The Recall Desk

Archive

July 2012 recalls

445 recalls were announced in July 2012.

What the numbers show

Critical
14
Severe
94
High
219
Moderate
91
Low
27

Of the 445 recalls this month scored against our rubric, 3% are Critical, 21% are Severe.

301–400 of 445

  • ModerateFDA (Food)·F-1713-2012·2012-07-11

    Frozen Korean Oysters Recalled Due to Shipper Certification Issues

    Seoul Shik Poom, Inc. is recalling 412 cases of frozen oysters because the shippers were delisted from the FDA's International Certification System.

    Product
    Frozen Oysters, Net Wt 1 LBS (454g). Distributed by: Seoul Shik Poom, Engleside, NJ. Origin: Republic of Korea.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1407-2012·2012-07-11

    Sanofi Recalls Eloxatin Injection Due to Manufacturing Practice Deviations

    Sanofi-aventis is recalling 196,355 vials of Eloxatin (oxaliplatin) injection nationwide because the contract manufacturer failed to meet Good Manufacturing Practices.

    Product
    Eloxatin (OXALIplatin injection) 5 mg/mL Injection, 50 mg, Rx only, Mfd. for: sanofi aventis US LLC Bridgewater, NJ 08807, NDC 0024-0590-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1712-2012·2012-07-11

    Rosati Watermelon Water Ice Recalled for Undeclared Yellow Dye

    SR Rosati, Inc. is recalling Rosati Cry Baby Sour Watermelon water ice because the label does not declare FD&C Yellow #5.

    Product
    Rosati Cry Baby Sour Watermelon water ice, 6 fl oz
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Food)·F-1715-2012·2012-07-11

    FDA Recalls Korean Whole Oysters Due to Potential Water Pollution

    Mitsui Foods Inc. is recalling two brands of whole oysters from Korea because Korean waters may be polluted. Consumers should stop eating these products.

    Product
    Whole Oysters: 1) Empress Whole Oysters, NET WT 8 OZ. Distributed By Mitsui Foods Inc. Norwood NJ 07648 Product of Korea, UPC 7360000719. 2) Premium Quality Private Selection Whole Oysters, NET WT 8 OZ. Distributed By Inter-American Products, Inc. Cincinnati, OH 45202. Produc
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1408-2012·2012-07-11

    Sanofi-aventis Recalls Eloxatin Injection Due to Manufacturing Issues

    Sanofi-aventis is recalling Eloxatin (oxaliplatin) injection vials because the contract manufacturer had significant Good Manufacturing Practice issues.

    Product
    Eloxatin (OXALIplatin injection) 5 mg/mL injection, 100 mg, Rx only, Mfd. for: sanofi aventis US LLC Bridgewater, NJ 08807, NDC 0024-0591-20
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1927-2012·2012-07-11

    Thayer Medical Recalls AirLife MiniSpacer MDI Adapters Due to Molding Defect

    Thayer Medical is recalling 19,340 AirLife MiniSpacer MDI adapters due to a molding defect that may result in incomplete filling of the aerosol dispensing pathway.

    Product
    AirLife¿ MiniSpacer¿ MDI Dispenser Adapter. Dual-Spray MiniSpacer¿ Metered Dose Inhaler (MDI) Dispenser/Adapter with 15 mm connections. The 15 mm Dual Spray MiniSpacer¿ is a Metered Dose Inhaler (MDI) Dispenser. It is a non-sterile, single-use item, intended to dispense aeros
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Food)·F-1714-2012·2012-07-11

    Frozen Salted Clam Recalled Due to Shipper Certification Issues

    Seoul Shik Poom, Inc. is recalling 3 cases of Frozen Salted Clam because the shippers were delisted from the ICSSL.

    Product
    Frozen Salted Clam, 12/210g. Distributed by: Seoul Shik Poom, Engleside, NJ. Origin: Republic of Korea.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1942-2012·2012-07-11

    Philips Xcelera Connect Software Recalled for Incomplete Data Exchange

    Philips Healthcare is recalling 226 units of Xcelera Connect software because unformatted reports may result in incomplete information arriving at the interface.

    Product
    Philips Xcelera Connect, Software R2.1 L 1 SP2, an interface engine for data exchange. Philips Xcelera Connect R2.x is a generic interface and data mapping engine between a Hospital Information System (HIS), Imaging Modalities, Xcelera PACS and Xcelera Cath Lab Manager (CLM).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1941-2012·2012-07-11

    Pride Mobility Victory 9 Wheelchair Recalled for Harness Sealing Defect

    Pride Mobility is recalling 186 Victory 9 motorized wheelchairs because the main harness connector lacks required back shield sealing, allowing water to seep through.

    Product
    Victory 9 with Power Seat (SC609PS) Motorized wheelchair with elevating seat.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Food)·F-1701-2012·2012-07-11

    Mexican Sweet Bread Recalled for Undeclared Yellow 6

    Mexicantown Wholesale is recalling 26 units of Empanadas de Pina (Mexican Sweet Bread) due to undeclared Yellow 6.

