is recalling 210 units of 6F Triple Lumen CT PICC kits because they were packaged with non-safety needles instead of the safety needles indicated on the label.

    Product
    Churchill Medical Systems, Inc. A Vygon Company - All sizes of CMS-CT6T225 6F Triple Lumen CT PICC with M.S.T. Components, Peripherally Inserted Central Catheter.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Food)·F-1062-2013·2013-03-20

    LYFE Kitchen Sweet Corn Chowder Recalled for Incorrect Packaging Sleeve

    LYFE Kitchen is recalling Sweet Corn Chowder because some containers were packaged in sleeves labeled for Orange Carrot Ginger Soup. The product itself is correctly labeled.

    Product
    LYFE Kitchen, Sweet Corn Chowder with Cashew Cream, Yukon Gold Potatoes and Bell Peppers; 28 oz. 680 gr, Keep Refrigerated. UPC 855764003527 Del Monaco Specialty Products, Morgan Hill, CA
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-1065-2013·2013-03-20

    Yoruk Prens Drink Mix Recalled for Prohibited Colorants

    Ethnic International Holding Inc. is recalling Yoruk Prens drink mix because it contains colorants not allowed in the USA.

    Product
    POMEGRANATE DRINK MIX. Yoruk Prens Nar Net 400 g. USA Distributor: Ethnic Int. Holding Inc. 4 Corporate Drive, Cranbury, NJ 08512. Tel. 609-395-8513. Picture of pomegranate on label.
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-0944-2013·2013-03-20

    Smith & Nephew Recalls Mislabelled Trigen Internal Hex Reconstruction Screws

    Smith & Nephew is recalling 90 units of Trigen internal hex reconstruction screws because 75 mm and 80 mm lengths were packaged in incorrect boxes and labels.

    Product
    INTERNAL HEX RECON SCREW, TI-6AL-4V, REF 7162375, TRIGEN (R) INTERNAL HEX CAPTURED RECON SCREW, QTY: (1), 6.4 MM, 75 MM, TITANIUM, Smith & Nephew, Inc. Orthopedic. Bone screw for intramedullary rod fixation.
    Category
    Medical Device
    Distribution
    11 states
  • ModerateFDA (Devices)·Z-0925-2013·2013-03-20

    Biomet Recalls Straight Acetabular Inserter Handles Due to Latch Interference

    Biomet, Inc. is recalling 58 non-sterile Straight Acetabular Inserter Handles because they may lock onto the cup during surgery, potentially causing delays.

    Product
    REF S313152 Straight Acetabular Inserter Handle Ringloc non-sterile Orthopedic manual surgical instrument
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0948-2013·2013-03-20

    Siemens CT Software Recall for Sporadic 3D Reconstruction Hang-Ups

    Siemens Medical Solutions is recalling 896 Somatom CT systems due to sporadic software malfunctions that cause 3D reconstructions to hang during preview.

    Product
    Siemens Somatom CTs equipped with software syngo CT2010A, syngo CT2010B, syngo CT2011A and CT2012B. Computed tomography x-ray system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0936-2013·2013-03-20

    Bacterin Elutia Silicone Surgical Wound Drain Recalled for Cracks

    Bacterin International is recalling specific lots of Elutia silicone surgical wound drains because a portion of the drain was found to be cracked.

    Product
    Bacterin Elutia, Hubless Coated Silicone Surgical Wound Drain 24 Fr Round Hubless, Full-Fluted Coated with Silver Sulfadiazine STERILE, Box of 10 Part #7118. Indicated for use in surgical wound drainage.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-192-2013·2013-03-20

    K C Pharmaceuticals Recalls Eye Drops With Incorrect Back Labeling

    K C Pharmaceuticals is recalling 31,704 bottles of Eye Drops advanced relief because the back labels fail to list three active ingredients.

    Product
    Eye Drops advanced relief (Dextran 70 0.1%, Polyethylene glycol 400 1%, Povidone 1%, Tetrahydrozoline HCl 0.05%) ophthalmic solution, 1/2 fl oz (15 mL) bottle, Distributed By Dolgencorp, LLC, 100 Mission Ridge, Goodlettsville, TN 37072.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1064-2013·2013-03-20

    Yoruk Prens Drink Mix Recalled for Prohibited Colorants

    Ethnic International Holding Inc. is recalling Yoruk Prens drink mix because it contains colorants not allowed in the USA.

    Product
    ORANGE DRINK MIX. Yoruk Prens Portalcal Net 400 g. USA Distributor: Ethnic Int. Holding Inc. 4 Corporate Drive, Cranbury, NJ 08512. Tel. 609-395-8513. Picture of orange on label.
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Food)·F-1139-2013·2013-03-20

    Koda Farms Recalls Sweet Rice Flour Due to Foreign Material Report

    Koda Farms is recalling specific lots of Mochiko Blue Star Sweet Rice Flour after a customer reported finding a hard yellow material in dough made with the product.

