The Recall Desk

Archive

May 2015 recalls

653 recalls were announced in May 2015.

What the numbers show

Critical
52
Severe
166
High
331
Moderate
90
Low
14

Of the 653 recalls this month scored against our rubric, 8% are Critical, 25% are Severe.

301–400 of 653

  • LowFDA (Devices)·Z-1596-2015·2015-05-20

    Arc Medical Recalls ThermoFlo 1 HME Due to Incorrect Outer Carton Expiry Date

    Arc Medical Inc is recalling 1,810 units of ThermoFlo 1 HME because the outer shipping carton displayed an incorrect expiry date, although the inner product carton was labeled correctly.

    Product
    ThermoFlo 1 HME, Disposable, Non-sterile, Expiry date 04/17. Used as a humidifier in a breathing circuit.
    Category
    Medical Device
    Distribution
    2 states
  • LowFDA (Devices)·Z-1597-2015·2015-05-20

    Spinal Elements Mercury Lordosed Rods Recalled for Missing Traceability Markings

    Spinal Elements, Inc. is recalling 588 Mercury lordosed rods because some lack required product identification markings, interrupting device traceability.

    Product
    Spinal Elements 5.5 x 45MM Mercury lordosed rod. A component of the Mercury Spinal System, comprised of a variety of screws, hooks, rods, connectors, and staples that are used for attachment to the non-cervical spine. Rods span the distance between screws and hooks and achieve…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1077-2015·2015-05-20

    FDA Recalls Monistat 1 Simple Cure for Missing Topical Cream

    Medtech Products, Inc. is recalling Monistat 1 Simple Cure because the distributed units lack the required topical cream.

    Product
    MONISTAT 1 COMBINATION PACK — MONISTAT 1 COMBINATION PACK (MICONAZOLE NITRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1079-2015·2015-05-20

    Apotex Recalls Subpotent Olanzapine Orally Disintegrating Tablets

    Apotex Inc. is voluntarily recalling specific lots of Olanzapine 5 mg orally disintegrating tablets because they contain less active drug than labeled.

    Product
    Olanzapine, Orally Disintegrating Tablets, 5 mg, a) 30-count bottle (NDC 60505-3275-03), b) 100-count blister (NDC 60505-3275-00), Rx only, Manufactured by Apotex Inc. Toronto, Ontario Canada, M9L 1T9
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1081-2015·2015-05-20

    Apotex Recalls Subpotent Olanzapine Orally Disintegrating Tablets

    Apotex Inc. is voluntarily recalling 5,352 bottles of Olanzapine 20 mg tablets because the drug was found to be subpotent.

    Product
    Olanzapine, Orally Disintegrating Tablets, 20 mg, 30-count bottle, Rx only, Manufactured by Apotex Inc. Toronto, Ontario Canada, M9L 1T9
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V294000·2015-05-19

    Blue Bird All American Buses Recalled for Engine Fire Risk

    Blue Bird is recalling 2009-2016 All American non-school buses due to a defect that may allow engine oil to contact hot surfaces, increasing fire risk.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V296000·2015-05-19

    NABI Transit Bus Recall for Engine Vent Tube Fire Risk

    NABI is recalling 2007-2015 LFW, BRT, and 2007-2013 CLFW transit buses because a vent tube may detach, allowing engine oil to contact hot surfaces and cause a fire.

    Product
    NABI — NABI CLFW, LFW, BRT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15138·2015-05-19

    Precision Trading Recalls Espresso Makers Due to Burn Risk

    Precision Trading is recalling about 4,700 PREMIUM Espresso Makers because the filler cap can crack or pop off, releasing steam and posing a burn risk.

    Product
    PREMIUM® Espresso Makers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15139·2015-05-19

    Kaldi's Coffee Recalls Disposable Cup Sleeves Due to Fire Hazard

    Kaldi's Coffee Roasting is recalling about 700,000 disposable paper cup sleeves because they can ignite in microwaves. Two fire incidents were reported, with no injuries.

    Product
    Disposable Cup Sleeves
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V295000·2015-05-19

    Gillig Low Floor Bus Taillight Bracket Recall

    Gillig is recalling 2014-2015 Low Floor buses because taillight brackets may detach, reducing visibility and increasing crash risk.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·15E040000·2015-05-18

    Takata Frontal Driver Air Bag Inflator Module Recall

    Takata is recalling specific frontal driver air bag inflator modules that may rupture during deployment, potentially causing serious injury or death.

    Product
    AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E042000·2015-05-18

    Takata Passenger Air Bag Inflator Recall for Honda, Toyota, Pontiac, Subaru

    Takata is recalling PSPI-L passenger air bag inflators in specific Honda, Toyota, Pontiac, and Subaru models. The inflators may rupture in a crash, sending metal fragments into the vehicle.

    Product
    AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V290000·2015-05-18

    RAM 4500 and 5500 Trucks Recalled for Tire Speed Rating Mismatch

    Chrysler is recalling 2014-2015 RAM 4500 and 5500 trucks because their tires are rated for a lower speed than the vehicle's maximum capability, posing a crash risk.

