The Recall Desk

Archive

December 2016 recalls

806 recalls were announced in December 2016.

What the numbers show

Critical
107
Severe
181
High
298
Moderate
178
Low
42

Of the 806 recalls this month scored against our rubric, 13% are Critical, 22% are Severe.

101–200 of 806

  • HighFDA (Food)·F-0797-2017·2016-12-28

    Crescent Vending Recalls Roast Beef and Cheddar Sandwiches for Undeclared Allergens

    Crescent Vending Co. Inc. is recalling 11 roast beef and cheddar cheese sandwiches on Kaiser rolls due to undeclared wheat, soy, and milk allergens.

    Product
    Roast Beef and Cheddar Cheese on Kaiser Roll wrapped in clear film, 5 oz. Undeclared allergens - Wheat, Soy (oil, flour), Milk
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0898-2017·2016-12-28

    Teleflex Recalls Mucosal Atomization Devices Due to Incomplete Atomization

    Teleflex Medical is recalling Mucosal Atomization Devices because they may produce a straight stream instead of a fully atomized plume of medication.

    Product
    Mucosal Atomization Device (MAD), Intranasal Mucosal Atomization Device with 3mL Syringe and Vial Adapter; Product Code MAD100, MAD100OS MAD110, MAD110OS, MAD130, MAD130OS, MAD140, MAD140OS, MAD300, MAD300B. Manufactured By: Wolfe-Tory Medical, Inc., Teleflex Medical. For atomiz
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0799-2017·2016-12-28

    Oscor Medical Sheath Recall Due to Inner Liner Fragmentation

    Oscor, Inc. is recalling 21 units of the Adelante Breezway 8F Straight sheath because a fragment of the inner liner detached during insertion.

    Product
    OSCOR ADELANTE BREEZWAY 8F STRAIGHT S79CM D84CM Catalog # AB081211 Is designed to facilitate the introduction of catheters to any of the heart chambers, including the left atrium via a transseptal puncture.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0792-2017·2016-12-28

    Oscor Medical Sheath Recalled Due to Inner Liner Fragmentation

    Oscor, Inc. is recalling 30 units of the Adelante Breezeway sheath because a fragment of the inner liner detached during insertion.

    Product
    OSCOR ADELANTE BREEZEWAY 8F C90¿ S61CM D66CM Catalog # AB081042 Is designed to facilitate the introduction of catheters to any of the heart chambers, including the left atrium via a transseptal puncture.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0800-2017·2016-12-28

    Oscor Medical Sheath Recalled Due to Inner Liner Fragmentation

    Oscor, Inc. is recalling 22 units of the Adelante Breezeway sheath because a fragment of the inner liner detached during insertion.

    Product
    OSCOR ADELANTE BREEZEWAY 10F C55¿ S61CM D66CM Catalog # AB101072 Is designed to facilitate the introduction of catheters to any of the heart chambers, including the left atrium via a transseptal puncture.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Food)·F-0560-2017·2016-12-28

    Linnane & Co Recalls Frozen Shrimp Cakes for Undeclared Allergens

    Linnane & Co is recalling frozen shrimp cakes because the packaging failed to declare soy, sulfites, Yellow #5, MSG, and an unpermitted food color.

    Product
    Rissois De Camarao Cong. Frozen Shrimp Cakes, Frozen 50 count. Net Weight: 4,50Kg (2 x 2,25Kg) Country of Origin: PORTUGAL
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0795-2017·2016-12-28

    Oscor Medical Sheath Recall Due to Inner Liner Fragmentation

    Oscor, Inc. is recalling 76 units of the Adelante Breezeway sheath because a fragment of the inner liner detached during insertion.

    Product
    OSCOR ADELANTE BREEZEWAY 8F C70¿ S79CM D84CM Catalog # AB081045 Is designed to facilitate the introduction of catheters to any of the heart chambers, including the left atrium via a transseptal puncture.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0813-2017·2016-12-28

    Medtronic Arrive Braided Transseptal Sheath Recalled for Inner Liner Fragmentation

    Oscor, Inc. is recalling 215 units of Medtronic Arrive Braided Transseptal Sheaths because a fragment of the inner liner detached during insertion.

    Product
    MEDTRONIC ARRIVE BRAIDED TRANSSEPTAL SHEATH 10F C90¿ S61CM D66CM GLOBAL Catalog # 990061-090-000 Is designed to facilitate the introduction of catheters to any of the heart chambers, including the left atrium via a transseptal puncture.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0781-2017·2016-12-28

    Nuvectra Recalls Algovita Spinal Cord Stimulation Leads Due to Stylet Protrusion

    Nuvectra is recalling Algovita Spinal Cord Stimulation System percutaneous leads because the stylet may protrude beyond the distal lead tip.

