The Recall Desk

Archive

January 2017 recalls

913 recalls were announced in January 2017.

What the numbers show

Critical
104
Severe
475
High
175
Moderate
129
Low
30

Of the 913 recalls this month scored against our rubric, 11% are Critical, 52% are Severe.

201–300 of 913

  • SevereFDA (Food)·F-1206-2017·2017-01-18

    All American Seasonings Recalls Guy's Sour Cream & Cheddar Chip Seasoning

    All American Seasonings, Inc. is recalling 12 boxes of Guy's Sour Cream & Cheddar Chip Seasoning due to potential Salmonella contamination.

    Product
    Guy's Sour Cream & Cheddar Chip Seasoning. Product Code: T3040A. 50 lb box
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1210-2017·2017-01-18

    All American Seasonings Recalls Chipotle Ranch Seasoning Due to Salmonella Risk

    All American Seasonings is recalling 29 bags of Chipotle Ranch seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canada.

    Product
    Chipotle Ranch ASI. Product Code: T3883. 33 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1189-2017·2017-01-18

    Valley Milk Products Recalls Non Fat Dry Milk for Salmonella Risk

    Valley Milk Products is recalling Non Fat Dry Milk due to potential Salmonella contamination. The product was distributed to brokers and direct accounts in multiple states.

    Product
    Non Fat Dry Milk, Grade A - High Heat in 50 # bags , manufactured by Valley Milk Products. Stasburg, Virginia 22657 , Permit No. 51-4136 Net Weight - 50 LBS
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Drugs)·D-0428-2017·2017-01-18

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Pharmaceuticals is recalling 1,068,600 Daytrana transdermal patches nationwide because the delivery system failed mechanical peel force specifications.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1185-2017·2017-01-18

    FONA International Recalls Vanilla Type Flavor Due to Salmonella Risk

    FONA International is recalling 1,200 pounds of Vanilla Type Flavor due to possible Salmonella contamination. The product was distributed in Illinois, Wisconsin, New Jersey, Texas, and Canada.

    Product
    Vanilla Type Flavor, Nat & Art, NET WEIGHT: 22.68 KGS, FONA International, Inc., 1900 Averill road, Geneva, IL 60134
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-1197-2017·2017-01-18

    All American Seasonings Recalls Ranch Dressing Pouches for Salmonella Risk

    All American Seasonings, Inc. is recalling 28 pouches of Ranch Dressing due to potential Salmonella contamination. The product was distributed nationwide and to Canada.

    Product
    Ranch Dressing / Hires Big H. Product Code: T3642. 500/14g pouch
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1215-2017·2017-01-18

    All American Seasonings Recalls Xtra Sharp Cheese Sauce Due to Salmonella Risk

    All American Seasonings is recalling 92 bags of Xtra Sharp Cheese Sauce due to potential Salmonella contamination. The product was distributed nationwide and to Canada.

    Product
    Xtra Sharp Cheese Sauce. Product Code: T4015. 37.5 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1229-2017·2017-01-18

    Anderson's Pumpkin Pie Ice Cream Pie Recalled for Undeclared Peanuts

    Anderson's Frozen Custard is recalling 102 Pumpkin Pie ice cream pies sold in New York due to undeclared peanuts.

    Product
    Andersons Pumpkin Pie ice cream pie, 8 inch round ice cream pie with whipped frosting --- The pie is packaged in a 9 inch round clear plastic dome container
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1009-2017·2017-01-18

    Elekta Monaco RTP System Recalled for Incorrect Wedge Calculations

    Elekta is recalling 279 Monaco RTP Systems because they may calculate Enhanced Dynamic Wedge or Virtual Wedge values incorrectly.

    Product
    Monaco RTP System Product Usage: Used to make treatment plans for patients with prescriptions for external beam radiation therapy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0878-2017·2017-01-18

    Hampton Farms Peanut Butter Recalled for High Aflatoxin Levels

    Hampton Farms is recalling 450 lb cans of IBF Peanut Butter because the product was found to contain high levels of aflatoxin.

    Product
    IBF Peanut Butter, Net Weight 450 lbs, Hampton Farms, Severen, NC 27877.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1205-2017·2017-01-18

    All American Seasonings Recalls FH Parmesan Due to Salmonella Risk

    All American Seasonings, Inc. is recalling 50 lb bags of FH Parmesan due to potential Salmonella contamination. The product was distributed nationwide and to Canada.

    Product
    FH Parmesan. Product Code: T206486-50. 50 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1208-2017·2017-01-18

    Condor Snacks Sour Cream & Onion Seasoning Recalled for Salmonella Risk

    All American Seasonings is recalling 238 bags of Condor Snacks Sour Cream & Onion seasoning due to potential Salmonella contamination.

    Product
    Condor Snacks Sour Cream & Onion W/O MSG. Product Code: T3235. 50 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1220-2017·2017-01-18

    Lenny & Larry's Recalls Chocolate Chip Cookies Due to Undeclared Milk

    Lenny & Larry's is recalling specific chocolate chip cookies because dark chocolate chips may contain undeclared milk, posing a risk to consumers with milk allergies.

    Product
    4 oz. Complete Cookie, Chocolate Chip, UPC Code: 7 87692-83461 7, 12pks: 231,114 sleeves (contains 12 cookies) 6pks: 54,660 sleeves (contains 6 cookies) 4pks: 795,528 sleeves (contains 4) Total cookies from all pack sizes above: 6,283,440
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1191-2017·2017-01-18

    All American Seasonings Recalls Biscuits and Gravy Seasoning for Salmonella Risk

    All American Seasonings, Inc. is recalling 44 bags of Biscuits & Gravy Seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canadian consignees.