    Product
    RAM — RAM 4500, 5500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·080-2015·2015-05-18

    ZYK Enterprises Recalls Boneless Veal Trim for E. Coli O157:H7 Contamination

    ZYK Enterprises is recalling 2,522 pounds of boneless veal trim and whole muscle cuts due to possible E. coli O157:H7 contamination. The products were distributed to wholesale establishments in California, Massachusetts, and Washington.

    Product
    ZYK Enterprises, Inc. — ZYK Enterprises, Inc. Recalls Boneless Veal Trim Products Due to Possible Contamination with E. Coli O157:H7
    Category
    Food
    Distribution
    3 states
  • SevereNHTSA·15E041000·2015-05-18

    Takata Passenger Air Bag Inflator Recall for 2001-2008 Vehicles

    Takata is recalling specific passenger frontal air bag inflators for 2001-2008 vehicles due to a risk of rupture during deployment.

    Product
    AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V292000·2015-05-18

    New Flyer Buses Recalled for Engine Vent Tube Fire Risk

    New Flyer is recalling certain 2008-2014 buses because a vent tube may detach, allowing engine oil to contact hot surfaces and increase fire risk.

    Product
    NEW FLYER — NEW FLYER C40LF, C40LFR, C35LF, C35LFR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V291000·2015-05-18

    Fiat 500 Electric Recall for Transmission Shifting to Neutral

    Chrysler is recalling 2013-2015 Fiat 500 electric vehicles because a software issue may cause the transmission to unexpectedly shift to neutral, increasing crash risk.

    Product
    FIAT — FIAT 500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·078-2015·2015-05-16

    A.S.K. Foods Recalls Herb Stuffing Due to Undeclared Soy Allergen

    A.S.K. Foods is recalling 414 pounds of Wegmans Herb Stuffing with Pork and Veal because the product contains undeclared soy lecithin.

    Product
    A.S.K. Foods Inc. — A.S.K. Foods, Inc. Recalls Herb Stuffing with Pork and Veal Product Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·15V288000·2015-05-15

    Daimler Orion VII Buses Recalled for Engine Fire Risk

    Daimler Buses North America is recalling 2007-2012 Orion VII natural gas buses because engine oil may contact hot surfaces, increasing fire risk.

    Product
    ORION — ORION VII
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V287000·2015-05-15

    Nissan Recalls Vehicles Due to Passenger Air Bag Inflator Rupture Risk

    Nissan is recalling specific 2001-2006 models because the passenger air bag inflator may rupture during deployment, potentially sending metal fragments into the vehicle.

    Product
    NISSAN — NISSAN, INFINITI PATHFINDER, FX35, I30, FX45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E039000·2015-05-15

    Industrial Axle Company Recalls ALKO AXIS Trailer Axle Hubs

    Industrial Axle Company is recalling specific ALKO AXIS trailer axles because wheel mounting studs may fail, potentially causing wheel separation and increasing crash risk.

    Product
    SUSPENSION:REAR:AXLE:NON-POWERED AXLE ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·079-2015·2015-05-14

    AA Poultry Recalls Chicken and Turkey Due to Unapproved Substance

    AA Poultry Processing is recalling chicken and turkey products contaminated with trichloro-s-triazinetrione, an unapproved substance.

    Product
    Pine Creek Processing LLC — AA Poultry Processing, LLC Recalls Chicken and Turkey Products Due to Use of Unapproved Substance
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0982-2015·2015-05-13

    Physician Preferred Medical Recalls Epel 18 mg Estradiol Pellets Due to Sterility Failure

    Physician Preferred Medical, LLC is recalling Epel 18 mg Estradiol Pellets because the specific lot failed sterility testing. The product was distributed in Arizona and Kansas.

    Product
    Epel 18 mg Estradiol Pellet, For In Office Use Only, For In Office Administration Only, Not for Resale or Dispensing to an Individual Patient, Rx Only, Preferred Physician Medical LLC, 405-551-8216
    Category
    Drug
    Distribution
    2 states
  • CriticalFDA (Food)·F-2196-2015·2015-05-13

    La Terra Fina Spinach Artichoke Dip Recalled for Listeria Risk

    La Terra Fina is recalling specific lots of Chunky Spinach Artichoke & Parmesan Dip because the chopped spinach ingredient tested positive for Listeria monocytogenes.

    Product
    La Terra Fina Chunky Spinach Artichoke & Parmesan Dip 31-ounce tub Keep refrigerated 31-ounce tub; UPC: 6-40410-51193-4 Item number 407600 - Costco Item number 4300193 - Smart and Final 10 oz. Retail size - UPC 6-40410-51327-3 Manufactured by La Terra Fina, Union…
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Drugs)·D-0977-2015·2015-05-13

    FDA Recalls EDGE Weight Release Capsules Containing Unapproved Drugs

    Detox Transforms is recalling EDGE Amplified Weight Release capsules because the product contains undeclared phenolphthalein and fluoxetine, making it an unapproved drug.