    Product
    1) EMPANADAS DE PINA (MEXICAN SWEET BREAD) IMPORTED BY EL CHARRO MEXICANTOWN BAKERY DETROIT MI 48210 3.4oz 21-MAY-12, UPC: 9564000009 2) EMPANADAS DE PINA (MEXICAN SWEET BREAD/pain sucre) IMPORTED BY FIESTA WHOLESALE 226-440-3033 MY LITTLE MEXICO 3.4oz
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-1703-2012·2012-07-11

    Mexican Sweet Bread Recalled for Undeclared Red 40 Dye

    Mexicantown Wholesale recalled 26 units of Mexican Sweet Bread for containing undeclared Red 40 dye. The products were distributed in Canada.

    Product
    EMPANADAS DE FRESA (MEXICAN SWEET BREAD) IMPORTED BY EL CHARRO MEXICANTOWN BAKERY DETROIT MI 48210 3.4oz 21-MAY-12
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-1724-2012·2012-07-11

    Aldi Recalls Canned Oysters Due to Insanitary Conditions

    Aldi is recalling specific lots of canned oysters because they were prepared under insanitary conditions that may have contaminated the product.

    Product
    Northern Catch Harvest of the Sea Fancy Whole Oysters and SeaNet Fancy Whole Oysters; Net Wt. 8 oz (227g) cans, 12 cans per carton; Distributed by Aldi Inc., Batavia, IL 60510-1477; Product of Korea; UPC 0 41498 11984 3
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1409-2012·2012-07-11

    Teva Recalls Metoprolol Tartrate Tablets Due to Weight Variations

    Teva Pharmaceuticals is recalling 2,268 bottles of Metoprolol Tartrate 50 mg tablets in Ohio because some tablets may not meet weight specifications.

    Product
    Metoprolol Tartrate Tablets USP 50 mg, 1000 count bottle, Rx only, Manufactured in india By: Emcure Pharmaceuticals LTD. Hinjwadi, Pune, India, Manufactured for TEVA Phamaceuticals USA, Sellersville, PA 18960, NDC 0093-0733-10
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Food)·F-1716-2012·2012-07-11

    Mitsui Foods Recalls Korean Smoked Oysters Due to Import Block

    Mitsui Foods Inc. is recalling specific lots of Empress and Private Selection smoked oysters because Korean shellfish imports were blocked by the FDA due to potential water pollution.

    Product
    Smoked Oysters: 1) Empress Smoked Oysters In Cottonseed Oil, NET WT 3.75 OZ. Distributed By Mitsui Foods Inc. Norwood NJ 07648 Product of Korea, UPC7360000713. 2) Premium Quality Private Selection Smoked Oysters In Cottonseed Oil, NET WT 3.75 OZ. Distributed By Mitsui Foods In
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1638-2012·2012-07-11

    Dannon Fruit on the Bottom Yogurt Recalled for Coliforms

    The Dannon Company is recalling specific lots of Fruit on the Bottom Raspberry yogurt due to routine testing that detected coliforms.

    Product
    Dannon Fruit on the Bottom, Raspberry flavor. 6oz form fill seal cup yogurt with predominantly blue labelling.
    Category
    Food
    Distribution
    3 states
  • LowFDA (Drugs)·D-1399-2012·2012-07-11

    Watson Loxapine Capsules Recalled for Outdated Patient Outsert

    Watson Laboratories is recalling 8,254 bottles of Loxapine Capsules 5mg because an outdated patient outsert was used during packaging.

    Product
    Loxapine Capsules USP, 5mg, 100 count bottle, Rx only Manufactured By: Watson Laboratories Inc., Corona, CA 92880 NDC # 00591-0369-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1406-2012·2012-07-11

    Health Plus Super Colon Cleanse Recalled for Labeling Error

    Health Plus Incorporated is recalling Super Colon Cleanse capsules because the Drug Facts label incorrectly describes the active ingredient per dose instead of per capsule.

    Product
    Super Colon Cleanse, stimulant laxative, 140 mg of Senna per capsule, 25 doses, 100 capsules, Manufactured by: healthPLUS Inc. Chino, CA 91710 USA.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1405-2012·2012-07-11

    Ranbaxy Recalls Subpotent Balnetar Therapeutic Tar Bath Coal Tar Product

    Ranbaxy Inc. is recalling Balnetar Therapeutic Tar Bath, Coal Tar USP 2.5%, because the product failed to meet specifications for coal tar content.

    Product
    Balnetar Therapeutic Tar Bath, Coal Tar USP 2.5% (from Coal Tar USP Solution, 7%), 7.5 oz bottle, Distributed by Ranbaxy, Jacksonville, FL 32257, NDC 10631-106-08
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1403-2012·2012-07-11

    Watson Recalls Loxapine Succinate Capsules Due to Outdated Patient Outsert

    Watson Laboratories is recalling 7,262 bottles of Loxapine Succinate Capsules because an outdated patient outsert was used during packaging.

    Product
    Loxitane Capsules, Loxapine Succinate Capsules, 10mg base, 100 count bottle, Rx only, Watson Laboratories Inc., Corona, CA 92880 NDC # 52544-495-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1639-2012·2012-07-11

    Dannon Mixed Berry Yogurt Recalled for Routine Coliform Testing

    The Dannon Company Inc is recalling 1,350 cases of Dannon Fruit on the Bottom Mixed Berry yogurt due to routine testing showing the presence of Coliforms.