    Product
    Algovita Spinal Cord Stimulation System, Percutaneous Leads, 8-Electrode Percutaneous Lead Kit; Algovita Spinal Cord Stimulation System Percutaneous Leads, 12-Electrode Percutaneous Lead Kit; Algovita Spinal Cord Stimulation System Percutaneous Trial Leads, 8-electrode Lead
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0796-2017·2016-12-28

    Oscor Medical Sheath Recall Due to Inner Liner Fragmentation

    Oscor, Inc. is recalling 61 units of the Adelante Breezeway sheath because a fragment of the inner liner detached during insertion. The product was distributed in the US and internationally.

    Product
    OSCOR ADELANTE BREEZEWAY 8F C90¿ S79CM D84CM Catalog # AB081046 Is designed to facilitate the introduction of catheters to any of the heart chambers, including the left atrium via a transseptal puncture.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0870-2017·2016-12-28

    Stryker Recalls Sterile Minimally Invasive Surgery Burs Due to Corrosion

    Stryker is voluntarily recalling specific lots of sterile MIS Toolsteel Burs because they may exhibit signs of corrosion.

    Product
    8470-009-030 3.0MM Precision Round, 16CM, single use, Sterile The Stryker MIS (Minimally Invasive Surgery) product offering, is used to remove osseous material during surgical cases. Each cutting accessory consists of: " A shank (B) with a notch (A), that fits in the attachmen
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0793-2017·2016-12-28

    Crescent Vending Cheeseburgers Recalled for Undeclared Allergens

    Crescent Vending Co. Inc. is recalling 5 oz. cheeseburgers for failing to declare wheat, soy, and milk allergens.

    Product
    Cheeseburger wrapped in clear film, 5 oz. Undeclared Allergens - Wheat, Soy (Lecithin, oil, flour), Milk,
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0772-2017·2016-12-28

    Wakefern Recalls Oatmeal Raisin Cookies Due to Metal Contamination

    Wakefern Food Corp. is recalling specific packs of Gourmet Oatmeal Raisin Cookies because they may contain metal pieces.

    Product
    12 pack Gourmet Oatmeal Raisin Cookies Net Wt 15 oz. UPC 289784203993 24 pack Gourmet Oatmeal Raisin Cookies Net Wt. 30 oz. UPC 289774706992 Gourmet Oatmeal/Raisin Cookies Net Wt. 30 oz UPC 289771006996
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0802-2017·2016-12-28

    Oscor Medical Sheath Recall Due to Inner Liner Fragmentation

    Oscor, Inc. is recalling eight Adelante Breezeway sheaths because a fragment of the inner liner detached during insertion, posing a risk of device failure.

    Product
    OSCOR ADELANTE BREEZEWAY 10F C120¿ S61CM D66CM Catalog # AB101075 Is designed to facilitate the introduction of catheters to any of the heart chambers, including the left atrium via a transseptal puncture.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Food)·F-0763-2017·2016-12-28

    Fresh Express Caesar Salad Kits Recalled for Undeclared Walnuts

    Fresh Express is recalling Caesar salad kits because the condiment packets contain undeclared walnuts, a tree nut allergen.

    Product
    Fresh Express Kit Caesar salad, Net Wt. 7.6 oz. (215g), Fresh Express Incorporated, 550 S. Caldwell St. Charlotte, NC 28202, packed in clear flexible plastic bags. Product Code: G163B13A
    Category
    Food
    Distribution
    25 states
  • HighFDA (Devices)·Z-0774-2017·2016-12-28

    AngioDynamics Recalls Percutaneous Introducer Sets Due to Detachment Risk

    AngioDynamics is recalling 751 Stiffened Micro-Introducer Kits because a component may detach during use.

    Product
    ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4 F Stiffened Micro-Introducer Kit, 45CM NT/T ECHO B PG, Item Number H787065970505, Catalog No.REF 06597050, 2) 4 F Stiffened Micro-Introducer Kit, 45CM NT/T ECHO S PG, Item Number H787065970525, Catalog No.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0773-2017·2016-12-28

    AngioDynamics Recalls Stiffened Micro-Introducer Kits Due to Component Defect

    AngioDynamics is recalling 80 boxes of Stiffened Micro-Introducer Kits because a component may detach during use.

    Product
    ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4 F Stiffened Micro-Introducer Kit, 45CM SS/T ECHO B PG, Item Number H787065970465, Catalog No.REF 06597046, 2) 4 F Stiffened Micro-Introducer Kit, 45CM SS/T ECHO S PG, Item Number H787065970485, Catalog No.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0798-2017·2016-12-28

    Oscor Medical Sheath Recall Due to Inner Liner Fragmentation During Insertion

    Oscor, Inc. is recalling 26 units of the Adelante Breezeway 8F Straight sheath because a fragment of the inner liner detached during insertion. The defect poses a risk of foreign body introduction into the patient.

    Product
    OSCOR ADELANTE BREEZEWAY 8F STRAIGHT S61CM D66CM Catalog # AB081210 Is designed to facilitate the introduction of catheters to any of the heart chambers, including the left atrium via a transseptal puncture.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0794-2017·2016-12-28

    Oscor Medical Sheath Recall Due to Inner Liner Fragmentation

    Oscor, Inc. is recalling 991 units of the Adelante Breezeway sheath because a fragment of the inner liner detached during insertion.

