The Recall Desk

Archive

March 2017 recalls

854 recalls were announced in March 2017.

What the numbers show

Critical
90
Severe
243
High
356
Moderate
134
Low
31

Of the 854 recalls this month scored against our rubric, 11% are Critical, 28% are Severe.

501–600 of 854

  • SevereNHTSA·17V158000·2017-03-10

    Polaris Recalls 2017 Slingshot Models for Steering Bolt Tightening Defect

    Polaris is recalling 2017 Slingshot, SL, and SLR vehicles because three steering and suspension bolts may be insufficiently tightened, potentially reducing vehicle handling.

    Product
    POLARIS — POLARIS SLINGSHOT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V159000·2017-03-10

    Kia Recalls 2017 Niro Hybrid for Power Steering Connector Defect

    Kia is recalling 2017 Niro Hybrid vehicles because a damaged steering connector may cause a loss of power steering assist, increasing the risk of a crash.

    Product
    KIA — KIA NIRO HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17108·2017-03-10

    R.W. Beckett Recalls Firomatic Fuel Oil Valves Due to Fire Hazard

    R.W. Beckett is recalling approximately 18,000 Firomatic fusible safety valves because the stem may fail to seal, allowing fuel to leak and posing a fire hazard.

    Product
    Firomatic® fusible safety valves
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V154000·2017-03-09

    Land Rover Recalls 2016 Range Rovers for Passenger Air Bag Defect

    Jaguar Land Rover is recalling 2016 Range Rover and Range Rover Sport vehicles because the passenger air bag inflator may fail to ignite, preventing deployment in a crash.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER, RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·024-2017·2017-03-09

    Picone Meat Specialties Recalls Pork Salami Due to Undeclared Milk Allergen

    Picone Meat Specialties is recalling approximately 5,750 pounds of pork salami products because they contain non-fat dry milk, a known allergen, that is not declared on the label.

    Product
    Picone Meat Specialties LTD — Picone Meat Specialties, LTD. Recalls Pork Products Due To Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    1 state
  • SevereUSDA FSIS·023-2017·2017-03-09

    King's Command Foods Recalls Beef Products Due to Foreign Matter

    King's Command Foods is recalling approximately 26,138 pounds of ground beef products due to possible contamination with extraneous materials, including metal objects.

    Product
    King's Command Foods, LLC — King's Command Foods, LLC. Recalls Beef Products Due To Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V153000·2017-03-09

    Jaguar Recalls 2017 F-PACE Vehicles Due to Short Rear Driveshaft

    Jaguar is recalling 2017 F-PACE vehicles with automatic transmissions because a short rear driveshaft may separate, causing loss of drive power and increasing crash risk.

    Product
    JAGUAR — JAGUAR F-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V155000·2017-03-09

    Airstream Recalls 2017 Base Camp Trailers Due to Tire Contact Risk

    Airstream is recalling 2017 Base Camp recreational trailers because heavy loads may cause tires to contact the wheel well liner, risking tire failure and crashes.

    Product
    AIRSTREAM — AIRSTREAM BASECAMP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V156000·2017-03-09

    Gillig Recalls 2016-2017 Low Floor Buses for Wiper Arm Defect

    Gillig is recalling 2,732 Low Floor transit buses because wiper arms can crack and detach, reducing driver visibility and increasing crash risk.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17107·2017-03-09

    Pier 1 Imports Recalls Bistro Chairs Due to Fall Hazard

    Pier 1 Imports is recalling Neely and Dahlia bistro chairs because loose bolts can cause the legs to collapse, posing a fall hazard.

    Product
    Neely and Dahlia Bistro Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V157000·2017-03-09

    Manac Recalls 2016-2017 Van Trailers Due to Failing Rub Rail Rivets

    Manac is recalling 2016-2017 Van Trailers because aluminum rivets securing external rub rails may fail, allowing the rails to detach and become road hazards.