    Product
    EDGE Amplified Weight Release capsules, 400 mg, 60-count bottle, Developed by Signature, 1027 Highway 70 W, Suite 227, Garner, NC 27529, UPC 8 52175 00417 4.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0991-2015·2015-05-13

    Ultra ZX Dietary Supplement Recalled for Undeclared Sibutramine and Phenolphthalein

    Ultra ZX Labs is recalling Ultra ZX dietary supplements because FDA testing found undeclared sibutramine and phenolphthalein. The product was marketed without an approved NDA or ANDA.

    Product
    ULTRA ZX DIETARY SUPPLEMENT (Extracto de Naranjo Amargo 70, Extracto de semilla de Sen 47.6, Lagrima de Coix 42, Almidon Medico 84), 30 capsule bottles, Manufactured and distributed by: Ultra ZX Labs, L.L.C. 2525 SW 3rd Ave Apt 1704 Miami, Florida 33129-2068.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0981-2015·2015-05-13

    FDA Recalls iNSANE Bee Pollen Capsules Containing Unapproved Drugs

    The FDA is recalling iNSANE Bee Pollen capsules because they contain undeclared phenolphthalein and fluoxetine, making them unapproved drugs.

    Product
    iNSANE Bee Pollen capsules, 200 mg, 60-count bottle, Developed by Signature, 1027 Highway 70 W, Suite 227, Garner, NC 27529, UPC 8 52175 00408 2.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0994-2015·2015-05-13

    Forever Beautiful Bee Pollen Recalled for Contaminants

    REFA Enterprises is recalling Forever Beautiful Bee Pollen capsules because FDA analysis found the product contains sibutramine and phenolphthalein.

    Product
    Forever Beautiful BEE POLLEN, capsules, 250mg in 60-count bottles, 900 Commonwealth Place, Ste 104, Virginia Beach, VA
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0993-2015·2015-05-13

    REFA Enterprises Recalls Forever Beautiful INFINITY Capsules for Unapproved Ingredients

    REFA Enterprises is recalling Forever Beautiful INFINITY capsules because FDA analysis found the product contains sibutramine and phenolphthalein without an approved NDA/ANDA.

    Product
    Forever Beautiful INFINITY, capsules, 300mg in 60-count bottles, 900 Commonwealth Place, Ste 104, Virginia Beach, VA
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0988-2015·2015-05-13

    FDA Recalls Estrastain Pro-Anabolic Mass and Hardening Complex Capsules

    Anabolic Science Labs LLC is recalling Estrastain Pro-Anabolic Mass and Hardening Complex capsules because they contain unapproved synthetic hormone ingredients.

    Product
    ESTRASTAIN PRO-ANABOLIC MASS AND HARDENING COMPLEX (Estra-4,9,11-triene-3,17-dione 15mg, 2a-3a-epithio-17a-methyl-5a-androstan-17b-ol 10 mg), Capsules, 60 count bottle, Manufactured for: Wyked Labs LLC, Winter Park, FL 32789
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2194-2015·2015-05-13

    La Terra Fina Spinach Dip Recalled for Listeria Contamination

    La Terra Fina is recalling Organic Thick & Creamy Spinach Dip and Spread because the chopped spinach ingredient tested positive for Listeria monocytogenes.

    Product
    La Terra Fina Organic Thick & Creamy Spinach Dip and Spread; Made with Greek Yogurt. 24 oz. plastic tub (1 lb. 8 oz,) 680 g: Keep refrigerated UPC 640410513730. Manufactured by" La Terra Fina, Union City, CA 94587
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Drugs)·D-0989-2015·2015-05-13

    FDA Recalls Unapproved Anabolic Steroid Supplements from Anabolic Science Labs

    Anabolic Science Labs is recalling SWOLL-250 Super Mass Builder Quad Stack capsules because they contain unapproved synthetic hormone ingredients.

    Product
    SWOLL-250 SUPER MASS BUILDER QUAD STACK (18-Methylestr-4-en-3-one-17b-ol 15mg, 6-a-Chloro-androst-4-en-17b-ol-3-one 15mg, 13-ethyl-3-methoxy-gona-2,5(10)-diene-17-one 15mg, 2,17a-dimethyl-5a-androsta-1-en-17b-ol-3-one 3 mg), Capsules, 90 count bottle, Manufactured for: Wyked…
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2153-2015·2015-05-13

    Spiceco Recalls Hungarian Paprika Due to Undeclared Peanut Protein

    Spiceco is recalling Pride of Szeged Sweet Hungarian Paprika because it may contain undeclared peanut protein. The recall includes additional products containing the implicated paprika.