    Product
    OSCOR ADELANTE BREEZEWAY 8F C55¿ S79CM D84CM Catalog # AB081044 Is designed to facilitate the introduction of catheters to any of the heart chambers, including the left atrium via a transseptal puncture.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Food)·F-0803-2017·2016-12-28

    Crescent Vending Recalls Bacon Egg and Cheese Sandwiches for Undeclared Allergens

    Crescent Vending Co. Inc. is recalling 13 bacon, egg, and cheese sandwiches on Kaiser rolls because they contain undeclared wheat, soy, and milk.

    Product
    Bacon Egg and Cheese on Kaiser Roll wrapped in clear film, 5 oz. Undeclared allergen - Wheat, Soy (oil, lecithin), Milk, Egg
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0830-2017·2016-12-28

    Northern Fish Products Recalls Smoked Fish for Undeclared Soy

    Northern Fish Products is recalling hot smoked salmon, black cod, steelhead, and trout due to undeclared soy.

    Product
    NORTHERN CLASSICS NATURAL SMOKED STEELHEAD*** Product is packaged in bulk 5lb case. Product is vacuum packaged catch weight.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-0885-2017·2016-12-28

    Siemens IMMULITE 2000 PSA Assay Recalled for Hook Effect Performance Issues

    Siemens Healthcare Diagnostics is recalling IMMULITE 2000 PSA assays because they do not meet the High-dose Hook Effect expectations stated in the Instructions for Use.

    Product
    IMMULITE 2000/IMMULITE 2000 XPi Systems Prostate-Specific Antigen (PSA) Assay, REF/Catalog Number L2KPTS2, SMN 10706281 and REF/Catalog Number L2KPTS6, SMN 10706282 (US); REF/Catalog Number L2KPS2, SMN 10380986 and REF/Catalog Number L2KPS6, SMN 10380996 (OUS); IVD --- Origin: UK
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0795-2017·2016-12-28

    Crescent Vending Turkey Sandwiches Recalled for Undeclared Allergens

    Crescent Vending Co. Inc. is recalling 8 oz. Turkey, Bacon and Swiss on Macaroni Salad sandwiches due to undeclared wheat, soy, and milk allergens.

    Product
    Turkey, Bacon and Swiss on Macaroni Salad wrapped in clear film, 8 oz. Undeclared allergens - Wheat, Soy (oil, flour), Milk, Egg
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0791-2017·2016-12-28

    Crescent Vending Recalls Raisin Bagel Sandwiches for Undeclared Allergens

    Crescent Vending Co. Inc. is recalling 26 raisin bagel sandwiches with cream cheese due to undeclared wheat, soy, and milk allergens.

    Product
    Raisin Bagel with Cream Cheese wrapped in clear film, 5 oz. Undeclared allergens - Wheat, Soy (oil), and Milk
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0803-2017·2016-12-28

    Oscor Medical Sheath Recalled Due to Inner Liner Fragmentation

    Oscor, Inc. is recalling 74 units of the Adelante Breezeway sheath because a fragment of the inner liner detached during insertion. The device is used to introduce catheters to heart chambers.

    Product
    OSCOR ADELANTE BREEZEWAY 10F C55¿ S79CM D84CM Catalog # AB101076 Is designed to facilitate the introduction of catheters to any of the heart chambers, including the left atrium via a transseptal puncture.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0805-2017·2016-12-28

    Oscor Medical Sheath Recalled Due to Inner Liner Fragmentation

    Oscor, Inc. is recalling 110 units of the Adelante Breezeway sheath because a fragment of the inner liner detached during insertion.

    Product
    OSCOR ADELANTE BREEZEWAY 10F C90¿ S79CM D84CM Catalog # AB101078 Is designed to facilitate the introduction of catheters to any of the heart chambers, including the left atrium via a transseptal puncture.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Food)·F-0821-2017·2016-12-28

    Northern Fish Products Recalls Smoked Salmon for Undeclared Soy

    Northern Fish Products is recalling hot smoked salmon, black cod, steelhead, and trout due to undeclared soy. The recall excludes hot jerky salmon and jerky salmon.

    Product
    "***NORTHERN CLASSICS NATURAL SMOKED SALMON. Net WT. is filled in on a separate white label. Product is frozen and vacuum packed. Product also referred to as SALMON HOT SMKD SIDE ATL SK-ON.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0829-2017·2016-12-28

    Northern Fish Products Recalls Smoked Fish Due to Undeclared Soy

    Northern Fish Products is recalling hot smoked salmon, black cod, steelhead, and trout because they contain undeclared soy.

    Product
    Brown Sugar Style Smoked Black Cod Black Cod, **Product of USA Packed By Northern Fish Products***" Packaged in bulk 5lb case.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-0789-2017·2016-12-28

    Smiths Medical Recalls Acuvance 2 Safety Catheters Due to Valve Defects

    Smiths Medical is recalling 26,750 Acuvance 2 Safety Catheters because some devices have missing or incorrectly positioned side port valves.