    Product
    Biscuits & Gravy Seasoning CR/ Barrel O' Fun. Product Code: T3669. 50 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0984-2017·2017-01-18

    Medline E-Z Lubricating Jelly Recalled Due to Lack of Sterilization

    Medline is recalling 12,024 tubes of E-Z Lubricating Jelly because they were not sterilized due to a shipping error.

    Product
    Medline E-Z Lubricating Jelly; Bacteriostatic. Water Soluble. Sterile. 2 FL OZ (59 ml). Product Usage: For medical purposes to lubricate body orifices to facilitate entry of diagnostic or therapeutic devices. Single use only. Sterile if unopened, undamaged package.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1120-2017·2017-01-18

    Sabra Garlic Herb Spread Recalled for Potential Listeria Contamination

    Sabra Dipping Company is recalling Garlic Herb Spreads due to potential Listeria monocytogenes contamination. Consumers should check Best Before dates and discard affected products.

    Product
    Sabra Spreads Garlic Herb, 8.5OZ; UPC 040822343138, SKU301586
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1251-2017·2017-01-18

    Po Folks Cornbread Mix Recalled for Possible Salmonella Contamination

    House-Autry Mills is recalling Po Folks Cornbread Mix because it contains milk product from a supplier recalling for possible Salmonella presence.

    Product
    Po Folks Cornbread Mix, Net Wt., 5 lb bags, UPC Code 0 73484 22509 2
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·F-1232-2017·2017-01-18

    United Food Ingredients Recalls Blue Cheese Snack Seasoning Due to Salmonella Risk

    United Food Ingredients, Inc. is recalling 1,000 lbs of Blue Cheese Snack Seasoning due to potential Salmonella contamination. The product was distributed in Illinois and Wisconsin.

    Product
    United Food Ingredients, Inc. Blue Cheese Snack Seasoning, NET WT. 50.0 lbs., 15W700 South Frontage Road, Burr Ridge, IL 60527
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-1193-2017·2017-01-18

    All American Seasonings Recalls White Cheddar Jalapeno Snack Seasoning

    All American Seasonings is recalling White Cheddar Jalapeno Snack Seasoning due to potential Salmonella contamination. The recall covers 109 bags distributed nationwide and to Canada.

    Product
    White Cheddar Jalapeno Snack Seasoning / Barrel O' Fun. Product Code: T3840. 50 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1115-2017·2017-01-18

    Sabra Supremely Spicy Hummus Recalled for Listeria Risk

    Sabra Dipping Company is recalling Supremely Spicy Hummus due to potential Listeria monocytogenes contamination.

    Product
    Sabra Hummus w/Supremely Spicy, 7 OZ, 10 OZ, 17 OZ UPC SKU ITEM 040822011433 300158 Sabra Hummus Supremely Spicy 7OZ 040822011440 300159 Sabra Hummus Supremely Spicy 10OZ 040822017558…
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1196-2017·2017-01-18

    All American Seasonings Recalls Ranch Seasoning Due to Salmonella Risk

    All American Seasonings is recalling 28 bags of 10 lb Ranch Seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canada.

    Product
    Ranch Seasoning / Letnes/Grizzly's Grill. Product Code: T3576. 10 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1122-2017·2017-01-18

    Sabra Spicy Chili Spread Recalled for Potential Listeria Contamination

    Sabra Dipping Company is recalling Spicy Chili Spreads due to potential Listeria monocytogenes contamination. Consumers should check best-before dates and discard affected products.

    Product
    Sabra Spreads Spicy Chili, 8.5OZ; UPC 040822343145, SKU 301585
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1008-2017·2017-01-18

    Smith & Nephew Recalls Reflection Dead Blow Mallets Due to Weld Cracks

    Smith & Nephew is recalling Reflection Dead Blow Mallets because cracks in the weld allowed lead beads to escape into surgical wounds.

    Product
    REFLECTION(R) DEAD BLOW MALLET, REF 71362106, QTY: (1), NON-STERILE, Smith & Nephew, Inc,. Memphis, TN 38116
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1212-2017·2017-01-18

    All American Seasonings Recalls Jalapeno Popper Seasoning Due to Salmonella Risk

    All American Seasonings is recalling specific lots of Jalapeno Popper seasoning due to potential Salmonella contamination. Consumers should check their lot numbers and stop using the product.

    Product
    Jalapeno Popper ASI. Product Code: T3934. 33 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1201-2017·2017-01-18

    All American Seasonings Recalls Broccoli Cheese Soup Due to Salmonella Risk

    All American Seasonings is recalling 13 bags of 50 lb Broccoli Cheese Soup due to potential Salmonella contamination. The product was distributed nationwide and to Canada.

    Product
    Broccoli Cheese Soup / Comfort Foods. Product Code: T3872. 50 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1124-2017·2017-01-18

    Sabra Hummus Recalled for Potential Listeria Contamination

    Sabra Dipping Company is recalling specific lots of Tuscan Herb Garden hummus due to potential Listeria monocytogenes contamination.