    Product
    Pride of Szeged Hungarian Exquisite 100 % Sweet Delicacy Paprika, Net Wt. 5 oz., 142g, UPC 0 78006 00010 2
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0979-2015·2015-05-13

    AMPD GOLD Bee Pollen Recalled for Undeclared Sildenafil

    Detox Transforms is recalling AMPD GOLD Bee Pollen capsules because they contain undeclared sildenafil, making them unapproved drugs.

    Product
    AMPD GOLD Bee Pollen capsules, 350 mg, 60-count bottle, Signature, 1027 Highway 70 W, Suite 227, Garner, NC 27529, UPC 8 52175 00418 1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0986-2015·2015-05-13

    FDA Recalls Unapproved Anabolic Steroid Product HALO-70 MEGA MASS BUILDER

    The FDA is recalling HALO-70 MEGA MASS BUILDER capsules because they contain an unapproved synthetic hormone ingredient, making them unapproved new drugs.

    Product
    HALO-70 MEGA MASS BUILDER (4-chloro-17a-methyl-androst-1,4-diene-3b,17b-diol 35mg), Capsules, 60 count bottle, Manufactured for: Wyked Labs LLC, Winter Park, FL 32789
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0978-2015·2015-05-13

    Detox Transforms Recalls iNDiGO Capsules Containing Undeclared Phenolphthalein

    Detox Transforms is recalling iNDiGO capsules because they contain undeclared phenolphthalein, making the product an unapproved drug.

    Product
    iNDiGO capsules, 220 mg, 60-count bottle, Developed by Signature, 1027 Highway 70 W, Suite 227, Garner, NC 27529, UPC 8 52175 00404 4.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V286000·2015-05-13

    Toyota Recalls Vehicles for Front Passenger Air Bag Inflator Rupture Risk

    Toyota is recalling specific 2002-2007 Lexus, Toyota, and Pontiac vehicles because the front passenger air bag inflator may rupture during a crash, potentially causing serious injury or death.

    Product
    PONTIAC — PONTIAC, LEXUS, TOYOTA VIBE, SC, SEQUOIA, TUNDRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0985-2015·2015-05-13

    FDA Recalls M14-Ment Advanced Mass Builder for Unapproved Steroid Ingredient

    The FDA is recalling M14-Ment Advanced Mass Builder capsules because they contain an unapproved synthetic hormone ingredient, making them unapproved new drugs.

    Product
    M14-MENT ADVANCED MASS BUILDER (7a-Methyl-estra-4-en-3,17-dione MENT 5mg, M14D 20 mg), Capsules, 90 count bottle, Manufactured for: Wyked Labs LLC, Winter Park, FL 32789
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2147-2015·2015-05-13

    Royal Frozen Food Recalls Blintzes with Cherry Due to Undeclared Milk

    Royal Frozen Food is recalling Blintzes with Cherry because the product contains undeclared milk. The recall affects 3,600 units distributed in California and Nevada.

    Product
    Blintzes with Cherry, Net Wt. 18oz (510g), 10 pieces. 18-oz. plastic trays containing ten pieces of Royal Frozen Food, BLINTZES Blintzes with Cherry with bar code 6 0723830021 8; 12 packs per case.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0976-2015·2015-05-13

    Hospira Recalls 0.9% Sodium Chloride Injection Due to Human Hair

    Hospira Inc. is recalling 9,912 units of 0.9% Sodium Chloride Injection, USP, 250 mL, because human hair was found floating in the IV solution.

    Product
    0.9% Sodium Chloride Injection, USP, 250 mL, Rx only, VisIV Container, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-25.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2148-2015·2015-05-13

    Royal Frozen Food Recalls Blintzes with Potato for Undeclared Milk

    Royal Frozen Food is recalling Blintzes with Potato because they contain undeclared milk. The recall affects 3,600 units distributed in California and Nevada.

    Product
    Blintzes with Potato, Net Wt. 18oz (510g), 10 pieces. 18-oz. plastic trays containing ten pieces of Royal Frozen Food, BLINTZES Blintzes with Potato with bar code 6 0723830020 1; 12 packs per case.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-2169-2015·2015-05-13

    International Foodsource Recalls Ground Cumin Due to Peanut Protein

    International Foodsource, LLC is recalling ground cumin that may contain peanut protein. The product was distributed in Illinois, Massachusetts, Maryland, and Virginia.

    Product
    Ground Cumin, Bulk Package Size: a) 50 lb. paper carton b) 16 oz. jar/ 8 plastic jars per case
    Category
    Food
    Distribution
    4 states
  • SevereNHTSA·15V283000·2015-05-13

    Forest River Recalls 2014-2015 Glaval Transit Buses for Loose Tie Rod Nut

    Forest River is recalling 226 model year 2014-2015 Glaval transit buses because a loose tie rod jam nut may cause loss of control.

    Product
    GLAVAL BUS — GLAVAL BUS UNIVERSAL, LEGACY, TITAN II, TITAN II LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V284000·2015-05-13

    Toyota Recalls 2004-2005 RAV4 Vehicles Due to Air Bag Defect

    Toyota is recalling 2004-2005 RAV4 vehicles because the driver's air bag inflator may rupture during deployment, posing a risk of serious injury or death.