    Product
    Dannon Fruit on the Bottom, Mixed Berry flavor. 6oz form fill seal cup yogurt with predominantly blue labelling.
    Category
    Food
    Distribution
    3 states
  • LowFDA (Drugs)·D-1402-2012·2012-07-11

    Watson Recalls Loxapine Capsules Due to Outdated Patient Outsert

    Watson Laboratories is recalling 18,902 bottles of Loxapine 50mg capsules because an outdated patient outsert was used during packaging.

    Product
    LOXAPINE — LOXAPINE (LOXAPINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1404-2012·2012-07-11

    Imodium Multi-Symptom Relief Caplets Recalled for Defective Containers

    McNeil Consumer Healthcare is recalling Imodium Multi-Symptom Relief Caplets due to defective containers and damaged blister units.

    Product
    Imodium Multi-Symptom Relief Caplets, Loperamide HCl 2 mg/Simethicone 125 mg, 18 count blister pack cartons, McNeil Consumer Healthcare, Div of McNeil-PPC Inc., Fort Washington, PA
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1943-2012·2012-07-11

    Integra Recalls Single Shot Epidural Trays Missing Injectable Components

    Integra LifeSciences is recalling one lot of Single Shot Epidural Trays because they were shipped without required injectable components.

    Product
    Single Shot Epidural Trays, Sterile, Integra Pain Management, West Valley City, Utah 84119, each kit contains sterile instruments, drugs and other medical materials that will support the administration of spinal anesthesia for use by a surgeon, nurse or other licensed medical pro
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V324000·2012-07-10

    NABI Recalls 2003-2011 45CLFW Buses for Steering Gear Defect

    North American Bus Industries is recalling 339 transit buses due to a loose steering connection that could cause loss of control.

    Product
    NABI — NABI 45CLFW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·12218·2012-07-10

    Bosch Recalls SkilSaw Miter Saws Due to Laceration Hazard

    Bosch is recalling approximately 22,149 SkilSaw 10-inch compound miter saws because the lower guard can break and contact the blade, posing a laceration hazard.

    Product
    Miter Saw
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V323000·2012-07-09

    Van Hool Recalls 2011-2012 TD925 Motorcoaches for Driver Seat Defect

    Van Hool is recalling 152 model year 2011-2012 TD925 motorcoaches because an incorrect driver's seat riser and floor adapter plate were installed, increasing injury risk in a crash.

    Product
    VAN HOOL — VAN HOOL TD925
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·12V321000·2012-07-09

    Glaval Buses Recalled for Wheelchair Lift Roll Stop Latch Defect

    Glaval is recalling certain buses equipped with Braun wheelchair lifts because roll stop latches may become bent or misaligned, posing a fall risk to occupants.

    Product
    GLAVAL — GLAVAL, GLAVAL BUS TITAN, CONCORDE II, TITAN II, SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V315000·2012-07-06

    Prevost Recalls 2007-2009 X3-45 Coaches Due to Fire Risk

    Prevost is recalling 428 model year 2007-2009 X3-45 coaches because a missing protective sleeve on a battery cable could cause a short-circuit and fire.

    Product
    PREVOST — PREVOST X3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V318000·2012-07-06

    Ford Recalls 2012 F-650 and F-750 Trucks for Windshield Bonding Defect

    Ford is recalling 783 model year 2012 F-650 and F-750 trucks because missing primer on the windshield may cause it to separate from the cab, increasing injury risk.

    Product
    FORD — FORD F-650, F-750
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V317000·2012-07-06

    Volvo Recalls 2011-2013 S80 Vehicles for Transmission Software Error

    Volvo is recalling 2011-2013 S80 vehicles because a software error may prevent the transmission from downshifting, potentially causing an engine stall and increasing crash risk.

    Product
    VOLVO — VOLVO S80
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V313000·2012-07-05

    Volvo Bus 9700 Recall for Improperly Secured Passenger Seat Tracks

    Prevost Cars is recalling 2009-2011 Volvo Bus 9700 models because passenger seat wall mounting tracks may not be properly secured, increasing injury risk in a crash.

    Product
    VOLVO BUS — VOLVO BUS 9700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V314000·2012-07-05

    Navistar Recalls 2008 Safari Coach Simba Diesel for Brake Defect

    Navistar is recalling one 2008 Safari Coach Simba Diesel motorhome because brake calipers may grow, causing drag and reduced performance.

    Product
    SAFARI COACH — SAFARI COACH SIMBA DIESEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1682-2012·2012-07-04

    TWI Foods Coconut Cookies Recalled for Undeclared Milk

    Singh And Singh Distributors Inc. is recalling Crispy by TWI Foods Coconut Cookies because they may contain undeclared milk.