    Product
    Acuvance¿2 Safety Catheter, Product No. 1720-AI Product Usage: The Acuvance¿ 2 Safety Catheter is a Peripheral Intravenous Catheter (PIVC). PIVCs are designed for single use venipuncture on all patient populations where access to the veins and arteries are required. The cath
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0810-2017·2016-12-28

    Brownwood Farms Recalls Yankee Bourbon BBQ Sauce for Undeclared Soy

    Brownwood Farms is recalling Yankee Bourbon BBQ Sauce because it contains soy ingredients not declared on the label.

    Product
    Brownwood Farms Yankee Bourbon BBQ Sauce. 19oz glass bottles and 1 gallon
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0776-2017·2016-12-28

    AngioDynamics Recalls Percutaneous Introducer Sets Due to Detachment Risk

    AngioDynamics is recalling 145 boxes of Stiffened Micro-Introducer Kits because the sheath/dilator components may have a rotating luer that detaches during use.

    Product
    ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4 F Stiffened Micro-Introducer Kit, 45CM SS/T NON-ECHO S PG, Item Number H787065970655, Catalog No.REF 06597065, 2) 4 F Stiffened Micro-Introducer Kit, STF 4F M.I. KIT 45CM NT/T NON-ECHO S PG, Item Number H7
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0771-2017·2016-12-28

    Wakefern Recalls Macadamia Nut Cookies Due to Metal Contamination Risk

    Wakefern Food Corp. is recalling specific macadamia nut cookies because they may contain metal pieces. The products were distributed in six states.

    Product
    12 pack Gourmet White Choc Chunk Macadamia Cookies Net Wt. 15 oz UPC 289783203994 Gourmet White Chocolate Macadamia Nut Cookies Net Wt. 30 oz. UPC 289770006997
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0824-2017·2016-12-28

    Northern Fish Products Recalls Hot Smoked Fish for Undeclared Soy

    Northern Fish Products is recalling hot smoked salmon, black cod, steelhead, and trout due to undeclared soy.

    Product
    ***NORTHERN CLASSICS FINEST QUALITY KIPPERED SALMON CHUNKLETS. This package can be combined with other products and placed into a combination package. Each package is individually labeled. Bulk cases contain 5 lbs.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0943-2017·2016-12-28

    Interbake Foods Recalls Benton's Peanut Butter Cookies Due to Aflatoxin

    Interbake Foods is recalling Benton's Peanut Butter filled Cookies covered in Rich Fudge because a single lot of peanut butter contained elevated aflatoxin levels.

    Product
    Benton's Peanut Butter filled Cookies covered in Rich Fudge, NET WT 9.5 OZ (269 g), UPC 041 498 1896 55, Distributed by ALDI INC. Great Value, Fudge Covered Peanut Butter, 269 g, Imported for Wal-Mart Canada Corp, Product of USA, UPC 6 28915 24342 0.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0770-2017·2016-12-28

    Wakefern Recalls Salted Caramel Cookies Due to Metal Contamination

    Wakefern Food Corp. is recalling specific 12 and 24-pack salted caramel chocolate chunk cookies because they may contain metal pieces.

    Product
    12 pack Gourmet Salted Caramel Chocolate Chunk Cookies - Net Wt.15 oz. UPC 2897850203992 ;UPC 289785003998
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0781-2017·2016-12-28

    Wakefern Recalls Party Candy Cookies Due to Metal Pieces

    Wakefern Food Corp. is recalling 24-count Take&Bake Party Candy Cookies because they may contain metal pieces.

    Product
    24CT Take&Bake Party Candy Cookies Net Wt. 24oz UPC 208902004199
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0765-2017·2016-12-28

    Preferred Meals Cavatappi Pasta Recalled for Possible Listeria Contamination

    Preferred Meal Systems, Inc. is recalling 95,364 units of Cavatappi Pasta with Mascarpone Tomato Cream Sauce due to possible Listeria monocytogenes contamination.

    Product
    Preferred Meals, Cook and Serve, Cavatappi Pasta with Mascarpone Tomato Cream Sauce; 54 9.25 OZ units (NET WEIGHT 31.22 LBS) KEEP FROZEN INSTITUTIONAL USE ONLY
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0794-2017·2016-12-28

    Crescent Vending Recalls Hot Sausage Sandwiches for Undeclared Allergens

    Crescent Vending Co. Inc. is recalling 6 oz. Hot Sausage on Club sandwiches because they contain undeclared wheat, soy, and milk.

    Product
    Hot Sausage on Club wrapped in clear film, 6 oz. Undeclared allergens - Wheat, Soy (oil)
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0900-2017·2016-12-28

    Exactech Recalls Equinoxe Reverse Shoulder Screw Kits Due to Disengaged Heads

    Exactech, Inc. is recalling 2,278 Equinoxe Reverse Shoulder Fixed Angle Torque Defining Screw Kits because disengaged screw heads may not be retained in the screwdriver.