    Product
    MANAC — MANAC VAN TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1550-2017·2017-03-08

    Larry The Cable Guy Potato Chips Recalled for Salmonella Risk

    Shearers Foods is recalling Larry The Cable Guy Biscuits & Gravy Thin Potato Chips because ingredients may be contaminated with Salmonella.

    Product
    Larry The Cable Guy Biscuits & Gravy Thin Potato Chips 3 oz bag UPC 7 67212 62423 & 8 oz bag UPC 7 67212 62461
    Category
    Food
    Distribution
    11 states
  • CriticalFDA (Drugs)·D-0505-2017·2017-03-08

    Pacific Medical Solutions Recalls Nano PNC Water Due to Bacterial Contamination

    Pacific Medical Solutions is recalling Nano PNC Water because it was marketed without FDA approval and tested positive for the bacterium variovorax paradoxus.

    Product
    Nano PNC Water, packaged in amber glass bottles, Rx only, ICRPstudy.com, Immune Cellular Restoration Program.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1539-2017·2017-03-08

    Foxy's Oregon Cherry Vanilla Ice Cream Recalled for Listeria Risk

    Altijira Murray Products, LLC is recalling Foxy's Oregon Cherry Vanilla 1 Pint ice cream due to potential Listeria monocytogenes contamination. The product was distributed in California and New York.

    Product
    foxy's oregon cherry vanilla 1 Pint
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-1538-2017·2017-03-08

    Altijira Murray Products Recalls Vanilla Ice Cream for Listeria Risk

    Altijira Murray Products, LLC is recalling foxy's rather thoughtful vanilla 1 Pint ice cream due to potential Listeria monocytogenes contamination. The product was distributed in California and New York.

    Product
    foxy's rather thoughtful vanilla 1 Pint
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-1548-2017·2017-03-08

    Deep River Sour Cream & Onion Chips Recalled for Salmonella Risk

    Shearers Foods is recalling Deep River Sour Cream & Onion Krinkle Kettle Chips because ingredients from Valley Milk Product may be contaminated with Salmonella.

    Product
    Deep River Sour Cream & Onion Krinkle Kettle Chips 2 oz bag UPC 8 50668 00049 8 & 5 oz bag UPC 8 50668 00099 3
    Category
    Food
    Distribution
    11 states
  • CriticalFDA (Food)·F-1524-2017·2017-03-08

    Tasty Delicious Sugar Bun Recalled for Undeclared Allergens and Dyes

    Tasty Delicious Bakery Inc. is recalling Sugar Buns due to undeclared eggs, milk, and food dyes. The product was distributed in New York and New Jersey.

    Product
    TASTY DELICIOUS brand Sugar Bun, Net Wt. 227 Grams (8 Ounces), UPC Code 8 59253 0045 7
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-1543-2017·2017-03-08

    Foxy's Salted Caramel and English Toffee Recalled for Listeria Risk

    Altijira Murray Products, LLC is recalling Foxy's Salted Caramel and English Toffee due to potential Listeria monocytogenes contamination. The product was distributed in California and New York.

    Product
    foxy's salted caramel and english toffee 1 Pint
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-1516-2017·2017-03-08

    Chip 'n Dipped Dark Chocolate Recalled for Undeclared Milk Allergen

    Chip 'n Dipped is recalling 63% Cacao Dark Chocolate due to the presence of an undeclared milk allergen. The product was distributed to retail stores in New York, Pennsylvania, and Massachusetts.

    Product
    63% CACAO DARK Chip 'n Dipped Chocolatier 63% CACAO DARK CHOCOLATE, NET WT. 2.9oz 82g, UPC 892470002161
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-1540-2017·2017-03-08

    Foxy's California Pistachio Recalled for Potential Listeria Contamination

    Altijira Murray Products, LLC is recalling Foxy's California Pistachio 1 Pint due to potential Listeria monocytogenes contamination. The product was distributed in California and New York.

    Product
    foxy's california pistachio 1 Pint
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-1557-2017·2017-03-08

    Papa John's Recalls Co-Jack Cheese Half Moons Due to Listeria Risk

    Papa John's Salads & Produce, Inc. is voluntarily recalling Co-Jack Cheese Half Moons because they may be contaminated with Listeria monocytogenes.