    Product
    Crispy by TWI Foods Coconut Cookies, Biscuit, Net Wt 200 g, Product of Canada Manufactured by TWI Foods Inc. 2600 Drew Road, Mississauga, Ont, Canada L4T 3M5.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1671-2012·2012-07-04

    Ballas Egg Prod Corp Recalls Pasteurized Liquid Whole Eggs

    Ballas Egg Prod Corp is recalling pasteurized liquid whole eggs that tested positive for Salmonella. The product was distributed to Ohio and South Carolina.

    Product
    Pasteurized liquid whole eggs
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-1679-2012·2012-07-04

    Crispy Almond Cake Rusk Recalled for Undeclared Milk Allergen

    Singh And Singh Distributors Inc. is recalling Crispy Almond Cake Rusk nationwide because the product may contain undeclared milk.

    Product
    Crispy by TWI Foods Almond Cake Rusk, Biscotte Croustillante Almande, Net Wt 750 g, Product of Canada Manufactured by TWI Foods Inc. 1869 Gage Court, Mississauga, Ont, Canada L5S 1S3.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1672-2012·2012-07-04

    FDA Recalls Frozen Clam Meat Due to Norovirus Contamination

    Grand Supercenter Inc. is recalling frozen seasoned clam meat because it may be contaminated with norovirus due to insanitary conditions.

    Product
    Frozen Seasoned and Cooked Clam Meat with Hot Pepper (Item #33229120) (5kg X 2).
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1673-2012·2012-07-04

    Grand Supercenter Recalls Frozen Oysters Due to Norovirus Contamination

    Grand Supercenter Inc. is recalling frozen oysters nationwide because inspectional evidence and illness reports indicate the products were prepared under insanitary conditions and may be contaminated with norovirus.

    Product
    Frozen Oysters: 1) I.Q.F. 2 LB/12 Frozen Oyster (Permit #NJ36RS) - Item #33200115.; I.Q.F. (T-Size) 8 oz/40 Frozen Oyster (Permit #NJ36RS) - Item #33200116; BLOCK 1 LB/30 Frozen Oyster (Permit #NJ36RS) - Item #33200117. I.Q.F. (S Size) 5 LB/6 Frozen Oyster (Permit #NJ36RS) - It
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1893-2012·2012-07-04

    Terumo Recalls Sarns Antegrade Cardioplegia Cannula Kits Due to Foreign Substance

    Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannula kits because a foreign substance was found on the inner surface of some cannula tips that could dislodge.

    Product
    CPB CATHETER KIT-DR VANTRIGHT Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1395-2012·2012-07-04

    Lloyd Inc Recalls Subpotent Thyro-Tab 0.75 mg Tablets

    Lloyd Inc is recalling 1,913,236 Thyro-Tab 0.75 mg tablets because they failed potency testing at the 6-month interval.

    Product
    Thyro-Tab.075 mg., packaged in bulk drums for repackaging. The firm name on the label is Lloyd Pharmaceutical, Shenandoah, Iowa 51601.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1651-2012·2012-07-04

    CJ Foods Recalls Frozen Oysters Due to Insanitary Conditions

    CJ Foods is recalling specific lots of CJ Het Oyster frozen oysters because they were prepared or held under insanitary conditions, posing a potential health risk.

    Product
    CJ Het Oyster (CJ Frozen Oyster), 40x8oz.. Material#912329, Frozen Oyster (KR 12 SP 050110), Material#912330, Frozen Oyster (KR 12 SP 050210), Material#912331, Frozen Oyster (KR 12 SP 050310).
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Devices)·Z-1884-2012·2012-07-04

    Terumo Recalls Sarns Antegrade Cardioplegia Cannulas Due to Foreign Substance

    Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannulas because a foreign substance was found on the inner surface of some cannula tips that can be dislodged.

    Product
    X-COATED SMALL PATIENT PACK Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during c
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1883-2012·2012-07-04

    Terumo Recalls Sarns Antegrade Cardioplegia Cannula Due to Foreign Substance

    Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannulas because a foreign substance on the inner surface of some tips can be dislodged.

    Product
    X-COATED SMALL PATIENT PACK Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during c
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1653-2012·2012-07-04

    Nishimoto Recalls Shirakiku Brand Breaded Oysters Due to Insanitary Conditions

    Nishimoto Trading Co Ltd is recalling Shirakiku Brand breaded oysters nationwide because they were prepared or held under insanitary conditions, posing a potential health risk.

    Product
    Oysters Breaded/Kaki Fry, 12x2lbs, item #88250, SK Breaded Oyster 10x2lb, item#91750, and Oyster Breaded Big KOR SK F, item#91306.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1881-2012·2012-07-04

    Terumo Recalls Sarns Antegrade Cardioplegia Cannula Due to Foreign Substance

    Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannulae because a foreign substance was found on the inner surface of some tips that could be dislodged.

    Product
    XC HEART/LUNG PACK W/SX25RX Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during c
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1882-2012·2012-07-04

    Terumo Recalls Sarns Antegrade Cardioplegia Cannula Due to Foreign Substance

    Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannulas because a foreign substance was found on the inner surface of some tips that could dislodge.

    Product
    X-COATED TRANSPLANT PACK Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during card
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1654-2012·2012-07-04

    PGP International Recalls iForce Nutrition Protein Powder for Undeclared Wheat

    PGP International is recalling iForce Nutrition PROTEAN Lean Protein powder because it contains undeclared wheat. The product was distributed in California, North Carolina, and Wisconsin.