    Product
    Equinoxe Reverse Shoulder Fixed Angle Torque Defining Screw Kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0826-2017·2016-12-28

    Northern Fish Products Recalls Hot Smoked Salmon Due to Undeclared Soy

    Northern Fish Products is recalling hot smoked salmon, black cod, steelhead, and trout because they contain undeclared soy.

    Product
    PREMIUM SMOKED SALMON UPC 7 02772 00564 0 Packaged in a 5 lb case 20/4oz vacuum packaged per case. Cardboard type label is folded over and affixed to the top of the package. Sell by date is marked on the label by the consignee.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0796-2017·2016-12-28

    Crescent Vending Recalls Imported Ham Sandwiches for Undeclared Allergens

    Crescent Vending Co. Inc. is recalling 13 imported ham sandwiches with potato salad due to undeclared wheat, soy, and milk allergens.

    Product
    Imported Ham with Potato salad wrapped in clear film, 8 oz. Undeclared allergens - Wheat, Soy (oil), Milk, Egg
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0798-2017·2016-12-28

    Crescent Vending Recalls Ham and Cheese Sandwiches for Undeclared Allergens

    Crescent Vending Co. Inc. is recalling 19 ham and cheese sandwiches distributed in Pennsylvania because they contain undeclared wheat, soy, and milk.

    Product
    Ham and Cheese on Club wrapped in clear film, 5 oz. Undeclared allergens - Wheat, Soy (oil, lecithin), Milk
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0808-2017·2016-12-28

    Crescent Vending Hot Dog Sandwiches Recalled for Undeclared Allergens

    Crescent Vending Co. Inc. is recalling 18 hot dog sandwiches for failing to declare wheat, soy, and milk allergens.

    Product
    1/4 1b. Hot Dog with Cheese wrapped in clear film, 6 oz. Undeclared allergens - Wheat, Soy(oil, lecithin) Milk
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0886-2017·2016-12-28

    Amendia Recalls Black Widow Spinal Plates Due to Mating Feature Defect

    Amendia, Inc. is recalling 48 units of Black Widow Buttress Plates due to a design defect in the mating feature between the plate and screw.

    Product
    Black Widow Plate 19mm Plate, Part Number TBP119; Black Widow Plate 23mm Plate, Part Number TBP123 The Black Widow Buttress Plates and Screws are designed for preventing migration or expulsion of allograft or autograft in the thoracolumbar to S1 Spinal region
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0814-2017·2016-12-28

    Medtronic Arrive Braided Transseptal Sheath Recalled for Inner Liner Fragmentation

    Oscor, Inc. is recalling 186 units of Medtronic Arrive Braided Transseptal Sheaths because a fragment of the inner liner was found during insertion.

    Product
    MEDTRONIC ARRIVE BRAIDED TRANSSEPTAL SHEATH 10F C120¿ S61CM D66CM GLOBAL Catalog # 990061-120-000 Is designed to facilitate the introduction of catheters to any of the heart chambers, including the left atrium via a transseptal puncture.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0784-2017·2016-12-28

    Ultroid Procedure Pack Recalled for Quality System Non-Compliance

    Ultroid Technologies is recalling 52,084 procedure packs because they were not manufactured under required quality system controls.

    Product
    Ultroid Procedure Pack including the Ultroid Sterile Disposable Probes.
    Category
    Medical Device
    Distribution
    34 states
  • HighFDA (Food)·F-0801-2017·2016-12-28

    Crescent Vending Recalls Hoagies for Undeclared Allergens

    Crescent Vending Co. Inc. is recalling 25 Regular Hoagies on Italian Rolls because they contain undeclared wheat, soy, and milk.

    Product
    Regular Hoagie on Italian Roll, wrapped in clear film, 7 oz. Undeclared allergens - Wheat, Soy (oil), Milk
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0892-2017·2016-12-28

    Medtronic Recalls PowerCross .018 OTW PTA Dilatation Catheters

    Medtronic is recalling 315 units of the PowerCross .018 OTW PTA Dilatation Catheter due to a manufacturing defect causing the balloon to fail to inflate or deflate properly.

    Product
    ev3, PowerCross .018 OTW PTA Dilatation Catheter, Sterile EO. The PowerCross .018 OTW PTA Dilatation Catheter is intended to dilate stenoses in the iliac, femoral, ilio-femoral, popliteal, infrapopliteal, and renal arteries, and for the treatment of obstructive lesions of native
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Food)·F-0792-2017·2016-12-28

    Crescent Vending Recalls Egg Salad Sandwiches for Undeclared Allergens

    Crescent Vending Co. Inc. is recalling 13 egg salad sandwiches for failing to declare wheat, soy, and milk allergens.

    Product
    Egg Salad on Wheat wrapped in clear film, 5 oz. Undeclared allergens - Wheat, Soy (oil) and eggs
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0793-2017·2016-12-28

    Oscor Medical Sheath Recalled Due to Inner Liner Fragmentation During Insertion

    Oscor, Inc. is recalling 21 units of the Adelante Breezeway 8F sheath because a fragment of the inner liner detached during insertion. The product is distributed worldwide.