    Product
    Co-Jack Cheese Half Moons, 15pkgs/case UPC 78279600897
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-1561-2017·2017-03-08

    Fred Meyer Whole Wheat Bread Recalled for Undeclared Milk

    The Kroger Co. is recalling Fred Meyer 100% Whole Wheat Bread because it may contain undeclared milk.

    Product
    Fred Meyer 100% Whole Wheat Bread 16 oz plastic bag DISTRIBUTED BY THE KROGER CO. CINCINNATI, OHIO 45202 UPC 0 11110 10294 2
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Drugs)·D-0494-2017·2017-03-08

    Jeffreys Drug Store Recalls Compounded Domperidone Capsules 10 mg

    Jeffreys Drug Store is recalling compounded Domperidone capsules 10 mg because the product was marketed without an approved NDA/ANDA, meaning safety and efficacy have not been established.

    Product
    Domperidone capsules 10 mg, compounded, dispensed in 60, 90, and 360 count bottles, Jeffreys Drug Store 1 North Central Ave. Canonsburg, PA
    Category
    Drug
    Distribution
    1 state
  • CriticalFDA (Food)·F-1552-2017·2017-03-08

    Shearers Foods Recalls Nacho Cheese Tortilla Chips Due to Salmonella Risk

    Shearers Foods is recalling specific bags of nacho cheese tortilla chips because they contain ingredients from a supplier that may be contaminated with Salmonella.

    Product
    NACHO CHEESE TORTILLA CHIPS: Essential Everyday 1 oz bag (Multi-pak) UPC 4 13030 05979; Essential Everyday 1 oz bag UPC 4 13030 59821, 10 oz bag UPC 4 13030 37638 & Market Essential 11.5 oz bag UPC 9 84873 00119
    Category
    Food
    Distribution
    11 states
  • CriticalFDA (Food)·F-1549-2017·2017-03-08

    Shearers Foods Recalls Jalapeno White Cheddar Potato Chips Due to Salmonella Risk

    Shearers Foods is recalling Delish Jalapeno White Cheddar Potato Chips because ingredients from Valley Milk Product may be contaminated with Salmonella.

    Product
    Delish Jalapeno' White Cheddar KETTLE COOKED FLAVORED POTATO CHIPS NET WT 8.5 oz (241g) bag CONTAINS: MILK, UPC 4 49022 83607 5
    Category
    Food
    Distribution
    11 states
  • CriticalFDA (Food)·F-1553-2017·2017-03-08

    Shearers Foods Recalls Spicy Nacho Cheese Tortilla Chips Due to Salmonella Risk

    Shearers Foods is recalling Spicy Nacho Cheese Tortilla Chips because ingredients from Valley Milk Product may be contaminated with Salmonella.

    Product
    SPICY NACHO CHEESE TORTILLA CHIPS: Essential Everyday 10 oz bag UPC 0 41303 06389 7 & Market Essential 11.5 oz bag UPC 0 98487 30014 0
    Category
    Food
    Distribution
    11 states
  • CriticalFDA (Drugs)·D-0496-2017·2017-03-08

    United Exchange Recalls Non-Sterile Eye Wash Bottles Nationwide

    United Exchange Corporation is recalling 46,080 bottles of Eye Wash due to direct evidence of non-sterility contamination in two lots.

    Product
    EYE WASH, 4 fl oz. (118 mL) bottle, OTC, Distributed by: Major Pharmaceutical, 31778 Enterprise Drive, Livonia, MI 48150, Made in Korea, NDC 0904-6491-20
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1558-2017·2017-03-08

    Papa John's Recalls Colby Cheese Half Moons for Listeria Risk

    Papa John's Salads & Produce is voluntarily recalling Colby Cheese Half Moons due to possible Listeria monocytogenes contamination.