    Product
    TOYOTA — TOYOTA RAV4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2195-2015·2015-05-13

    La Terra Fina Spinach Artichoke Dip Recalled for Listeria Risk

    La Terra Fina is recalling Spinach Artichoke & Parmesan Dip made with Greek Yogurt because a supplier notified the firm that the product contained IQF chopped spinach that tested positive for Listeria Monocytogenes.

    Product
    La Terra Fina Spinach Artichoke & Parmesan Dip made with Greek Yogurt 31-ounce tub Keep refrigerated UPC 6-40410-51338-9 Manufactured by" La Terra Fina, Union City, CA 94587
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-2151-2015·2015-05-13

    Wawa Kale and Quinoa Salad Recalled for Undeclared Soy Allergen

    Taylor Farms Florida is recalling Wawa brand Kale and Quinoa Salad because the packaging fails to declare soy as an ingredient.

    Product
    Wawa brand Kale and Quinoa Salad, 7.5-oz. plastic container, UPC Code: 726191066402
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-2145-2015·2015-05-13

    Ossie's Pickled Lox Recalled for Undeclared Milk Allergen

    SM Fish Corp is recalling Ossie's Pickled Lox Dairy due to undeclared milk. The product was distributed in New York and New Jersey.

    Product
    OSSIE'S PICKLED LOX DAIRY, NET WT. 8 OZ, UPC 739885114136 --- The product is packaged in clear, plastic containers/tubs.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-2173-2015·2015-05-13

    Giant Eagle Store-Cut Fontal Cheese Recalled for Undeclared Egg Allergen

    Giant Eagle is recalling store-cut Fontal cheese because it contains lysozyme, an egg allergen, that was not declared on the label.

    Product
    Giant Eagle Store cut Fontal Cheese wrapped in plastic wrap Belgium Imported Fontal - CD; Sell By: (up to and including) 04/23/2015 PLU: 16124 Giant Eagle Distributed by: Giant Eagle, Inc., Pittsburgh, PA 15238
    Category
    Food
    Distribution
    0 states
  • SevereNHTSA·15V281000·2015-05-13

    Autocar Recalls Xpert and XSpotter Vehicles for Engine Fire Risk

    Autocar is recalling 2014-2016 Xpert and XSpotter vehicles because a vent tube defect may allow engine oil to contact hot surfaces, increasing fire risk.

    Product
    AUTOCAR — AUTOCAR XSPOTTER, XPERT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2150-2015·2015-05-13

    Deer Brand Golden Raisins Recalled for Undeclared Sulfites

    Best Foods NJ, Inc. is recalling Deer Brand Golden Raisins because they contain undeclared sulfites, a potential allergen.

    Product
    Deer Raisin Golden 7 oz., marked and unmarked packages Packed for Best Foods Inc. Edison, NJ 08817 Some have UPC 714760029255. packaged in clear plastic packages.
    Category
    Food
    Distribution
    8 states
  • SevereNHTSA·15V285000·2015-05-13

    Toyota Recalls Vehicles for Defective Passenger Air Bag Inflators

    Toyota is recalling approximately 1.97 million vehicles, including Pontiac, Lexus, and Toyota models, to replace passenger air bag inflators that may rupture.

    Product
    TOYOTA — TOYOTA, PONTIAC, LEXUS COROLLA MATRIX, VIBE, SC, SEQUOIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V280000·2015-05-13

    Autocar Recalls Xpeditor Vehicles Due to Engine Fire Risk

    Autocar is recalling 2008-2016 Xpeditor vehicles because a vent tube may detach, allowing engine oil to contact hot surfaces and increase the risk of a vehicle fire.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2149-2015·2015-05-13

    Royal Frozen Food Recalls Blintzes with Potato and Mushroom Due to Undeclared Milk

    Royal Frozen Food is recalling Blintzes with Potato & Mushroom because they contain undeclared milk. The recall affects 3,600 units distributed in California and Nevada.

    Product
    Blintzes with Potato & Mushroom, Net. Wt. 18oz (510g), 10 pieces. 18-oz. plastic trays containing ten pieces of Royal Frozen Food, BLINTZES Blintzes with Potato Mushroom with bar code 6 0723830020 1. 12 packs per case.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-2146-2015·2015-05-13

    Ossie's Pickled Lox Recalled for Undeclared Egg Allergen

    SM Fish Corp is recalling Ossie's Pickled Lox & Cream because it contains undeclared eggs, a sub-ingredient of the mayonnaise.

    Product
    OSSIE'S PICKLED LOX & CREAM, NET WT. 8 OZ, UPC 739885114136 --- The product is packaged in clear, plastic containers/tubs.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0984-2015·2015-05-13

    FDA Recalls M1-Alpha Labs Mega Mass Builder for Unapproved Steroid Ingredient

    The FDA is recalling M1-Alpha Labs Mega Mass Builder capsules because they contain an unapproved synthetic hormone ingredient, making them unapproved new drugs.