    Product
    OSCOR ADELANTE BREEZEWAY 8F C120¿ S61CM D66CM Catalog # AB081043 Is designed to facilitate the introduction of catheters to any of the heart chambers, including the left atrium via a transseptal puncture.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Food)·F-0764-2017·2016-12-28

    Preferred Meals Tortellini Recalled for Possible Listeria Contamination

    Preferred Meal Systems is recalling Creamy Red Pepper Sauce and Cheese Tortellini due to possible Listeria monocytogenes contamination.

    Product
    Preferred Meals, Cook and Serve, Creamy Red Pepper Sauce and Cheese Tortellini with Parmesan Cheese, 54 9.25 OZ units (NET WEIGHT 31.22 LBS) KEEP FROZEN INSTITUTIONAL USE ONLY
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0831-2017·2016-12-28

    Northern Fish Products Recalls Smoked Fish Due to Undeclared Soy

    Northern Fish Products is recalling hot smoked salmon, black cod, steelhead, and trout because they contain undeclared soy.

    Product
    Smoked Trout Rainbow Trout, NORTHERN FISH PRODUCTS, INC.***" Packaged in bulk 10lb case.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-0775-2017·2016-12-28

    AngioDynamics Recalls Stiffened Micro-Introducer Kits Due to Detachment Risk

    AngioDynamics is recalling 996 boxes of Stiffened Micro-Introducer Kits because the rotating luer on the included sheath/dilator components may detach during use.

    Product
    ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5 F Stiffened Micro-Introducer Kit, 45CM NT/T ECHO B PG, Item Number H787065970515, Catalog No.REF 06597051, 2) 5 F Stiffened Micro-Introducer Kit, 45CM NT/T ECHO S PG, Item Number H787065970535, Catalog N
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0787-2017·2016-12-28

    Wakefern Recalls Double Chocolate Cookies Due to Metal Contamination

    Wakefern Food Corp. is recalling 24-count Double Chocolate Cookies because they may contain metal pieces. The product was distributed in six states.

    Product
    24CT Double Chocolate Cookies Net Wt. 24oz UPC 208722004195
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0827-2017·2016-12-28

    Northern Fish Products Recalls Hot Smoked Salmon Due to Undeclared Soy

    Northern Fish Products is recalling hot smoked salmon, black cod, steelhead, and trout because they contain undeclared soy.

    Product
    Sweet & Spicy Style Atlantic Salmon, Product of USA Packed By Northern Fish Products***" Packaged in bulk 5lb case.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0811-2017·2016-12-28

    Brownwood Farms Cherry BBQ Sauce Recalled for Undeclared Soy

    Brownwood Farms is recalling Cherry BBQ Sauce because it contains soy ingredients that are not declared on the label.

    Product
    Brownwood Farms Cherry BBQ Sauce. 21oz glass bottles, 1 gallon, 5 gallon. Private labels: Arbor Day Farm (Cherry BBQ Sauce). Bowers Harbor Vineyard (Cherry BBQ Sauce 12oz). Benjamin Twiggs (Northwoods Cherry BBQ Sauce 16oz). Crossroads. Friske Orchards. Kimmel Orchard &
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0619-2017·2016-12-28

    Whole Foods 365 Multi Grain Croissant Recalled for Undeclared Eggs

    Whole Foods Market Brand 365 is recalling Multi Grain Croissant 6 PK products due to undeclared eggs. The recall affects select stores in seven states and Washington D.C.

    Product
    MULTI GRAIN CROISSANT 6 PK
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-0618-2017·2016-12-28

    Whole Foods 365 Croissants Recalled for Undeclared Eggs

    Whole Foods Market Brand 365 croissants are being recalled because they contain undeclared eggs, posing a risk to individuals with egg allergies.

    Product
    CROISSANT 6 PK
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-0825-2017·2016-12-28

    Northern Fish Products Recalls Hot Smoked Salmon Due to Undeclared Soy

    Northern Fish Products is recalling hot smoked salmon, black cod, steelhead, and trout because the products contain undeclared soy.

    Product
    PREMIUM SMOKED SALMON***CAJUN***NET WT: 4OZ***Cardboard type label is folded over and affixed to the top of the package. Sell by date is marked on the label by the consignee. UPC 7 02772 00562 6.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0769-2017·2016-12-28

    Wakefern Recalls Gourmet Variety Pack Cookies Due to Metal Pieces

    Wakefern Food Corp. is recalling specific varieties of Gourmet Variety Pack Cookies because they may contain metal pieces.

    Product
    12 Gourmet Variety Pack Cookies - Net Wt. 15 oz UPC 289786003997 Gourmet Variety Pack Cookies Net Wt. 30 oz UPC 289772006995
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0818-2017·2016-12-28

    Fairway Candy Corn Recalled for Undeclared Egg Allergen

    Fairway Market is recalling Candy Corn for potentially containing undeclared egg. The product was sold in New York, New Jersey, Connecticut, and online.