    Product
    Mochiko Blue Star Sweet Rice Flour, Net Wt 50 lb. or packaged in 1 lb bags. Koda Farms Milling, Inc. South Dos Palos, CA. 93665
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-1193-2013·2013-03-20

    Rose Valley Salted Print Butter Recalled for Antibiotic Testing Failure

    Farmers Cooperative Creamery is recalling Rose Valley Salted Print Butter because the milk used was not confirmed negative for antibiotics before processing.

    Product
    Salted Print Butter, Rose Valley brand. Product is packaged in 1 lb. unit package, 36 units per case. The UPC is 0 32395 09322 0. The product is labeled in parts: "***ROSE VALLEY***SWEET CREAM BUTTER***NET WT. 16OZ***MFD. BY FARMERS CO-OPERATIVE…
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0943-2013·2013-03-20

    Smith & Nephew Recalls Mislabelled Trigen Internal Hex Reconstruction Screws

    Smith & Nephew is recalling 69 Trigen internal hex reconstruction screws because 75 mm and 80 mm units were packaged in incorrect boxes and labels.

    Product
    INTERNAL HEX RECON SCREW, TI-6AL-4V, REF 7162380, TRIGEN (R) INTERNAL HEX CAPTURED RECON SCREW, QTY: (1), 6.4 MM, 80 MM, TITANIUM, Smith & Nephew, Inc. Orthopedic. Bone screw for intramedullary rod fixation.
    Category
    Medical Device
    Distribution
    11 states
  • ModerateFDA (Devices)·Z-0924-2013·2013-03-20

    Keystone Dental Recalls Mislabeled Genesis Straight Esthetic Abutments

    Keystone Dental Inc is recalling 22 units of Genesis Straight Esthetic abutments that were mislabeled with incorrect dimensions.

    Product
    Genesis Straight Esthetic 5.0 mm 3. mm Cuff Abutment Part Number: G71205 Genesis implant for single stage or two stage surgical procedures all types of of bone in partially or fully edentulous mandibles and maxillae.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1200-2013·2013-03-20

    Tausi Brand Salted Black Beans Recalled for Potential Botulism Risk

    G.L. Food Wholesale Inc. is recalling Tausi Brand Salted Black Beans due to potential pathogen growth and toxin formation from Clostridium botulinum.

    Product
    Tausi Brand Salted Black Beans, 180g (6.34oz), 100 cans/carton This product is in a two piece can with a single seam. This 6.34 oz can is wrapped with a label containing, red, yellow, and black text labeled in part "Tausi Brand Salted Black Beans***Distributed by: V8…
    Category
    Food
    Distribution
    9 states
  • ModerateFDA (Devices)·Z-0923-2013·2013-03-20

    Keystone Dental Recalls Mislabeled Genesis Straight Esthetic Abutments

    Keystone Dental Inc is recalling 35 units of Genesis Straight Esthetic abutments because they were mislabeled as 4.0 mm 1 mm cuff units when they are actually 5.0 mm 3 mm cuff units.

    Product
    Genesis Straight Esthetic 4.0 mm 1mm Cuff Abutment Part Number: G71200 Genesis implant for single stage or two stage surgical procedures all types of of bone in partially or fully edentulous mandibles and maxillae.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0929-2013·2013-03-20

    Abbott Recalls Mislabeled AMO Sensar Intraocular Lenses

    Abbott Medical Optics is recalling 155 AMO Sensar Intraocular Lenses because two production orders contained mislabeled units. The lenses are distributed worldwide.

    Product
    AMO Sensar Intraocular Lenses (IOLs), Model AR40e, Sensar Foldable IOL with OptiEdge Product Usage: These are ultraviolet-absorbing posterior chamber intraocular lenses for use after cataract extraction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-193-2013·2013-03-20

    Teva Recalls Terazosin Hydrochloride Capsules Due to Foreign Capsule Presence

    Teva Pharmaceuticals USA is recalling specific lots of Terazosin Hydrochloride Capsules because a foreign capsule was found in one bottle.

    Product
    Terazosin Hydrochloride Capsules, 2 mg, packaged in a) 100-count bottles (NDC 0093-4337-01); and b) 1000-count bottles (NDC 0093-4337-10), Rx only, Manufactured in India By: Intas Pharmaceuticals Ltd., Ahmedabad, Gujarat, India - 382 210; Manufactured For: Teva Pharmaceuticals…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1063-2013·2013-03-20

    Yoruk Prens Apple Drink Mix Recalled for Unapproved Colorants

    Ethnic International Holding Inc. is recalling Yoruk Prens drink mixes because they contain colorants not allowed in the USA.

    Product
    APPLE DRINK MIX. Yoruk Prens Elma Net 400 g. USA Distributor: Ethnic Int. Holding Inc. 4 Corporate Drive, Cranbury, NJ 08512. Tel. 609-395-8513. Picture of green apple on label.
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Food)·F-1066-2013·2013-03-20

    Yoruk Prens Drink Mix Recalled for Unauthorized Colorants

    Ethnic International Holding Inc. is recalling Yoruk Prens drink mix because it contains colorants not permitted in the USA.