    Product
    Sabra Hummus Tuscan Herb Garden, 17OZ, 32 OZ UPC SKU ITEM 040822330381 301485 Sabra Hummus Tuscan Herb Garden 17OZ 040822330466 300736 Sabra Hummus Tuscan Herb Garden 32OZ
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1216-2017·2017-01-18

    All American Seasonings Recalls Super Nacho Seasoning Due to Salmonella Risk

    All American Seasonings is recalling 50 lb bags of Super Nacho seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canadian consignees.

    Product
    Super Nacho (No-Pho, Gluten Free). Product Code: T4034. 50 lb bags.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1211-2017·2017-01-18

    All American Seasonings Recalls French Onion Seasoning Due to Salmonella Risk

    All American Seasonings, Inc. is recalling 478 bags of French Onion Seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canadian consignees.

    Product
    French Onion Seasoning ASI. Product Code: T3933. 33 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1186-2017·2017-01-18

    FONA International Recalls Nat Cream Flavor Powder for Salmonella Risk

    FONA International is recalling Nat Cream Flavor Powder due to possible Salmonella contamination. The product was distributed in Illinois, Wisconsin, New Jersey, Texas, and Canada.

    Product
    Nat Cream Flavor Powder (WONF), NET WEIGHT 50 LBS, FONA International, Inc., 1900 Averill road, Geneva, IL 60134
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-1020-2017·2017-01-18

    Stryker Recalls Reunion TSA Peg Alignment Sound Due to Breakage

    Stryker Howmedica Osteonics Corp. is recalling 131 units of the Reunion TSA Peg Alignment Sound because the instrument broke during surgery.

    Product
    Reunion TSA Peg Alignment Sound Catalog #5901-1038 The Peg Alignment Sound (PIN 5901-1038, Revision A) is an instrument used in the ReUnion TSA shoulder system for confirming seating height and peg alignment of the TSA Self-Pressurizing Polyethylene Glenoid implant prior to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1243-2017·2017-01-18

    World Food LLC Recalls Chicken Salad on Croissant for Undercooking Risk

    World Food LLC is recalling 30 sandwiches of Chicken Salad on Croissant sold in Florida due to a potential undercooking hazard.

    Product
    Grab & Go Chicken Salad on Croissant Packed by World Food LLC Orlando FL 32837 Net WT 8oz
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1214-2017·2017-01-18

    All American Seasonings Recalls Triple Cheese Blend Due to Salmonella Risk

    All American Seasonings, Inc. is recalling 59 bags of Triple Cheese Blend due to potential Salmonella contamination. The product was distributed nationwide and to Canada.

    Product
    Triple Cheese Blend - No Color. Product Code: T4008. 50 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1198-2017·2017-01-18

    All American Seasonings Recalls Buttermilk Ranch Seasoning for Salmonella Risk

    All American Seasonings, Inc. is recalling 26 boxes of Buttermilk Ranch Snack Seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canada.

    Product
    Buttermilk Ranch Snack Seasoning / Meat Chips. Product Code: T3760. 50 lb box
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1182-2017·2017-01-18

    FDA Recalls Broccoli Cheese Soup with Rice Due to Salmonella Risk

    Copperleaf Kitchen is recalling Country Gardens Cuisine Broccoli Cheese Soup with Rice after a supplier reported positive environmental tests for Salmonella.

    Product
    Country Gardens Cuisine, Singles, Broccoli Cheese Soup with Rice, Net Wt. 1.25 oz (35 grams)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1194-2017·2017-01-18

    All American Seasonings Recalls Non-GMO Sour Cream and Onion Seasoning

    All American Seasonings is recalling 428 bags of Non-GMO Sour Cream & Onion seasoning due to potential Salmonella contamination.

    Product
    Non-GMO Sour Cream & Onion / Deep River Snacks. Product Code: T3527. 50 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1222-2017·2017-01-18

    Linden's Chocolate Chip Cookies Recalled for Undeclared Milk

    Linden Cookies, Inc. is recalling specific packages of Linden's brand Chocolate Chip Cookies because they contain undeclared milk.

    Product
    Linden's brand Chocolate Chip Cookies: a) Chocolate Chippers Bite Size Cookies (Mini), NET WT. 2 OZ., UPC 76809-30017; b) Chocolate Chippers (Mini), NET WT 1.1 OZ., UPC 76809-30090; c) 3 LARGE CHOCOLATE CHIP COOKIES (Pack), NET WT. 1.75 OZ. UPC 76809-30010 --- LINDEN COOKIES…
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·F-1200-2017·2017-01-18

    All American Seasonings Recalls Kay's Naturals Cheese Puff Seasoning

    All American Seasonings is recalling 80 bags of Kay's Naturals Cheese Puff Seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canada.

    Product
    Cheese Puff Seasoning / Kay's Naturals. Product Code: T3852. 50 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1209-2017·2017-01-18

    All American Seasonings Recalls Spicy Nacho Seasoning Due to Salmonella Risk

    All American Seasonings, Inc. is recalling 211 bags of 50 lb Spicy Nacho seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canadian consignees.

    Product
    Spicy Nacho. Product Code: T3552. 50 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1227-2017·2017-01-18

    St. Clair Pistachio Cream Recalled for Salmonella Risk

    St. Clair Foods is recalling Pistachio Cream products due to potential salmonella contamination from an ingredient.