    Product
    FAIRWAY LIKE NO OTHER MARKET brand CANDY CORN, of varying weight, Item Code 228402 XXXXXX -- The product is packaged in clear, plastic cello bags of varying weights, each weighing less than one pound. --- PACKAGED BY FAIRWAY MARKET 2284 12TH AVE., NEW YORK, NY 10027
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0811-2017·2016-12-28

    Medtronic Arrive Braided Transseptal Sheath Recalled for Fragmentation

    Oscor, Inc. is recalling Medtronic Arrive Braided Transseptal Sheaths because a fragment of the inner liner detached during insertion.

    Product
    MEDTRONIC ARRIVE BRAIDED TRANSSEPTAL SHEATH 10F C55¿ S61CM D66CM GLOBAL Catalog # 990061-055-000 Is designed to facilitate the introduction of catheters to any of the heart chambers, including the left atrium via a transseptal puncture.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Food)·F-0753-2017·2016-12-28

    Real Fudge Recalls White Fudge Oreo for Undeclared Wheat and Blue 1

    Real Fudge is recalling White Fudge Oreo products due to undeclared wheat and Blue 1 dye. The recall affects 8 oz. and 16 oz. containers distributed in five states.

    Product
    White Fudge Oreo, brand Real Fudge. Product is sold in clear plastic deli container in 8 oz. and 16 oz.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0812-2017·2016-12-28

    Brownwood Farms Recalls BBQ Mustard Glaze for Undeclared Soy

    Brownwood Farms is recalling BBQ Mustard Glaze because it contains soy ingredients not declared on the label.

    Product
    Brownwood Farms BBQ Mustard Glaze. 11oz glass bottles and 1 gallon. Private labels: Kimmel Orchard & Vineyard (Barbeque Mustard 11oz)
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0877-2017·2016-12-28

    BD SurePath Collection Vials Recalled Due to Cracked Caps

    Becton Dickinson is recalling SurePath collection vials because cracked caps may allow preservative fluid to leak.

    Product
    BD SurePathTM Preservative Collection Vials, catalog numbers 490505, 490527, 491095, 491096, and 491097. SurePath¿ Preservative Fluid is designed for use with the PrepStain¿ System. SurePath¿ Preservative Fluid is an alcohol-based, preservation solution that serves as a trans
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0893-2017·2016-12-28

    Ansell Recalls Gammex Surgical Gloves Due to Latex Contamination

    Ansell Healthcare Products is recalling 15 cases of Gammex Non-Latex Surgical Gloves because they incorrectly contained natural rubber latex gloves.

    Product
    Gammex Non-Latex Sensitive Neoprene Surgical Gloves Ansell Lanka (pvt) Ltd. Biyagama Export Processing Zone, Biyagama, Sri Lanka Ansell Healthcare Europe, N.V Internationaleiaan 55, 1070 Brussels, Belgium Manufactured for/ Fabrique' pour: Ansell Healthcare products LLC.
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Devices)·Z-0808-2017·2016-12-28

    Oscor Medical Sheath Recall Due to Inner Liner Fragmentation During Insertion

    Oscor, Inc. is recalling 33 units of the Adelante Breezway 10F Straight sheath because a fragment of the inner liner detached during insertion.

    Product
    OSCOR ADELANTE BREEZWAY 10F STRAIGHT S79CM D84CM Catalog # AB101219 Is designed to facilitate the introduction of catheters to any of the heart chambers, including the left atrium via a transseptal puncture.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Food)·F-0823-2017·2016-12-28

    Northern Fish Products Recalls Smoked Salmon for Undeclared Soy

    Northern Fish Products is recalling hot smoked salmon, black cod, steelhead, and trout due to undeclared soy.

    Product
    WILD CATCH PREMIUM SMOKED SALMON***NATURAL***NET WT: 4OZ*** UPC 7 02772 00559 6. Cardboard type label is folded over and affixed to the top of the package. Sell by date is marked on the label by the consignee.
    Category
    Food
    Distribution
    5 states
  • HighNHTSA·16V936000·2016-12-28

    Maserati Recalls 2017 Levante S for Engine Software Defect

    Maserati is recalling 2017 Levante S vehicles because engine software may cause the transmission to shift to neutral or the engine to shut down at low speeds.

    Product
    MASERATI — MASERATI LEVANTE S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0774-2017·2016-12-28

    Wakefern Recalls Gourmet Variety Pack Cookies Due to Metal Pieces

    Wakefern Food Corp. is recalling specific varieties of gourmet cookies because they may contain metal pieces.

    Product
    12PK Gourmet Variety Pack Cookies 15 Oz.. UPC 289786203991 24 pack Variety Cookies Net Wt. 24 oz. UPC 208726004191
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0778-2017·2016-12-28

    Wakefern Take&Bake Oatmeal Raisin Cookies Recalled for Metal Pieces

    Wakefern Food Corp. is recalling 24-count Take&Bake Oatmeal Raisin Cookies because they may contain metal pieces. The product was distributed in six states.