    Product
    Colby Cheese Half Moons, 15pkgs/case UPC 78279600898
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-1531-2017·2017-03-08

    ADM Polar Bear Flour Recalled Due to Salmonella Contamination

    ADM Milling Co. is recalling 25,000 pounds of ADM Polar Bear Flour because a product sample tested positive for salmonella. The flour was distributed in Illinois and Indiana.

    Product
    ADM Polar Bear Flour, Bleached/Enriched, NET WT 50LB
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-1537-2017·2017-03-08

    JML Ingredients Recalls IQF Cut Green Beans for Listeria Risk

    JML Ingredients is recalling IQF Cut Green Beans in 20 lb cases due to potential Listeria monocytogenes contamination. The product was distributed in Massachusetts and Pennsylvania.

    Product
    IQF Cut Green Beans; Net Weight 20 lb; Dist. by JML Ingredients, East Petersburg PA, 17520; Packed by: The International Co. for Agri Production & Processing. - ICAPP; Exporter's Address Industrial Zone A - 2 (Lot W) - 10th of Ramadan City - Egypt.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0501-2017·2017-03-08

    G&W Laboratories Recalls Indocin Suppositories for Impurity Failures

    G&W Laboratories is recalling Indocin suppositories due to out-of-specification impurity results found during stability testing.

    Product
    Indocin (Indomethacin) suppositories, USP, 50 mg, laminate strips packed in boxes of 30, Rx only, Manufactured by: G&W Laboratories Inc. South Plainfield, NJ 07080, Distributed by Iroko Pharmaceuticals, LLC Philadelphia, PA 19112, NDC 42211-0102-43
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1368-2017·2017-03-08

    Windstone Medical Packaging Recalls Shoulder Arthroscopy Packs Due to Sterility Risk

    Windstone Medical Packaging is recalling 606 Shoulder Arthroscopy Packs because the included Medtronic gloves may contain splits or holes that compromise sterility.

    Product
    Shoulder Arthroscopy Pack, part number AMS2496(A Shoulder Arthroscopy Pack, part number AMS2496(B Shoulder Arthroscopy Pack, part number AMS2496(C Shoulder Arthroscopy Pack, part number AMS2609 Shoulder Arthroscopy Pack, part number AMS3857 Shoulder Arthroscopy Pack, part…
    Category
    Medical Device
    Distribution
    26 states
  • SevereFDA (Food)·F-1556-2017·2017-03-08

    Papa John's Monterey Jack Cheese Half Moons Recalled for Listeria Risk

    Papa John's Salads & Produce is voluntarily recalling Monterey Jack Cheese Half Moons due to possible Listeria monocytogenes contamination.

    Product
    Monterey Jack Cheese Half Moons, 15pkgs/case UPC 78279600896
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-1329-2017·2017-03-08

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.

    Product
    Lap/Pelviscopy Pack, part number PSS3256(B
    Category
    Medical Device
    Distribution
    26 states
  • SevereFDA (Food)·F-1522-2017·2017-03-08

    Chip 'n Dipped 86% Dark Chocolate Recalled for Undeclared Milk Allergen

    Chip 'n Dipped is recalling 86% Dark Chocolate bars due to the presence of undeclared milk. The product was distributed to retail stores in New York, Pennsylvania, and Massachusetts.

    Product
    86% CACAO DARK, Chip 'n Dipped Chocolatier super smooth 86% DARK CHOCOLATE, NET WT. 2.8oz 79g, UPC 892470002345
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1562-2017·2017-03-08

    Sunrise Growers Recalls Organic IQF Dark Sweet Cherries for Listeria Risk

    Sunrise Growers is recalling organic IQF Dark Sweet Cherries due to possible Listeria monocytogenes contamination. The recall covers 1,800 cases distributed in California.

    Product
    Organic IQF Dark Sweet Cherries, 900 cartons per lot
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1251-2017·2017-03-08

    Olympus Recalls URF-P6 Uretero-reno Fiberscopes Due to Tissue Trauma Risk

    Olympus is recalling URF-P6 and URF-P6R uretero-reno fiberscopes due to adverse events involving tissue trauma and stuck insertion tubes reported in similar devices.