    Product
    iForce Nutrition Xtreme Series, PROTEAN, Lean Protein, Strawberry Creamsicle, Dietary Supplement, 4 lbs. Mfg. for Dist by, Tribravus Enterprises, LLC, Vista, CA 92081
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1894-2012·2012-07-04

    Terumo Recalls Sarns Antegrade Cardioplegia Cannula Kits Due to Foreign Substance

    Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannula kits because a foreign substance on the cannula tips can be dislodged during use.

    Product
    CPB CATHETER KIT-DR BARTLES Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during c
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1646-2012·2012-07-04

    Bay Valley Foods Recalls Pasta Mix Due to Metal Fragments

    Bay Valley Foods is voluntarily recalling boxed pasta mix products because they contain a seasoning blend that may have small metal fragments.

    Product
    H.E.B Pasta Salad Ranch & Bacon, NET WT 7.5 OZ , CONT. NET 212G, UPC 4122089106
    Category
    Food
    Distribution
    25 states
  • HighFDA (Devices)·Z-1865-2012·2012-07-04

    GE OEC Uroview 2800 Recalled for Intermittent Safety Issues

    GE OEC Medical Systems is recalling 717 OEC Uroview 2800 fluoroscopic imaging systems due to intermittent safety issues, including navigation tracking inaccuracy and system lock-ups.

    Product
    OEC Uroview 2800, Model number A349855. Designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical, and interventional procedures.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1650-2012·2012-07-04

    Bay Valley Foods Recalls Macaroni and Cheese for Metal Fragments

    Bay Valley Foods is voluntarily recalling Great Value Macaroni and Cheese because the seasoning blend may contain small metal fragments.

    Product
    Great Value, Thick and Creamy Macaroni and Cheese , NET WT 7.25 OZ (206g), UPC 7874223061, DISTRIBUTED BY: Wal-Mart Stores, Inc., Bentonville, AR 72716
    Category
    Food
    Distribution
    25 states
  • HighFDA (Devices)·Z-1887-2012·2012-07-04

    Terumo Recalls Sarns Antegrade Cardioplegia Cannulas Due to Foreign Substance

    Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannulas because a foreign substance was found on the inner surface of some tips that can be dislodged.

    Product
    X-COATED H/L PK W/FX15RW40 Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during ca
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1858-2012·2012-07-04

    Hartmann Sterilux Gauze Sponges Recalled for Sterile Barrier Defects

    Hartmann USA is recalling Sterilux gauze sponges because micro holes were found in the sterile barrier, potentially compromising sterility.

    Product
    Hartmann Sterilux Ref 56910000 Sterile Premium gauze sponge 4"x4" 12-ply 24 boxes/case 1200 total sponges For use in wound cleansing, debriding of wounds, wound packing, covering and swabbing
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1641-2012·2012-07-04

    Pasta Roni Recalled for Potential Metal Fragment Contamination

    Quaker Foods and Snacks North America is recalling specific Pasta Roni products due to potential metal fragment contamination in an ingredient.

    Product
    Pasta Roni Parmesan Cheese Flavor angel hair pasta in a Parmesan sauce with other natural flavors; Net Wt. 5.1 oz. box/12 boxes/case; Distributed by Golden Grain Co., P.O. Box 049003, Chicago, IL 60604-9903; UPC 0 15300 44049
    Category
    Food
    Distribution
    13 states
  • HighFDA (Food)·F-1680-2012·2012-07-04

    TWI Foods Pistachio Cookies Recalled for Undeclared Milk and Almonds

    Singh And Singh Distributors Inc. is recalling TWI Foods Pistachio Cookies because they may contain undeclared milk and almonds.

    Product
    Crispy by TWI Foods Pistachio Cookies, Biscuit, Net Wt 400g, Product of Canada Manufactured by TWI Foods Inc. 1869 Gage Court, Mississauga, Ont, Canada L5S 1S3.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1648-2012·2012-07-04

    Bay Valley Foods Recalls Macaroni and Cheese for Metal Fragments

    Bay Valley Foods is voluntarily recalling Kroger Macaroni & Cheese Three Cheese because the seasoning blend may contain small metal fragments.

    Product
    Kroger, Macaroni & Cheese Three Cheese, NET WT 7.25 OZ (205 g), UPC 1111085146, Distributed by The Kroger Co., Cincinnati, OH 45202.
    Category
    Food
    Distribution
    25 states
  • HighFDA (Food)·F-1676-2012·2012-07-04

    Crispy Almond Cookies Recalled for Undeclared Milk Allergen

    Indian Foods & Spices, LLC is recalling Crispy by TWI Foods Almond Cookies because the product may contain undeclared milk.

    Product
    Crispy by TWI Foods Almond Cookies, Biscuit, Net Wt 400 g, Product of Canada Manufactured by TWI Foods Inc. 2600 Drew Roadt, Mississauga, Ont, Canada L4T 3M5.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1875-2012·2012-07-04

    Terumo Recalls Sarns Antegrade Cardioplegia Cannulas Due to Foreign Substance

    Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannulas because a foreign substance found on the inner surface of some tips can be dislodged during use.