    Product
    Pistachio Cream, packaged under the following brands: (a) St. Clair, product code 104004, ST. CLAIR FOODS, INC., NET WT. 5 LBS (2.27 kg), MEMPHIS, TN 38116, UPC 7717114004 (b) Ron's Home Style Foods, product code 900603, NET WT. 5 LBS(2.27 kg), DIST. BY RON'S HOME STYLE FOODS…
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-0978-2017·2017-01-18

    Alcon Monarch III Cartridge Recalled Due to Potential Lens Lodging

    Alcon Research, Ltd. is recalling 1,130 Monarch III (1) "C" Cartridges because the intraocular lens could become lodged within the device.

    Product
    Alcon Monarch III (1) "C" Cartridge The device is used for implanting AcrySof intraocular lenses in the eye following cataract removal
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0857-2017·2017-01-18

    Koi Palace Mini Moon Cakes Recalled for Undeclared Allergens

    Magic Gourmet Trading Inc. is recalling Koi Palace Mini Moon Cakes due to missing ingredient labels and undeclared peanut oil, wheat, and egg.

    Product
    Koi Palace Mini Moon Cake: Mini Egg Yolk in White Lotus Seed Paste: Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or 8 pieces).
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1234-2017·2017-01-18

    Fourth Street Barbecue Recalls Macaroni and Cheese Due to Salmonella Risk

    Fourth Street Barbecue is voluntarily recalling specific macaroni and cheese products because the powdered cheese packets may contain milk powder contaminated with Salmonella.

    Product
    Cardboard sleeve: Double Takes Macaroni & Cheese Dinner, Distributed By: Greenbrier International, Inc., 500 Volvo Parkway, Chesapeake, VA 23320; Double Takes: Best By: 10/11/17 10/12/17 10/13/17 10/19/17 10/20/17 10/24/17 11/28/17 11/29/17 11/30/17; UPC: 63927701208:
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-0964-2017·2017-01-18

    Stryker Recalls Reprocessed Electrophysiology Catheter Cables Due to Sterility Breach

    Stryker Sustainability Solutions is recalling reprocessed electrophysiology catheter cables because a breach in sterile packaging may have occurred, potentially rendering the product non-sterile.

    Product
    Reprocessed Electrophysiology Catheter Cables Catalog Number: CB3434CT, D134401, CB3410CT, CB3412CT Electrophysiology catheter cables are designed as electrode cables with a multi-pin connector on the distal end and the appropriate number of tails on the proximal end. The…
    Category
    Medical Device
    Distribution
    35 states
  • HighFDA (Food)·F-1093-2017·2017-01-18

    Piazza Produce Recalls Fajita Seasoning for Undeclared Soybean Oil

    Piazza Produce, Inc. is recalling specific lots of Fajita seasoning because the product labeling does not list ingredients, including undeclared soybean oil.

    Product
    Fajita seasoning, 9 lb plastic gallon, product number 63545; Fajita seasoning, 2.5 lb plastic jar, product number 63543
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-1107-2017·2017-01-18

    Piazza Produce Recalls Seasoning Salt for Undeclared Soybean Oil

    Piazza Produce, Inc. is recalling various sizes of seasoning salt because the product labeling does not list ingredients and contains undeclared soybean oil.

    Product
    Seasoning salt, 30 lb plastic pail, product number 68429; Seasoning salt, 8.75 lb plastic gallon, product number 68391; Seasoning salt, 2.5 lb plastic jar, product number 68372; Seasoning salt, 15 lb plastic pail, product number 68410
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-0987-2017·2017-01-18

    Elekta Oncentra Radiation Therapy Software Recalled for Cross Profile Defect

    Elekta, Inc. is recalling Oncentra External Beam and Brachy software because a cross profile for a Varian 60-degree wedge shows 'horns.' The recall covers 433 units distributed worldwide.

    Product
    Oncentra External Beam Oncentra Brachy Product Usage: Oncentra is radiation therapy planning software designed to analyze and plan radiation treatment is three dimensions for the purpose of treating patients with cancer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1095-2017·2017-01-18

    Piazza Produce Garlic Pepper Recalled for Undeclared Soybean Oil

    Piazza Produce, Inc. is recalling Garlic Pepper products because the labels do not list ingredients, including undeclared soybean oil.

    Product
    Garlic Pepper, 6 lb plastic gallon, product number 63964; Garlic Pepper, 1.5 lb plastic jar, product number 63945; Garlic Pepper, 20 lb plastic pail, Product code 64002
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-1218-2017·2017-01-18

    Stonewall Kitchen Orange Cranberry Pancake Mix Recalled for Salmonella Risk

    Stonewall Kitchen is recalling 40 units of Orange Cranberry Pancake & Waffle Mix due to potential salmonella contamination. The product was distributed in six states.

    Product
    Stonewall Kitchen Orange Cranberry Pancake & Waffle Mix, Packaged in a 16oz. canister UPC: 711381325971 Item #: 554130
    Category
    Food
    Distribution
    6 states
  • HighFDA (Drugs)·D-0430-2017·2017-01-18

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Pharmaceuticals is recalling Daytrana (methylphenidate) transdermal patches because the delivery system failed to meet mechanical peel force specifications.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0864-2017·2017-01-18

    Koi Palace Mini Moon Cakes Recalled for Undeclared Allergens

    Magic Gourmet Trading Inc. is recalling Koi Palace Mini Moon Cakes due to missing ingredient and allergen labels. Undeclared ingredients include wheat, peanut oil, and pumpkin seed.