    Product
    CINNAMON DRINK MIX. Yoruk Prens Tarcin Net 400 g. USA Distributor: Ethnic Int. Holding Inc. 4 Corporate Drive, Cranbury, NJ 08512. Tel. 609-395-8513. Picture of cinnamon sticks on label.
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-0927-2013·2013-03-20

    Innominata Lyme Disease Microplate EIA Kit Recalled for Low-Reactivity Issues

    Innominata dba GenBio is recalling 195 units of the Anti-Borrelia (Lyme) Microplate EIA Kit due to multiple incidents of low-reacting assay plates.

    Product
    ANTI-BORRELIA (LYME) MICROPLATE EIA Kit, Catalog # 32507 Kit Lot Number 120960. Package Insert Supplement: Calibrator-1206 U/mL, Positive Control-228 - 532 U/mL, and Negative Control-<120 U/mL; Manufactured by Innominata dba GenBio for Bio-Rad. The kit is used as an aid in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-200-2013·2013-03-20

    Fresenius Kabi Recalls Calcium Glucosate Injection Due to Missing Label

    Fresenius Kabi USA LLC is recalling 155,900 vials of Calcium Glucosate Injection, USP, 10% due to missing labels. The recall is nationwide.

    Product
    CALCIUM GLUCONATE INJECTION, USP, 10% (100 mg/mL), 10 mL, Single Dose Vial, Rx only, For Direct Slow IV or IV Additive Use Only, APP Pharmaceuticals, LLC Schaumburg, IL 60173 --- Product Code 31110, NDC 63323-311-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1130-2013·2013-03-20

    JMT Trading Recalls Tausi Salted Black Beans Due to Swollen Cans

    JMT Trading Company is recalling Tausi Salted Black Beans from the Philippines after reports of swollen cans. The product was distributed in the CA Bay area and Hawaii.

    Product
    Tausi Salted Black Beans, 180 gram (6.34 oz.) can. Ingredient: Black Beans, Water, Iodized salt, sugar and caramel. Distributed by V8 Commercial Co., Inc., San Juan, Metro Manila. Product of the Philippines. UPC 97399 00109
    Category
    Food
    Distribution
    1 state
  • LowFDA (Devices)·Z-0933-2013·2013-03-20

    Siemens Total Iron Binding Capacity Reagent Cartridge Recall for Labeling Error

    Siemens is recalling Total Iron Binding Capacity reagent cartridges because the stated analytical sensitivity in the instructions is no longer valid.

    Product
    Siemens Total Iron Binding Capacity (IBCT) Flex Reagent Cartridge. An in vitro diagnostic test intended to quantitatively measure Total Iron Binding Capacity in human serum.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·13142·2013-03-19

    Lighting Science Group Recalls LED Light Bulbs Due to Fire Hazard

    Lighting Science Group is recalling approximately 554,000 LED light bulbs sold under Definity, EcoSmart, Sylvania, and Westinghouse brands because they can overheat and pose a fire hazard.

    Product
    LED Light Bulbs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·13V100000·2013-03-19

    Starcraft XLT Buses Recalled for Incorrect Weight Rating Labels

    Starcraft Bus is recalling 2004-2009 XLT buses because incorrect weight rating labels could lead to improper loading and tire failure.

    Product
    STARCRAFT — STARCRAFT XLT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V095000·2013-03-15

    Nissan Recalls 2012-2013 NV Models Due to Transmission Shift Lever Defect

    Nissan is recalling 2012-2013 NV vehicles because an incorrectly installed clip may cause the gear indicator to mismatch the actual gear position, increasing the risk of the vehicle rolling away.

    Product
    NISSAN — NISSAN NV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V097000·2013-03-15

    GM Recalls 2013 Buick LaCrosse and Cadillac SRX for Transmission Software Issue

    General Motors is recalling 2013 Buick LaCrosse and Cadillac SRX vehicles because a software defect may cause the transmission to shift to Sport mode, removing engine braking and increasing crash risk.

    Product
    BUICK — BUICK, CADILLAC LACROSSE, SRX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V098000·2013-03-15

    Toyota Recalls FJ Cruiser Models Due to Seat Belt Anchor Defect

    Toyota is recalling 2007-2013 FJ Cruisers because cracks in the rear door panel may cause the front seat belt retractors to detach, increasing injury risk in a crash.

    Product
    TOYOTA — TOYOTA FJ CRUISER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V093000·2013-03-15

    Acura TSX vehicles are recalled due to engine-stall risk

    Honda is recalling certain 2004-2008 Acura TSX vehicles sold in or registered in specified states. Corrosion can damage the engine control unit and potentially cause the engine to stall, increasing crash risk.

    Product
    ACURA — ACURA TSX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V092000·2013-03-14

    Honda Recalls 2005-2006 Acura and Honda Vehicles for VSA Defect

    Honda is recalling specific 2005-2006 Acura MDX, RL, and Honda Pilot vehicles because a defective capacitor may cause sudden, inadvertent braking.

    Product
    ACURA — ACURA, HONDA MDX, RL, PILOT
    Category
    Vehicle
    Distribution
    Distributed nationwide

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