    Product
    M1-ALPHA LABS MEGA MASS BUILDER (M1A, Methyl-1-Etiocholenolol- 20mg, Epietiocholanolone) Capsules, 60 count bottle, Manufactured for: Wyked Labs LLC, Winter Park, FL 32789
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0987-2015·2015-05-13

    FDA Recalls 7-Ment Alpha Advanced Mass Builder for Unapproved Steroid Ingredient

    The FDA is recalling 7-Ment Alpha Advanced Mass Builder capsules because they contain an unapproved synthetic hormone ingredient.

    Product
    7-MENT ALPHA ADVANCED MASS BUILDER (7a-methyl-estra-4-en-3,17-dione 10 mg), Capsules, 90 count bottle, Manufactured for: Wyked Labs LLC, Winter Park, FL 32789
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0980-2015·2015-05-13

    BtRiM Max capsules recalled for undeclared phenolphthalein

    Detox Transforms is recalling BtRiM Max capsules because they contain undeclared phenolphthalein, making the product an unapproved drug.

    Product
    BtRiM Max capsules, 60-count bottle, Developed by Signature, 1027 Highway 70 W, Suite 227, Garner, NC 27529, UPC 8 52175 00406 8.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2144-2015·2015-05-13

    SM Fish Corp Recalls Ossie's Herring in Sour Cream for Undeclared Milk

    SM Fish Corp is recalling 266 units of Ossie's Herring in Sour Cream due to undeclared milk. The product was distributed in New York and New Jersey.

    Product
    OSSIE'S HERRING IN SOURCREAM, NET WT. 8 OZ, UPC 739885114174 --- The product is packaged in clear, plastic containers/tubs.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0990-2015·2015-05-13

    FDA Recalls Professional Formexx Black Due to Unapproved Steroid Ingredient

    Anabolic Science Labs is recalling Professional Formexx Black capsules because they contain an unapproved synthetic hormone ingredient.

    Product
    PROFESSIONAL FORMEXX BLACK (AromaMaXX 250mg: 13-dimethyl-1,2,7,8,9,11,12,14,15,16-decahydro-cyclopenta[a]phenanthrene-3,6,17-trione,4-Androsten 4,17-beta-diol-3one), Capsules, 60 count bottle, Manufactured for: ANABOLIC SCIENCE LABS WINTER PARK, FL 32789
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1574-2015·2015-05-13

    MHI-TM2000 Linear Accelerator System Software Recall for Communication Errors

    Mitsubishi Heavy Industries is recalling 11 MHI-TM2000 Linear Accelerator Systems due to a software defect that allows radiation delivery despite communication errors and prevents saving treatment records.

    Product
    MHI-TM2000 Linear Accelerator System (Software Version 3.5.0 and 3.5.1)
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-1586-2015·2015-05-13

    Bard MAX-CORE Biopsy Instruments Recalled for Self-Activation Risk

    Bard Peripheral Vascular Inc is recalling 7,995 Bard MAX-CORE Disposable Core Biopsy Instruments due to a risk of self-activation-related issues.

    Product
    BARD MAX-CORE Disposable Core Biopsy Instrument Gauge x Length 18g x 20cm The BARD MAX-CORE Disposable Core Biopsy Instrument is a single patient use core biopsy device. It is available in several needle gauge sizes and lengths. The side and rear actuator buttons are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2155-2015·2015-05-13

    Spiceco Recalls Emeril's Blackened Seasoning Blend for Undeclared Peanut

    Spiceco is recalling Emeril's Blackened Seasoning Blend because it may contain undeclared peanut protein. The recall includes 2,483 cases distributed nationwide and abroad.

    Product
    Emeril's Blackened Seasoning Blend, 3.1 oz. (88g) Distributed by: B&G Foods, Inc., Parsippany, NJ 07054 USA, UPC 074683097633
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1577-2015·2015-05-13

    Spacelabs Ultraview SL Command Modules Recalled for Random Resets

    Spacelabs is recalling Ultraview SL Command Modules with specific Masimo SpO2 components due to a defect causing random resets.

    Product
    Ultraview SL Command Modules, Model 91496, with the Masimo SpO2 PCBA, PN: 010-1636-02. The Spacelabs Multi-parameter Module is intended for use with the Patient Care Management System (PCMS) to acquire, monitor, and process various clinical parameters from an adult or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1573-2015·2015-05-13

    Stryker Recalls Ambulating Bulbs Due to Potential Sterility Breach

    Stryker Instruments is voluntarily recalling Ambulating Bulbs used with wound drains because of a potential sterility breach in the packaging.