    Product
    Koi Palace Mini Moon Cake: Single Box - Mini Pumpkin Seed Paste Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or 8 pieces).
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0863-2017·2017-01-18

    Koi Palace Mini Moon Cake Recalled for Undeclared Allergens

    Magic Gourmet Trading Inc. is recalling Koi Palace Mini Moon Cakes because the product lacks adequate labeling, including undeclared wheat flour and peanut oil.

    Product
    Koi Palace Mini Moon Cake: Single Box - Mini Rose Paste Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or 8 pieces).
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0867-2017·2017-01-18

    Koi Palace Mini Mooncakes Recalled for Undeclared Allergens

    Magic Gourmet Trading Inc. is recalling Koi Palace Mini Mooncakes due to missing ingredient labels and undeclared allergens including wheat, peanut oil, and coconut.

    Product
    Koi Palace Mini Moon Cake: Luxury Single Mooncake - Mini Bird's Nest, Black Sesame & Coconut Paste Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or 8 pieces).
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1105-2017·2017-01-18

    Piazza Produce Recalls Quebec Steak Seasoning for Undeclared Soybean Oil

    Piazza Produce, Inc. is recalling Quebec Steak seasoning in three sizes because the product labeling does not list ingredients and contains undeclared soybean oil.

    Product
    Quebec Steak seasoning, 1.5 lb plastic jar, product number 67783; Quebec Steak seasoning, 6 lb plastic gallon, product number 67802; Quebec Steak seasoning, 10 lb plastic pail, product number 67821
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0862-2017·2017-01-18

    Koi Palace Mini Moon Cakes Recalled for Undeclared Allergens

    Magic Gourmet Trading Inc. is recalling Koi Palace Mini Moon Cakes because they lack adequate labeling and contain undeclared allergens.

    Product
    Koi Palace Mini Moon Cake: Dalmaji with Happy Family Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or 8 pieces).
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0858-2017·2017-01-18

    Koi Palace Mini Moon Cakes Recalled for Undeclared Allergens

    Magic Gourmet Trading Inc. is recalling Koi Palace Mini Moon Cakes due to missing ingredient labels and undeclared wheat, walnuts, and pine nuts.

    Product
    Koi Palace Mini Moon Cake: Mini Fresh Five Nuts with Smoked Ham Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or 8 pieces).
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0877-2017·2017-01-18

    Capitol City Specialties Recalls Peanut Butter Jars for Undeclared Soy Lecithin

    Capitol City Specialties Company is recalling 900 jars of Dashing Thru the Dough Gourmet Chocolate Chip Cookie Dough Peanut Butter due to undeclared soy lecithin.

    Product
    the Peanut Principle, Dashing Thru the Dough, Gourmet Chocolate Chip Cookie Dough Peanut Butter, NET WT 16oz, UPC 609207898788
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0962-2017·2017-01-18

    Medtronic MRI-Conditional Cardiac Devices Recalled for Software Feature Error

    Medtronic is recalling 21,111 MRI-conditional cardiac resynchronization therapy devices because the AdaptivCRT feature may appear enabled when it is not active.

    Product
    Amplia MRI" CRT -D SureScan", Amplia MRI" Quad CRT -D SureScan", Claria MRI" CRT -D SureScan", Claria MRI" Quad CRT -D SureScan. implantable medical devices that automatically detect and treat episodes of ventricular fibrillation, ventricular tachycardia, fast ventricular…
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Food)·F-1252-2017·2017-01-18

    Roy Roger's Pancake Mix Recalled for Possible Salmonella Contamination

    House-Autry Mills is recalling Roy Roger's Pancake Mix because it contains milk product from a supplier recalling for possible Salmonella.

    Product
    Roy Roger's Pancake Mix, Net Wt., 2 lb. 8 oz. bags, UPC Code 0 73484 22724 0
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-0870-2017·2017-01-18

    Koi Palace Mini Mooncakes Recalled for Undeclared Wheat and Peanut Oil

    Magic Gourmet Trading Inc. is recalling Koi Palace Mini Mooncakes due to missing ingredient and allergen labels, specifically for undeclared wheat and peanut oil.

    Product
    Koi Palace Mini Moon Cake: Luxury Single Mooncake - Mini Fresh Jasmine Paste. Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or 8 pieces).
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0967-2017·2017-01-18

    C.R. Bard Recalls Medical Devices Containing Latex Catheters

    C.R. Bard is recalling specific medical device trays and stabilization devices because they contained latex catheters instead of silicone catheters.

    Product
    SURESTEP Tray, BARDEX I.C. COMPLETE CARE, Urine Meter, Temperature STATLOCK Stabilization Device
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-1011-2017·2017-01-18

    Symmetry Surgical ULTRA Sterrad Container Recall for Sealant Defect

    Symmetry Surgical is recalling 149 ULTRA Sterrad containers because deteriorated or missing base trim sealant may allow contaminants to enter the container after sterilization.

    Product
    symmetry surgical ULTRA(R) Sterrad container, REF numbers: C131310-SP, C13134-SP, C13135-SP, C13136-SP, C13139-SP, C13854-SP, C13855-SP, C13856-SP, C181310-SP, C18134-SP, C18135-SP, C18136-SP, C18138-SP, C22854-SP, C22855-SP, C22856-SP, C22858-SP, C24134-SP, C24135-SP…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1223-2017·2017-01-18

    Portland Specialty Baking Recalls White Cake Due to Undeclared Walnut

    Portland Specialty Baking LLC is recalling ALN UNICED 1/4 Sheet Split Layer White Cake because it may contain walnut, which is not listed on the label.