    Product
    URF-P6 Uretero-reno fiberscope and URF-P6R Uretero-reno fiberscope
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V152000·2017-03-08

    Hyundai Recalls Sonata Models Due to Front Seat Belt Defect

    Hyundai is recalling 2011-2015 Sonata and Sonata Hybrid vehicles because front seat belt linkages may detach from anchor pretensioners, increasing injury risk in crashes.

    Product
    HYUNDAI — HYUNDAI SONATA HYBRID, SONATA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0499-2017·2017-03-08

    United Exchange Recalls Eye Wash Bottles Due to Sterility Concerns

    United Exchange Corporation is recalling 190,710 bottles of Eye Wash due to a lack of assurance of sterility. The product was distributed nationwide, in Puerto Rico, and in Guyana.

    Product
    EYE WASH, 4 fl oz. (118 mL) bottle, OTC, Distributed by: Major Pharmaceutical, 31778 Enterprise Drive, Livonia, MI 48150, Made in Korea, NDC 0904-6491-20
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1536-2017·2017-03-08

    Fred Meyer Recalls Bakery Fresh Goodness Carrot Cupcakes for Undeclared Allergens

    Fred Meyer is recalling Bakery Fresh Goodness Carrot Cupcakes because they contain undeclared milk and soy.

    Product
    Bakery Fresh Goodness Carrot Cupcakes sold in 6 ct. 12 ct. and 25 ct. hard plastic container. Bakery Fresh Goodness Carrot Cupcakes, 6 count package, UPC 41573-27731; Bakery Fresh Goodness Carrot Cupcakes, 12 count package, UPC 41573-27732; Bakery Fresh Goodness Carrot…
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-1519-2017·2017-03-08

    Chip'n Dipped Dark Almond Chocolate Bars Recalled for Undeclared Milk

    Chip'n Dipped is recalling Dark Almond 63% Cacao chocolate bars because they contain undeclared milk. The product was sold in New York, Pennsylvania, and Massachusetts.

    Product
    DARK ALMOND 63% CACAO, Chip 'n Dipped Chocolatier, DARK SEA SALTED ALMOND, NET WT. 3.0oz 85g, UPC 892470002185
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1518-2017·2017-03-08

    Chip'n Dipped Dark Pretzel Chocolate Bars Recalled for Undeclared Milk

    Chip'n Dipped is recalling Dark Pretzel 63% Cacao chocolate bars because they contain undeclared milk. The product was sold in New York, Pennsylvania, and Massachusetts.

    Product
    DARK PRETZEL 63% CACAO, Chip 'n Dipped Chocolatier, CRISP & SALTY DARK CHOCOLATE PRETZEL, NET WT. 2.9oz 82g, UPC 892470002222
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-0788-2017·2017-03-08

    Medtronic SynchroMed II Software Card Recall for Priming Bolus Function

    Medtronic is recalling 22,298 SynchroMed II software application cards to update the priming bolus function and pump labeling.

    Product
    Medtronic SynchroMed II Implantable Drug Infusion System. This system includes: Model 8870 Software Application Card, Model 8840 N'Vision Clinician Programmer, and Model 8637 SynchroMed II Implantable Drug Infusion Pump (supplied in 20 ml or 40 ml reservoir size.) Product…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1379-2017·2017-03-08

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are being recalled because splits or holes may compromise sterility.

    Product
    Upper Torso Tray, part number PSS1554(B
    Category
    Medical Device
    Distribution
    26 states
  • SevereFDA (Food)·F-1515-2017·2017-03-08

    Chip 'n Dipped Dark Chocolate Crunch Recalled for Undeclared Milk Allergen

    Chip 'n Dipped is recalling Dark Chocolate Crunch bars because they contain undeclared milk. The product was sold in New York, Pennsylvania, and Massachusetts.

    Product
    DARK CRUNCH Chip 'n Dipped Chocolatier DARK CHOCOLATE CRUNCH, NET WT. 2.9oz 82g, UPC 892470002246
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1520-2017·2017-03-08

    Chip'n Dipped Dark Chocolate Recalled for Undeclared Milk Allergen

    Chip'n Dipped is recalling specific lots of HOT Dark Chocolate with Habanero Pepper due to the presence of undeclared milk.