    Product
    Sarns Antegrade Cardioplegia Cannula: ROOT INFUSTION VENT CATHETER WITH 12 GAUGE BLUE NEEDLE RECTANGULAR FLANGE, 6" (15 CM) LONG Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1859-2012·2012-07-04

    Stryker Recalls GoBed+ Model FL20E Hospital Beds Due to Scale Failures

    Stryker is recalling 6,325 GoBed+ Model FL20E hospital beds worldwide because loadcell failures can cause scale errors or disable bed exit functions.

    Product
    GoBed+ . Model FL20E Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of th
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1878-2012·2012-07-04

    Terumo Recalls Sarns Antegrade Cardioplegia Cannulas Due to Foreign Substance

    Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannulas because a foreign substance was found on the inner surface of some tips that could be dislodged.

    Product
    SARNS ANTEGRADE CARDIOPLEGIA CANNULA: ROOT INFUSION CANNULA WITH 12-GAUGE BLUE NEEDLE,RECTANGULAR FLANGE AND SUTURE COLLAR, 6" (15CM) LONG Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver c
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1891-2012·2012-07-04

    Terumo Recalls Sarns Cardioplegia Cannulas Due to Foreign Substance

    Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannulas because a foreign substance was found on the inner surface of some tips that can be dislodged.

    Product
    CPB CATHETER KIT- DR HENDRICKSO Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta duri
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1885-2012·2012-07-04

    Terumo Recalls Sarns Cardioplegia Cannulas Due to Foreign Substance

    Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannulas because a foreign substance was found on the inner surface of some tips that can be dislodged.

    Product
    MAYO MN XCOATED 3/8X1/2 AV Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during ca
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1897-2012·2012-07-04

    Ethicon Surgiflo Hemostatic Matrix Kit Recalled for Potential Non-Sterility

    Ethicon is recalling Surgiflo Hemostatic Matrix Kits with Thrombin because an undetected air leak during manufacturing may have compromised the sterility of the thrombin component.

    Product
    Ethicon Surgiflo Hemostatic Matrix Kit with Thrombin Plus Flex Tip Distributed by Ethicon Ethicon Inc., Somerville, NJ 08876 USA Manufactured by Ferrosan Medical Devices Ferrosan Medical Devices A/S Sydmarken 5, DK-2860 Soeberg, Denmark Mixed with sterile saline or thromb
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1867-2012·2012-07-04

    Siemens BCS Behring Coagulation System Recalled for Potential Test Errors

    Siemens Healthcare Diagnostics is recalling 186 BCS Behring Coagulation Systems because a specific sequence of tests may result in shortened clotting times.

    Product
    BCS(R) Behring Coagulation System, Device catalog No. OVIO03 Product Usage: Multipurpose system for In Vitro coagulation studies
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1649-2012·2012-07-04

    Bay Valley Foods Recalls Macaroni and Cheese Due to Metal Fragments

    Bay Valley Foods is voluntarily recalling approximately 74,000 cases of boxed pasta mix products because they may contain small metal fragments.

    Product
    Meijer Macaroni & Cheese Dinner Thick"n Cheesy, NET WT 7.25 OZ (206 g), UPC 4125096335, DIST. BY MEIJER DISTRIBUTION INC. GRAND RAPIDS, MI 49544
    Category
    Food
    Distribution
    25 states
  • HighFDA (Devices)·Z-1880-2012·2012-07-04

    Terumo Recalls Sarns Cardioplegia Cannulas Due to Foreign Substance

    Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannulas because a foreign substance on the inner surface of the tips can be dislodged during use.

    Product
    INDIANA/OHIO HEART Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during cardiopulm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1864-2012·2012-07-04

    Hill-Rom Recalls Advanta 2 Hospital Beds Due to Siderail Screw Stripping

    Hill-Rom is recalling 7,843 Advanta 2 hospital beds because screws used to attach siderails were found to be stripping from the plastic cavity.

    Product
    Advanta 2 Bed. The Advanta 2 Bed is intended for low to moderate acuity patients in the medical/surgical area of the hospital.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1857-2012·2012-07-04

    Hartmann Sterile Gauze Sponges Recalled for Sterile Barrier Defects

    Hartmann USA is recalling specific lots of Econolux sterile gauze sponges because micro holes were detected in the sterile barrier system, potentially compromising sterility.

    Product
    Hartmann Econolux Ref 416 105 Sterile Gauze sponge 4"x4" 12-ply 24 boxes/case 1200 total sponges For use in wound cleansing, debriding of wounds, wound packing, covering and swabbing
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1877-2012·2012-07-04

    Terumo Recalls Sarns Antegrade Cardioplegia Cannulas Due to Foreign Substance

    Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannulas because a foreign substance was found on the inner surface of some tips that could be dislodged.

    Product
    SARNS ANTEGRADE CARDIOPLEGIA CANNULA: ROOT INFUSION CANNULA WITH 14-GAUGE WHITE NEEDLE,RECTANGULAR FLANGE AND SUTURE COLLAR, 6" (15CM) LONG Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1869-2012·2012-07-04

    Siemens B12 Reagent Cartridges Recalled for False Test Results

    Siemens is recalling B12 Flex reagent cartridges because Intrinsic Factor Blocking Antibodies can cause false high Vitamin B12 results.