    Product
    ALN UNICED 1/4 Sheet Split Layer White Cake, Item 00886, three stacked cake layers with plastic liner in between layers are packaged in a corrugated box, a total of 12 cakes per bulk box. UPC 00750903008862
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1006-2017·2017-01-18

    Philips IQon Spectral CT Recalled for Image and Scan Errors

    Philips is recalling 35 IQon Spectral CT systems due to software issues causing rescans, incorrect scan locations, or misrepresentation of image results.

    Product
    IQon Spectral CT with software version 4.7.0 Product Usage: The IQon Spectral CT is a Computed Tomography X-Ray System intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes. This…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1225-2017·2017-01-18

    Brand Castle Monkey Bread Mix Recalled for Salmonella

    Brand Castle LLC is recalling In The Mix Monkey Bread Mix because the facility and finished product tested positive for Salmonella.

    Product
    In The Mix¿ Monkey Bread Mix NET WT 16 oz (16 lb) 454 g box, INGREDIENTS: BREAD MIX: ***BUTTERMILK*** DISTRIBUTED BY BRAND CASTLE, LLC BEDFORD HTS, OH 44146 www.brandcastle.com UPC 8 44527 03278 2
    Category
    Food
    Distribution
    38 states
  • HighFDA (Food)·F-1217-2017·2017-01-18

    Stonewall Kitchen Cinnamon Apple Pancake Mix Recalled for Salmonella Risk

    Stonewall Kitchen is recalling Cinnamon Apple Pancake & Waffle Mix due to potential Salmonella contamination. Consumers should stop using the product.

    Product
    Stonewall Kitchen Cinnamon Apple Pancake & Waffle Mix, 16 oz. canister UPC: 711381025659 Item #: 551118
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0865-2017·2017-01-18

    Koi Palace Mini Moon Cake Recalled for Undeclared Wheat and Peanut Oil

    Magic Gourmet Trading Inc. is recalling Koi Palace Mini Moon Cakes due to missing ingredient statements and undeclared wheat and peanut oil.

    Product
    Koi Palace Mini Moon Cake: Single Box - Mini Oolong Tea Paste Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or 8 pieces).
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1247-2017·2017-01-18

    House-Autry Buttermilk Biscuit Mix Recalled for Possible Salmonella

    House-Autry Mills is recalling Buttermilk Biscuit Mix because it contains milk from a supplier recalling product due to possible Salmonella.

    Product
    House-Autry Buttermilk Biscuit Mix Tote, Net Wt., 8 oz. (227 g.), UPC Code 0 73484 15500 9,
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-1007-2017·2017-01-18

    Medtronic Recalls AxIEM Touch N Go Pointer Probe for Accuracy Issues

    Medtronic Navigation is voluntarily recalling 111 AxIEM Touch N Go Pointer Probes because they may compromise navigation accuracy during patient registration.

    Product
    AxIEM Touch N Go Pointer Probe. Model Number: 9735318. Placed in a 30mil PETG tray sealed with a Tyvek lid and then placed in a shelf carton.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0861-2017·2017-01-18

    Koi Palace Mini Moon Cakes Recalled for Undeclared Allergens

    Magic Gourmet Trading Inc. is recalling Koi Palace Mini Moon Cakes because they lack adequate labeling and contain undeclared allergens.

    Product
    Koi Palace Mini Moon Cake: Seven Stars Reunion Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or 8 pieces).
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0866-2017·2017-01-18

    Koi Palace Mini Moon Cakes Recalled for Undeclared Allergens

    Magic Gourmet Trading Inc. is recalling Koi Palace Mini Moon Cakes due to missing ingredient and allergen labels for wheat, peanut oil, and walnuts.

    Product
    Koi Palace Mini Moon Cake: Single Box - Mini Walnut, Red Bean Paste Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or 8 pieces).
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1010-2017·2017-01-18

    Symmetry Surgical ULTRA Steam Container Recall for Sealant Defect

    Symmetry Surgical is recalling ULTRA Steam containers because deteriorated or missing base trim sealant may allow contaminants to enter after sterilization.

    Product
    symmetry surgical ULTRA(R) Steam container, REF numbers: C131310, C13134, C13135, C13136, C13139, C13854, C13855, C13856, C181310, C18134, C18135, C18136, C18138, C22854, C22855, C22856, C22858, C24134, C24135, C24136 Product Usage: sterilization container
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1249-2017·2017-01-18

    House-Autry Butterflake Biscuit Mix Recalled for Possible Salmonella

    House-Autry Mills is recalling 606 bags of Butterflake Biscuit Mix because it contains milk product from a supplier recalling for possible Salmonella.

    Product
    House-Autry Butterflake Biscuit Mix, Net Wt. 25 lb. bags, UPC Code 0 73484 20513 1,
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-1250-2017·2017-01-18

    Buddy's Bar-B-Q Hushpuppy Mix Recalled for Possible Salmonella

    House-Autry Mills is recalling Buddy's Bar-B-Q Hushpuppy Mix because it contains milk product from a supplier recalling for possible Salmonella.

    Product
    Buddy's Bar-B-Q Hushpuppy Mix, Net Wt., 5 lb bags, UPC Code 0 73484 22156 2,
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-0966-2017·2017-01-18

    Amendia Recalls Ceres-C Cervical Interbody Devices Due to Missing Pin

    Amendia, Inc. is recalling six Ceres-C Standalone Cervical Interbody devices because they are missing a tantalum market pin.