    Product
    HOT 63% CACAO, Chip 'n Dipped Chocolatier, HOT DARK CHOCOLATE with HABANERO PEPPER, NET WT. 2.8oz 79g, UPC 892470002581
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0497-2017·2017-03-08

    United Exchange Recalls Eye Irrigating Solution Due to Sterility Concerns

    United Exchange Corporation is recalling 112,320 bottles of Eye Irrigating Solution because the product lacks assurance of sterility.

    Product
    Eye Irrigating Solution, 4 fl oz (118 mL) bottle, OTC, Distributed by: Rugby Laboratories, 31778 Enterprise Drive, Livonia, MI 48150, Made in Korea, NDC 0536-1083-97
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0498-2017·2017-03-08

    United Exchange Eye Wash Recalled Due to Lack of Sterility Assurance

    United Exchange Corporation is recalling 77,184 bottles of Eye Wash because the product lacks assurance of sterility. The recall covers specific lots distributed nationwide, in Puerto Rico, and in Guyana.

    Product
    Eye Wash, 4 fl oz (118 mL) bottle, OTC, Distributed by: United Exchange Corp., 17211 Valley View Ave., Cerritos, CA 90703, Made in Korea, UPC Code: 780707005828
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1521-2017·2017-03-08

    Chip n Dipped 72% Dark Chocolate Recalled for Undeclared Milk Allergen

    Chip'n Dipped is recalling 72% Cacao Dark Chocolate bars because they contain undeclared milk, an allergen not listed on the label. This poses a risk to consumers with milk allergies.

    Product
    72% CACAO DARK, Chip 'n Dipped Chocolatier extra dark 72% DARK CHOCOLATE, NET WT. 2.8oz 79g, UPC 89247002338
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1555-2017·2017-03-08

    Papa John's Recalls Pepper Jack Cheese Half Moons for Listeria Risk

    Papa John's Salads & Produce is voluntarily recalling Pepper Jack Cheese Half Moons due to possible Listeria monocytogenes contamination.

    Product
    Pepper Jack Cheese Half Moons, 15pkgs/case UPC 78279600895
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-1517-2017·2017-03-08

    Chip'n Dipped Dark Chocolate Marshmallow Sundae Recalled for Undeclared Milk

    Chip'n Dipped is recalling Dark Chocolate Marshmallow Sundae products due to the presence of undeclared milk allergen.

    Product
    MARSHMALLOW SUNDAE, Chip 'n Dipped Chocolatier DARK CHOCOLATE MARSHMALLOW SUNDAE, NET WT. 3.1oz 88g, UPC 892470002611
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0491-2017·2017-03-08

    Mylan Recalls Glipizide Extended-Release Tablets Due to Foreign Tablet Presence

    Mylan Pharmaceuticals is recalling 1,338 bottles of Glipizide 5 mg Extended-Release Tablets because they may contain 10 mg tablets.

    Product
    glipiZIDE Extended-Release Tablets, 5 mg, 1000 count bottles, Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV --- NDC 0378-0342-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1252-2017·2017-03-08

    Olympus Uretero-reno Videoscope Recall Due to Insertion Tube Breakage

    Olympus is recalling URF-V2 and URF-V2R endoscopes because the insertion tube bending section may break during surgery, causing tissue trauma.

    Product
    Uretero-reno videoscope URF-V2 and URF-V2R endoscope and accessories The URF-V2/V2R endoscopes are intended for use in endoscopic diagnosis and treatment within the ureter and kidney.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1363-2017·2017-03-08

    Windstone Medical Packaging Recalls Podiatry Packs Due to Sterility Concerns

    Windstone Medical Packaging is recalling 2,018 Podiatry Packs because the disposable gloves included may have splits or holes that compromise sterility.