    Product
    Siemens Dimension Vista(R) System B12 Flex(R) Reagent Cartridge (K6442) B12 Flex Reagent Cartridge used with the Dimension Vista System for the in vitro diagnostic test for the quantitative measurement of Vitamin B12 in human serum and plasma.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1826-2012·2012-07-04

    Fresenius NaturaLyte Liquid Acid Concentrate Recalled for Alkalosis Risk

    Fresenius Medical Care is recalling NaturaLyte Liquid Acid Concentrate due to a risk of alkalosis. The product is used for hemodialysis.

    Product
    Fresenius NaturaLyte Liquid Acid Concentrate Product Codes: 08-0231-4, 08-1001-0, 08-1201-8, 08-1231-3, 08-1251-1, 08-1301-4, 08-2201-5, 08-2231-2, 08-2251-0, 08-2301-3,08-2351-8,08-3201-4,08-3231-1,08-3251-9,08-3301-2,08-4123-1, 08-4223-7, 08-4225-1' 08-4230-2, 08-4231-0, 08-
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1872-2012·2012-07-04

    Colgate 360 Toothbrush Recalled Due to Battery Cap Defect

    Colgate-Palmolive is recalling 280,044 Colgate 360 battery-powered toothbrushes because the battery cap may blow off the handle.

    Product
    Colgate 360 Replaceable Head Battery Powered Toothbrush Medium UPC03500068750 Dist. by Colgate-Palmolive Co. New York, NY 10022 Made in China. For teeth cleansing.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1896-2012·2012-07-04

    Philips HeartStart MRx Monitor/Defibrillators Recalled for ECG Failure

    Philips is recalling HeartStart MRx monitor/defibrillators because they may fail to display ECG signals, potentially delaying the treatment of cardiac arrhythmias.

    Product
    Philips HeartStart MRx monitor/defibrillators Models: M3535A, M3536A, M3536M4, M3536M5, and M3536M6 Product Usage: The Heartstart MRx is for use for the termination of ventricular tachycardia and ventricular fibrillation. The device is for use by qualified medical personnel
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1886-2012·2012-07-04

    Terumo Recalls Sarns Antegrade Cardioplegia Cannulas Due to Foreign Substance

    Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannulas because a foreign substance was found on the inner surface of some tips that could be dislodged.

    Product
    X-COATED FX25RW H/L PACK Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during card
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1890-2012·2012-07-04

    Terumo Recalls Sarns Antegrade Cardioplegia Cannula Kits Due to Foreign Substance

    Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannula kits because a foreign substance was found on the inner surface of some cannula tips that could be dislodged.

    Product
    CPB CATHETER KIT- DR OWEN Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during car
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1888-2012·2012-07-04

    Terumo Recalls Sarns Antegrade Cardioplegia Cannula Due to Foreign Substance

    Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannulae because a foreign substance was found on the inner surface of some tips that could be dislodged.

    Product
    CUSTOM CPB CATHETER KIT-DR. Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during c
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1866-2012·2012-07-04

    Stryker Endoscopy Recalls Formula Shaver Handpieces Due to Routine Check Concerns

    Stryker Endoscopy is recalling 34 Formula and Formula 180 Shaver Handpieces because routine checks to ensure accuracy and fitness for use may not have been adequately determined.

    Product
    Formula Shaver Handpiece (with buttons); Formula 180 Shaver Handpiece (with button) Rx only, Made USA.: Stryker Endoscopy 5900 Optical Court San Jose, CA 95138 Components within the Crossfire System that provided abrasion, resection, debridement and removal of bone and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1892-2012·2012-07-04

    Terumo Recalls Sarns Cardioplegia Cannula Kits Due to Foreign Substance

    Terumo is recalling Sarns Antegrade Cardioplegia Cannula kits because a foreign substance was found on the inner surface of some tips that could dislodge.

    Product
    CPB CATHETER KIT-DR VANTRIGHT Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1876-2012·2012-07-04

    Terumo Recalls Sarns Antegrade Cardioplegia Cannulas Due to Foreign Substance

    Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannulas because a foreign substance was found on the inner surface of some tips that can be dislodged.

    Product
    SARNS ANTEGRADE: CARDIOPLEGIA CANNULA: ROOT INFUSION VENT/CATHETER WITH 14- GAUGE WHITE NEEDLE, RECTANGULAR FLANGE, 6" (15 CM) LONG Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardiopl
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1873-2012·2012-07-04

    Colgate 360 Toothbrush Recalled Due to Battery Cap Defect

    Colgate-Palmolive is recalling 280,044 units of Colgate 360 battery-powered toothbrushes because the battery cap may blow off the handle.

    Product
    Colgate 360 Replaceable Head Battery Powered Toothbrush Soft UPC 03500068747 Dist. by Colgate-Palmolive Co. New York, NY 10022 Made in China. For teeth cleansing.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1870-2012·2012-07-04

    Colgate Adult Motion Battery Toothbrush Recalled for Battery Cap Defect

    Colgate-Palmolive is recalling 6,006 Adult Motion Battery Toothbrushes because the battery cap may blow off the handle.