    Product
    Ceres-C Standalone Cervical Interbody The product is a stand-alone anterior cervical interbody fusion device indicated for use in skeletally mature patients with degenerative disc disease (DDD) with accompanying radicular symptoms at the one level from C2-T1.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-0972-2017·2017-01-18

    Siemens Recalls Artis Q Angiographic X-Ray Systems for Generator Defects

    Siemens is recalling Artis Q angiographic x-ray systems due to potential high-voltage generator failures and rare image display loss.

    Product
    Artis Q/Q.zen, Angiographic x-ray system Stand alone system The Artis systems are a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1235-2017·2017-01-18

    Cheese Club Mac and Cheese Recalled for Salmonella Risk

    Fourth Street Barbecue is recalling Cheese Club mac and cheese products because milk powder ingredients may be contaminated with Salmonella.

    Product
    Cardboard sleeve: Cheese Club express mac Macaroni & Cheese Dinner, Four 2.05 OZ Bowls; Net Wt. 8.2 OZ.; Distributed by: Aldi, Inc., Batavia, IL 60510
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-0988-2017·2017-01-18

    ICU Medical Recalls Tego Connectors Due to Potential Leaking Risk

    ICU Medical is recalling Tego Connectors due to a potential risk of leaking. The devices are used as accessories for vascular access in hemodialysis.

    Product
    Tego Connector, Item No. D1000, NM1000 The Tego¿ Needle Free Access Device is intended for use as an accessory to a vascular access device (catheter) used in Hemodialysis or as an accessory to an Intravascular Administration Set for the administration or withdrawal of fluids…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0868-2017·2017-01-18

    Koi Palace Mini Mooncakes Recalled for Undeclared Allergens

    Magic Gourmet Trading Inc. is recalling Koi Palace Mini Mooncakes due to missing ingredient labels and undeclared wheat, peanut oil, and egg yolk.

    Product
    Koi Palace Mini Moon Cake: Luxury Single Mooncake - Mini White Lotus Seed Paste w/ Egg Yolk Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or 8 pieces).
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1224-2017·2017-01-18

    New Hope Mills Recalls Crepe Mix Due to Salmonella Risk

    New Hope Mills is recalling specific lots of Crepe Mix because the bulk milk powder used may be contaminated with Salmonella.

    Product
    NEW HOPE MILLS Crepe MIX, NET WT. 1 LB. 4 OZ, UPC 074703601529 --- 181 York Street, Auburn, New York 13021 ---Product is packaged in a brown paper bag
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0859-2017·2017-01-18

    Koi Palace Mini Moon Cakes Recalled for Undeclared Allergens

    Magic Gourmet Trading Inc. is recalling Koi Palace Mini Moon Cakes because they lack adequate labeling for undeclared allergens including wheat, gluten, eggs, milk, peanuts, pine nuts, almonds, walnuts, and sesame.

    Product
    Koi Palace Mini Moon Cake: 8 Mini Treasures Combo Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or 8 pieces).
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0963-2017·2017-01-18

    Stryker Recalls Reprocessed Ablation Catheter Cables Due to Sterility Concerns

    Stryker is recalling reprocessed ablation catheter cables because a breach in sterile packaging may have resulted in non-sterile product.

    Product
    Reprocessed Ablation Catheter Cable Catalog Number: CR3425CT, CR3434CT Ablation catheter cables are designed as electrode cables with a multi-pin connector on the distal end which connects to an ablation catheter and a multi-pin connector on the proximal end which connects…
    Category
    Medical Device
    Distribution
    35 states
  • HighFDA (Food)·F-1188-2017·2017-01-18

    Charles Chocolates Toffee Chocolate Macadamia Recalled for Hazelnut Mislabeling

    Charles Chocolates is recalling Toffee Chocolate Macadamia products due to a consumer complaint that the items contained hazelnuts instead of macadamia nuts.

    Product
    Charles Chocolates Toffee Chocolate Macadamia; NET WT. 6.2 oz .(180 grams) UPC: 8 59033 00440 6 Charles Chocolates, San Francisco, CA
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1248-2017·2017-01-18

    House-Autry Cheese Biscuit Mix Recalled for Possible Salmonella

    House-Autry Mills is recalling Cheese Biscuit Mix because it contains milk from a supplier recalling product for possible Salmonella.

    Product
    House-Autry Cheese Biscuit Mix, Net Wt., 8 oz. (227 g.), UPC Code 0 73484 15510 8,
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-1005-2017·2017-01-18

    Philips Clinix RF Plus X-ray System Recalled for Tilt Hazard

    Philips is recalling 41 Clinix RF Plus X-ray systems because liquid penetration can cause an unintentional tilt of the diagnostic table.

    Product
    FV-RF (Clinix RF Plus) Product Usage: A Stationary X-ray System, a device intended for radiographic/fluoroscopic examinations of various anatomical regions. This device may include signal analysis and display equipment, patient and equipment supports, components and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·17V040000·2017-01-18

    Nissan Recalls 2015-2017 Altima Vehicles for Rear Door Latch Defect

    Nissan is recalling 2015-2017 Altima vehicles because improperly routed rear door latch cables may allow doors to open while driving, increasing injury risk.

    Product
    NISSAN — NISSAN ALTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1012-2017·2017-01-18

    Symmetry Surgical ULTRA Gravity Sterilizer Containers Recalled for Sealant Defect

    Symmetry Surgical is recalling 38 ULTRA Gravity sterilizer containers because deteriorated or missing base trim sealant could allow contaminants to enter the container.