    Product
    Podiatry Pack, part number AMS2778 Podiatry Pack, part number AMS2778(A Podiatry Pack, part number AMS3785(B Podiatry Pack, part number AMS3785(C Podiatry Pack, part number AMS4011(A Podiatry Pack, part number PSS3422(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1384-2017·2017-03-08

    Beckman Coulter iChemVELOCITY Urine Chemistry System Recalled for Probe Misalignment

    Beckman Coulter is recalling iChemVELOCITY Urine Chemistry Systems because probe misalignment or bending can lead to delayed or incorrect patient results.

    Product
    iChemVELOCITY Urine Chemistry System, Catalog No. 800-3530, 800-7167, 800-7719, 800-7720, 800-3564, 800-7100, 800-7103, 800-7106, 800-7162, 800-7163, 800-7166, 800-3061. The iChem Velocity automated urine chemistry system is used to test for the following analytes in urine…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1332-2017·2017-03-08

    Windstone Medical Packaging Recalls Laparotomy Packs Due to Sterility Concerns

    Windstone Medical Packaging is recalling 331 laparotomy packs because the disposable gloves inside may contain splits or holes that compromise sterility.

    Product
    Laparotomy Pack, part number 006268-9 Laparotomy Pack, part number AMS4418(A Laparotomy Pack, part number PSS2190(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Food)·F-1545-2017·2017-03-08

    Bell Stone Toffee Recalls White Chocolate Toffee for Undeclared Milk Allergen

    Bell Stone Toffee is voluntarily recalling White Chocolate Toffee because the label declared butter but failed to identify the presence of the milk allergen.

    Product
    White Chocolate Toffee, 2.2oz pouches, 6oz pouches, 7oz boxes, one pound boxes
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-1322-2017·2017-03-08

    Windstone Medical Knee Scope Packs Recalled for Sterility Compromise

    Windstone Medical Packaging is recalling 156 Knee Scope Packs because the disposable gloves included may have splits or holes that compromise sterility.

    Product
    Knee Scope Pack, part number AMS2498(A Knee Scope Pack, part number AMS2498(B Knee Scope Pack, part number AMS2498(C
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1355-2017·2017-03-08

    Windstone Medical Packaging Recalls Ortho Packs with Defective Gloves

    Windstone Medical Packaging is recalling 84 Ortho Pack kits because the included Medtronic gloves may have splits or holes that compromise sterility.

    Product
    Ortho Pack, part number PSS3466(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1294-2017·2017-03-08

    Windstone Medical ENT Packs Recalled for Potential Sterility Compromise

    Windstone Medical Packaging is recalling 390 ENT Packs because the included Medtronic gloves may contain splits or holes that compromise sterility.

    Product
    ENT Pack, part number AMS3237(A ENT Pack, part number AMS4214
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1388-2017·2017-03-08

    Cook Inc. Recalls Check-Flo Performer Introducer Sets Due to Blood Loss Risk

    Cook Inc. is recalling 854 Check-Flo Performer Introducer Sets because a specific valve design is associated with increased reports of blood loss.

    Product
    Check-Flo Performer Introducer Set, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers are intended for introduction of balloons, closed and non-tapered end catheters or other diagnostic and interventional devices.
    Category
    Medical Device
    Distribution
    46 states
  • HighFDA (Devices)·Z-1350-2017·2017-03-08

    Windstone Medical Packaging Recalls Open Procedure Packs Due to Sterility Concerns

    Windstone Medical Packaging is recalling 1,125 Open Procedure Packs because the disposable gloves included may have splits or holes that compromise sterility.

    Product
    Open Procedure Pack, part number AMS4596 Open Procedure Pack, part number AMS4596(A Open Procedure Pack, part number AMS4596(B
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1281-2017·2017-03-08

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are being recalled because splits or holes may compromise sterility.

    Product
    Chest Breast Drape, part number AMS5853
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1380-2017·2017-03-08

    Windstone Medical Recalls Vascular Packs Due to Sterility Compromise

    Windstone Medical Packaging is recalling 360 Vascular Packs because the disposable gloves inside may contain splits or holes that compromise sterility.