    Product
    Ambulating Bulb Ambulating Bulb: The Ambulating Bulb comprises four main components: the suction reservoir, the PVC tubing, the slide clamp and the female connector. The rigid polycarbonate female connector is used to connect the ambulating bulb to the CBCII evacuator tube in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2193-2015·2015-05-13

    Whole Foods Market Rye Bread Recalled for Undeclared Wheat

    Whole Foods Market is recalling Health Starts Here Rye Bread in Texas, Oklahoma, Arkansas, and Louisiana due to undeclared wheat.

    Product
    Whole Foods Market Health Starts Here Rye Bread (formerly 100% Rye) 16 oz. PLU# 41844
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-1593-2015·2015-05-13

    ICU Medical Recalls MicroClave T-Connectors Due to Potential Leakage

    ICU Medical is recalling 5,100 units of MicroClave T-Connectors because potential connection separation issues could lead to leakage.

    Product
    127" (323cm) Transfer Set w/Check Valve, MicroClave T-Connector, Anti-Siphon Valve, Clamp, Luer Lock, Non-DEHP Tubing, Item No. B33351 Product Usage: IV Administration sets are intended for the infusion and withdrawal of fluids. The devices are provided sterile.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2175-2015·2015-05-13

    Cott Beverages Recalls Red Rain Energy Drink for Unlabeled Tree Nuts

    Cott Beverages is recalling Red Rain Energy Drink Tropical Mango because it may contain trace amounts of walnuts, a tree nut not listed on the ingredient label.

    Product
    Red Rain Energy Drink Tropical Mango
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-2166-2015·2015-05-13

    Spiceco Recalls Fish Rub Seasoning for Undeclared Peanut Protein

    Spiceco is recalling Pride of Szeged Fish Rub Seasoning because it may contain undeclared peanut protein. The recall includes additional products using the implicated paprika.

    Product
    Pride of Szeged Fish Rub Seasoning Net Wt. 5 oz (142 g) Spiceco, Avenel NJ 07001 UPC 078006020018 2.75 oz 50 lb boxes
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2156-2015·2015-05-13

    Spiceco Recalls Sylvia's Rib Rub N More Seasoning for Undeclared Peanut

    Spiceco, Inc. is recalling Sylvia's Rib Rub N More Seasoning because it may contain undeclared peanut protein. The recall includes 324 cases distributed nationwide and abroad.

    Product
    Sylvia's Rib Rub N More Seasoning, Net Wt. 5.5 oz. (155g), Distributed by: Sylvia Woods Food Company, P.O. Box 240, Harlem, NY 10027, UPC 608623000683
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1460-2015·2015-05-13

    Eos Imaging Recalls EOS Digital Radiography Systems Due to Filtration Alert Issue

    Eos Imaging Inc is recalling 13 EOS digital radiography systems because a software alert regarding X-ray beam filtration may be suppressed, potentially leading to improper filtration during exams.

    Product
    EOS, Digital radiography system used in general radiographic examinations.
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Food)·F-2161-2015·2015-05-13

    Spiceco Recalls Hytop Seasoned Salt for Undeclared Peanut Protein

    Spiceco is recalling Hytop Seasoned Salt because it may contain undeclared peanut protein. The recall includes specific lot numbers distributed nationwide and abroad.

    Product
    Hytop Seasoned Salt Packed for Federated Group, Inc Arlington Heights, IL 60005 a) 5.25 oz. (149 g) UPC 050700083964 b) 16 oz(454 g) UPC 050700482576
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1562-2015·2015-05-13

    Stryker Recalls Trocar Wound Drains Due to Potential Sterility Breach

    Stryker Instruments is voluntarily recalling specific trocar wound drains and ambulating bulbs because of a potential sterility breach in the packaging.

    Product
    3/16 in. Trocar with Single Drain Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved trocar wound drain has a curved metal trocar attached to one end of the flexible wound drain tube. There is also a polymeric trocar guard that provides protection from…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2181-2015·2015-05-13

    Cott Beverages Recalls Kroger Tropical Mango Shots for Unlabeled Walnut

    Cott Beverages is recalling Kroger Shots Tropical Mango Flavor 2 packs because they may contain trace amounts of walnut, a tree nut not listed on the ingredient label.

    Product
    Kroger Shots Tropical Mango Flavor 2 pack
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-2154-2015·2015-05-13

    Spiceco Recalls Emeril's Cajun Seasoning Blend Due to Undeclared Peanut

    Spiceco is recalling Emeril's Cajun Seasoning Blend because it may contain undeclared peanut protein. The recall includes 2,458 cases distributed nationwide and abroad.

    Product
    Emeril's Cajun Seasoning Blend, 3.45 oz. (98g) Distributed by: B&G Foods, Inc., Parsippany, NJ 07054 USA, UPC 07468309979
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1595-2015·2015-05-13

    ICU Medical Recalls 98-inch Transfer Sets Due to Connection Separation

    ICU Medical is recalling 50 units of 98-inch Transfer Sets because potential connection separation could lead to leakage.