    Product
    Colgate Adult Motion Battery Toothbrush UPC 035000686213 Dist. by Colgate-Palmolive Co. New York, NY 10022 Made in China. For teeth cleansing.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1861-2012·2012-07-04

    Stryker Rose Bed Recall Due to Loadcell Failure in Scale Function

    Stryker is recalling Rose Model FL14E beds because loadcell failures cause scale errors and disabled bed exit functions.

    Product
    Stryker Rose Bed Model (FL14E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface co
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1889-2012·2012-07-04

    Terumo Recalls Sarns Cardioplegia Cannula Kits Due to Foreign Substance

    Terumo is recalling Sarns Cardioplegia Cannula Kits because a foreign substance was found on the inner surface of some cannula tips that could be dislodged.

    Product
    CPB CATHETER KIT-DR GERHARDT Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1670-2012·2012-07-04

    Smart Juice Organic Pomegranate Juice Recalled for Lead Contamination

    Smart Juice LLC is recalling Organic 100% Pomegranate Juice due to lead levels above allowable limits. Consumers in 12 states should stop using the product.

    Product
    Organic 100% Pomegranate Juice packed in glass bottles Smart Juice Organic Pomegranate 100% Juice 33.8 FL. Oz. 100% Juice Distributed by: Smart Juices LLC, Bethlehem, PA 18018 BBE: 09.09.2014 ORGANIC N49
    Category
    Food
    Distribution
    12 states
  • HighFDA (Food)·F-1642-2012·2012-07-04

    Bay Valley Foods Recalls Pasta Mixes Due to Metal Fragments

    Bay Valley Foods is voluntarily recalling approximately 74,000 cases of boxed pasta mix products because they contain a seasoning blend that may have small metal fragments.

    Product
    Reggano, Linguine and Parmesan Pasta Entree, NET WT 4.8 OZ(136g), UPC 4149813345, Distributed by ALDI Inc., Batavia, IL 60510.
    Category
    Food
    Distribution
    25 states
  • HighFDA (Food)·F-1675-2012·2012-07-04

    Crispy Almond Cake Rusk Recalled for Undeclared Milk

    Indian Foods & Spices, LLC is recalling Crispy by TWI Foods Almond Cake Rusk because the product may contain undeclared milk.

    Product
    Crispy by TWI Foods Almond Cake Rusk, Biscotte Croustillante Almande, Net Wt 750 g, Product of Canada Manufactured by TWI Foods Inc. 1869 Gage Court, Mississauga, Ont, Canada L5S 1S3.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1678-2012·2012-07-04

    TWI Foods Coconut Cookies Recalled for Undeclared Milk

    Indian Foods & Spices, LLC is recalling 54 units of Crispy TWI Foods Coconut Cookies because the product may contain undeclared milk.

    Product
    Crispy TWI Foods Coconut Cookies, Biscuit, Net Wt 400 g, Product of Canada Manufactured by TWI Foods Inc. 1869 Gage Court, Mississauga, Ont, Canada L5S 1S3.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1645-2012·2012-07-04

    Bay Valley Foods Recalls Pasta Salad Mix Due to Metal Fragments

    Bay Valley Foods is voluntarily recalling approximately 74,000 cases of boxed pasta mix products because they may contain small metal fragments.

    Product
    Food Club Pasta Salad Classics Ranch & Bacon, NET WT 7.5 OZ ( 212g), UPC 3680034311, Distributed by TOPCO ASSOCIATED, LLC, 7711 GROSS POINT ROAD, SKOKIE, IL 60077
    Category
    Food
    Distribution
    25 states
  • HighFDA (Food)·F-1647-2012·2012-07-04

    Bay Valley Foods Recalls Macaroni and Cheese for Metal Fragments

    Bay Valley Foods is voluntarily recalling Kroger Macaroni & Cheese products because they contain a seasoning blend that may have small metal fragments.

    Product
    Kroger, Macaroni & Cheese Rich n Creamy, NET WT 7.25 OZ (205 g), UPC 1111085149, DISTRIBUTED BY KROGER CO, CINCINNATI, OH 45202.
    Category
    Food
    Distribution
    25 states
  • HighFDA (Food)·F-1643-2012·2012-07-04

    Bay Valley Foods Recalls Pasta Mix Due to Metal Fragments

    Bay Valley Foods is voluntarily recalling boxed pasta mix products because a seasoning blend may contain small metal fragments.

    Product
    Reggano Pasta Salad Classic, UPC 4149812863, Distributed by ALDI Inc., Batavia, IL 60510.
    Category
    Food
    Distribution
    25 states
  • HighFDA (Devices)·Z-1879-2012·2012-07-04

    Terumo Recalls Sarns Cardioplegia Cannulas Due to Foreign Substance

    Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannulas because a foreign substance on the inner surface may dislodge during use.

    Product
    FX PACK Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during cardiopulmonary bypas
    Category
    Medical Device
    Distribution
    Distributed nationwide

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