    Product
    symmetry surgical ULTRA(R) Gravity container, REF numbers: C131310-G, C13134-G, C13135-G, C13136-G, C13139-G, C13854-G, C13855-G, C13856-G, C181310-G, C18134-G, C18135-G, C18136-G, C18138-G, C22854-G, C22855-G, C22856-G, C22858-G, C24134-G, C24135-G, C24136-G, C24138…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0953-2017·2017-01-18

    In2Bones Recalls NEOVIEW Locking Screws Due to Thread Dimensional Non-Conformity

    In2Bones is recalling 40 units of NEOVIEW locking screws due to dimensional non-conformity of the thread on the screw head. The recall covers units distributed in the US, France, and Switzerland.

    Product
    NEO SCREW 02.7-14MM LOCKING, REF W27 ST114, In2Bones, 28 chemin du petit bois, 69130 Ecully - France The NEOVIEW¿ Plating System is intended for fixation of intra-articular and extraarticular fractures of the distal radius and reconstruction of the distal radius
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1013-2017·2017-01-18

    Beckman Coulter Recalls UniCel DxH 800 Cellular Analysis System

    Beckman Coulter is recalling the UniCel DxH 800 Cellular Analysis System because it may fail to detect blasts in some blood samples.

    Product
    UniCel DxH 800 Coulter Cellular Analysis System, Catalog No. 629029, B24465, B24802, B68304
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0990-2017·2017-01-18

    Varian Eclipse Treatment Planning System Software Recall for Contouring Errors

    Varian Medical Systems is recalling 42 Eclipse Treatment Planning System devices due to a software defect that prevents contours from saving consistently.

    Product
    Eclipse Treatment Planning System version 13.MR2 [13.06.31 with Smart Segmentation Knowledge Based Contouring version 2.3 [2.3.12] Radiology: The Eclipse Treatment Planning System (Eclipse TPS) is used to plan radiotherapy treatments for patients with malignant or benign…
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-1003-2017·2017-01-18

    Corvida Medical Recalls Halo Closed System Transfer Devices Due to Malfunction

    J&J Solutions, Inc. DBA Corvida Medical is recalling 5,520 Halo Closed System Transfer Devices because the needle does not retract. The devices were distributed in Maryland, Texas, and Wisconsin.

    Product
    Halo Closed System Transfer Device, closed syringe adaptor, REF CSA100, Rx only, Sterile, packaged as individual units, packed and shipped 60 units/box and 4 boxes/shipping carton Corvida Medical, Coralville, IA 52241.
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Food)·F-1094-2017·2017-01-18

    Piazza Produce Garden Season No Salt Recalled for Undeclared Soybean Oil

    Piazza Produce is recalling Garden Season No Salt products because the labels do not list soybean oil as an ingredient.

    Product
    Garden season no salt, 5 lb plastic gallon, product number 63516; Garden season no salt, 1.25 lb plastic jar, product number 63514
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0869-2017·2017-01-18

    Koi Palace Mooncakes Recalled for Undeclared Allergens and Labeling Defects

    Magic Gourmet Trading Inc. is recalling Koi Palace Mini Moon Cakes due to inadequate labeling and undeclared allergens including wheat, walnut, pine nut, sesame, and egg yolk.

    Product
    Koi Palace Mini Moon Cake: Luxury Single Mooncake - Mini Fresh Five Nuts with Smoked Ham Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or 8 pieces).
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1246-2017·2017-01-18

    House Autry Corn Bread Mix Recalled for Possible Salmonella

    House-Autry Mills is recalling House Autry Stone Ground Buttermilk Corn Bread Mix because it contains milk product from a supplier recalling for possible Salmonella.

    Product
    House Autry, stone Ground Buttermilk Corn Bread Mix, Net wt. 8 oz. boxes, UPC Code 0 73484 15512 2,
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-0989-2017·2017-01-18

    Health Robotics Recalls i.v. Station Systems Due to Bag Mislabeling

    Health Robotics S.R.L. is recalling 121 i.v. Station and i.v. Station ONCO systems because a motor error caused misalignment and mislabeling of IV bags.

    Product
    i.v. Station and i.v. Station ONCO Automated Drug Compounding System, Pharmacy Compounding System Device Listing Number E454448
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1099-2017·2017-01-18

    Piazza Produce Recalls Italian Herb Seasoning for Undeclared Soybean Oil

    Piazza Produce, Inc. is recalling Italian Herb seasoning in various plastic containers because the product labeling does not list ingredients and contains undeclared soybean oil.

    Product
    Italian Herb seasoning, 6 lb plastic pail, product number 64688; Italian Herb seasoning, 1.5 lb plastic gallon, product number 64667; Italian Herb seasoning, 6 oz plastic jar, product number 64648; Italian Herb seasoning, 3 lb plastic pail, product number 64686
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-1101-2017·2017-01-18

    Piazza Produce Lemon Pepper Recalled for Undeclared Soybean Oil

    Piazza Produce, Inc. is recalling specific Lemon Pepper products because the labels do not list ingredients, including undeclared soybean oil.

    Product
    Lemon Pepper, 5 lb plastic gallon, product number 65085; Lemon Pepper, 1.25 lb plastic jar, product number 65066; Lemon Pepper, 12 lb plastic pail, product number 65104
    Category
    Food
    Distribution
    5 states

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