    Product
    98" (249 cm) Transfer Set w/MicroClave T-Connector, 2 Check Valves, Luer Lock, Non-DEHP Tubing, Item No. B3372 Product Usage: IV Administration sets are intended for the infusion and withdrawal of fluids. The devices are provided sterile.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1564-2015·2015-05-13

    Stryker Recalls Wound Drains for Potential Sterility Breach

    Stryker Instruments is voluntarily recalling CBCII Wound Drains and Ambulating Bulbs due to a potential sterility breach in the packaging.

    Product
    1/8 in. Trocar with Single Drain Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved trocar wound drain has a curved metal trocar attached to one end of the flexible wound drain tube. There is also a polymeric trocar guard that provides protection from…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1567-2015·2015-05-13

    Stryker Recalls Wound Drains and Ambulating Bulb for Sterility Breach

    Stryker Instruments is voluntarily recalling specific wound drain and ambulating bulb products due to a potential sterility breach in the packaging.

    Product
    1/4 in. Double Trocar with Wound Drain Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved trocar wound drain has a curved metal trocar attached to one end of the flexible wound drain tube. There is also a polymeric trocar guard that provides protection…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1589-2015·2015-05-13

    ICU Medical Recalls MicroClave T-Connectors Due to Potential Leakage

    ICU Medical is recalling MicroClave T-Connectors because potential connection separation issues could lead to leakage.

    Product
    107" (272 cm) Ext Set w/2 Check Valves, MicroClave T-Connector, Clamp, Rotating Luer, Non-DEHP Tubing, Item No. B33041 Product Usage: IV Administration sets are intended for the infusion and withdrawal of fluids. The devices are provided sterile.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2158-2015·2015-05-13

    Spiceco Recalls Chicken Seasoning and Paprika Due to Undeclared Peanut

    Spiceco is recalling Shoppers Value Chicken Seasoning and Pride of Szeged Sweet Hungarian Paprika because they may contain undeclared peanut protein.

    Product
    Shoppers Value Chicken Seasoning 5 oz. - UPC 041130310676 Distributed By: Supervalu Inc., Eden Prairie, MN 55344 USA,
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2167-2015·2015-05-13

    Spiceco Recalls Seasoning Salt and Paprika for Undeclared Peanut

    Spiceco is recalling Twin Tree Gardens Seasoning Salt and Pride of Szeged Paprika because they may contain undeclared peanut protein.

    Product
    Twin Tree Gardens Premium Spice Blends Seasoning Salt Net 5.5 oz (155 g) Distributed to Flavor Delite, Inc. Reinburg South Carolina PC4016
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1576-2015·2015-05-13

    B. Braun Medical Recalls Pain Control Trays Due to Sterile Barrier Risk

    B. Braun Medical is recalling specific pain control trays because a potential hole in the outer tray may compromise the sterile barrier, posing a risk of contamination.

    Product
    CONTIPLEX Continuous Peripheral Nerve Block Tray, CONTIPLEX Stirn Continuous Nerve Block Tray, Custom Epidural and Anesthesia Tray, Custom Epidural Anesthesia Tray, Custom Kit, Custom Single Dose Epidural Anesthesia Tray, Custom Spinal Anesthesia Tray, Custom Spinal Epidural…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2160-2015·2015-05-13

    Spiceco Recalls Seasoning Salt and Paprika for Undeclared Peanut

    Spiceco is recalling Eagle Brand Seasoning Salt and Pride of Szeged Sweet Hungarian Paprika because they may contain undeclared peanut protein.

    Product
    Spice Eagle Brand Seasoning Salt BLN101200 Net Wt: 50 Lbs Packed by : Spiceco Avenel, New Jersey 07001
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2163-2015·2015-05-13

    Spiceco Recalls Chicken Rub and Paprika for Undeclared Peanut

    Spiceco is recalling Redner's Chicken Rub and Sweet Hungarian Paprika because they may contain undeclared peanut protein.

    Product
    Redner's Warehouse Markets Spice Rack Chicken Rub 2.75 oz (77 g) Manufactured for Redner's Warehouse Markets #3 Quarry Road, Reading PA 19605 UPC 015984695937
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2165-2015·2015-05-13

    Spiceco Recalls Chicken Seasoning and Paprika for Undeclared Peanut

    Spiceco is recalling specific lots of chicken seasoning and sweet Hungarian paprika because they may contain undeclared peanut protein.

    Product
    Spice Deluxe Chicken Seasoning Net Wt. 3.5 oz (99 g) Manufactured by Spiceco Terminal Way Avenel, NJ 07001 USA www.spice-co.com UPC 078006000048
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2152-2015·2015-05-13

    Krystyna Bakery Polish Style Cheese Cake Recalled for Undeclared Ingredients

    Krystyna Bakery is recalling 18 oz. Polish Style Cheese Cakes because they contain undeclared ingredients, including whole blueberries and specific food dyes.

    Product
    Krystyna Bakery Polish Style Cheese Cake, Weight 18 oz., UPC 789438000096
    Category
    Food
    Distribution
    1 state

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