    Product
    Vascular Pack, part number AMS4030 Vascular Pack, part number AMS4030(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1334-2017·2017-03-08

    Windstone Medical Liposuction Kits Recalled for Potential Sterility Compromise

    Windstone Medical Packaging recalled 35 liposuction kits because the included Medtronic gloves may contain splits or holes that compromise sterility.

    Product
    Liposuction Pack, part number AMS3323(B Liposuction Pack, part number AMS5684 Liposuction Pack, part number AMS5699
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1352-2017·2017-03-08

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

    Windstone Medical Packaging is recalling Opgrande Hand Packs containing Medtronic gloves due to potential splits or holes that may compromise sterility.

    Product
    Opgrande Hand Pack, part number AMS4767
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1369-2017·2017-03-08

    Windstone Medical Packaging Recalls Shoulder Packs with Defective Gloves

    Windstone Medical Packaging is recalling 875 Shoulder Pack kits because the included Medtronic gloves may contain splits or holes that compromise sterility.

    Product
    Shoulder Pack, part number AMS2936 Shoulder Pack, part number AMS3638 Shoulder Pack, part number AMS3711(B Shoulder Pack, part numbere AMS4212 Shoulder Pack, part number AMS6460 Shoulder Pack, part numberPSS1852(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1255-2017·2017-03-08

    Siemens ADVIA Centaur Calibrator A Kits Recalled for FT4 Bias

    Siemens is recalling specific Calibrator A Kits due to a negative bias in FT4 assays and potential calibration failures on certain systems.

    Product
    Siemens ADVIA Centaur Systems Calibrator A Kits, Cat No. 04800646, SMN 10285903 (2 pack)Cat No. 04800735, SMN 10285904 (6 pack) Cat No. 04800840, SMN 10285905 (6 pack - REF)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1260-2017·2017-03-08

    Windstone Medical Recalls Anterior Cervical Fusion Packs Due to Sterility Risk

    Windstone Medical Packaging is recalling 51 Anterior Cervical Fusion Packs because the disposable gloves included in the kits may contain splits or holes that compromise sterility.

    Product
    Anterior Cervical Fusion Pack, part number AMS2502(A Anterior Cervical Fusion Pack, part number AMS2502(C
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1304-2017·2017-03-08

    Windstone Medical Recalls General Laparoscopy Packs Due to Sterility Concerns

    Windstone Medical Packaging is recalling 36 General Laparoscopy Packs because the disposable gloves included may have splits or holes that compromise sterility.

    Product
    General Laparoscopy Pack, part number AMS4798 General Laparoscopy Pack, part number AMS4798(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Food)·F-1559-2017·2017-03-08

    Gamay Foods Recalls Cheddar Cheese Seasoning Due to Salmonella Concerns

    Gamay Foods Inc is recalling Original Cheddar Cheese Seasoning because a milk powder ingredient was recalled for potential Salmonella contamination.

    Product
    Original Cheddar Cheese Seasoning, #117059, Net Weight 1600 lbs. bulk tote
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1295-2017·2017-03-08

    Windstone Medical Recalls Extremity Packs Due to Potential Sterility Compromise

    Windstone Medical Packaging is recalling 810 Extremity Packs because the disposable gloves inside may contain splits or holes that compromise sterility.

    Product
    Extremity Pack, part number AMS3240 Extremity Pack, part number AMS4764 Extremity Pack, part number AMS4788(A Extremity Pack, part number PSS1798(A Extremity Pack, part number PSS1798(A Extremity Pack, part number PSS1798(A Extremity Pack, part number PSS1842(A Extremity…
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1267-2017·2017-03-08

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.

    Product
    Basic Pack, part number AMS1868(B Basic Pack, part number AMS2608(A Basic Pack, part number AMS3861 Basic Pack, part number AMS4309 Basic Pack, part number PSS1833 Basic Pack, part number PSS1833(A Basic Pack, part number PSS1848(A
    Category
    Medical Device
    Distribution
    26 states

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