    Product
    24CT Take&Bake Oatmeal Rasin Cookies Net Wt. 24oz UPC 20873004194
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0822-2017·2016-12-28

    Northern Fish Products Recalls Smoked Salmon for Undeclared Soy

    Northern Fish Products is recalling hot smoked salmon, black cod, steelhead, and trout due to undeclared soy. Hot jerky salmon and jerky salmon are excluded.

    Product
    "***PREMIUM SMOKED SALMON***CRACKED PEPPER*** NET WT: 4OZ***Packaged 5 lbs case 20/4oz vacuum packages/case. Cardboard type label is folded over and affixed to the top of the package. Sell by date is marked on the label by the consignee. UPC 7 02772 00560 2.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-0865-2017·2016-12-28

    Accuray Recalls CyberKnife Robotic Radiosurgery Systems Due to Electric Shock Risk

    Accuray is recalling 115 CyberKnife Robotic Radiosurgery Systems (models G3, G4, VSI) due to a potential electric shock hazard during maintenance.

    Product
    CyberKnife Robotic Radiosurgery Systems, models: G3, G4, VSI. Radiology: The CyberKnife Robotic Radiosurgery System is indicated for treatment planning and image guided stereotactic Radiosurgery and precision radiotherapy for lesions, tumors and conditions anywhere in the body
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-0812-2017·2016-12-28

    Medtronic Arrive Braided Transseptal Sheath Recalled for Inner Liner Fragmentation

    Oscor, Inc. is recalling Medtronic Arrive Braided Transseptal Sheaths because an inner liner fragment was found during insertion. The recall covers 1,729 units distributed worldwide.

    Product
    MEDTRONIC ARRIVE BRAIDED TRANSSEPTAL SHEATH 10F C70¿ S61CM D66CM GLOBAL Catalog # 990061-070-000 Is designed to facilitate the introduction of catheters to any of the heart chambers, including the left atrium via a transseptal puncture.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0777-2017·2016-12-28

    AngioDynamics Recalls Stiffened Micro-Introducer Kits Due to Detachment Risk

    AngioDynamics is recalling 7 boxes of Stiffened Micro-Introducer Kits because the rotating luer on the included sheath/dilator components may detach from the hub during use.

    Product
    ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5 F Stiffened Micro-Introducer Kit, 45CM NT/T NON-ECHO B PG, Item Number H787065970685, Catalog No.REF 06597068, 2) 1) 5 F Stiffened Micro-Introducer Kit, 45CM NT/T NON-ECHO S PG, Item Number H787065970705,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0806-2017·2016-12-28

    Crescent Vending Recalls Hot Sicilian Sandwiches for Undeclared Allergens

    Crescent Vending Co. Inc. is recalling Hot Sicilian sandwiches due to undeclared wheat, soy, and milk allergens.

    Product
    Hot Sicilian- Ham, Pepperoni and Provolone Cheese wrapped in clear film, 5 oz. Undeclared allergens - Wheat, Soy( oil flour), Milk
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0799-2017·2016-12-28

    Crescent Vending Recalls Chicken Salad Sandwiches for Undeclared Allergens

    Crescent Vending Co. Inc. is recalling 20 chicken salad sandwiches on Kaiser rolls in Pennsylvania due to undeclared wheat, soy, and milk allergens.

    Product
    Chicken Salad on Kaiser Roll, 5 oz. Undeclared allergens - Wheat, Soy (oil, flour)
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0782-2017·2016-12-28

    Wakefern Recalls Oatmeal Raisin Cookies Due to Metal Pieces

    Wakefern Food Corp. is recalling 24-count oatmeal raisin cookies because they may contain metal pieces. The product was distributed in six states.

    Product
    24CT Oatmeal Raisin Cookies Net Wt. 24oz UPC 208710004190
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0891-2017·2016-12-28

    Amendia Recalls Optimus Fixed Awl Due to Tip Breakage During Surgery

    Amendia, Inc. is recalling nine Optimus Fixed Awl devices because the tip broke after impaction during surgery. The devices were distributed to Florida, Georgia, Illinois, Missouri, and Texas.

    Product
    Optimus Fixed Awl
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Devices)·Z-0817-2017·2016-12-28

    Oscor Recalls Medtronic Arrive Braided Transseptal Sheaths Due to Liner Fragmentation

    Oscor, Inc. is recalling 991 units of Medtronic Arrive Braided Transseptal Sheaths because a fragment of the inner liner detached during insertion.

    Product
    MEDTRONIC ARRIVE BRAIDED TRANSSEPTAL SHEATH 10F C90¿ S79CM D84CM GLOBAL Catalog # 990079-090-000 Is designed to facilitate the introduction of catheters to any of the heart chambers, including the left atrium via a transseptal puncture.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0809-2017·2016-12-28

    Oscor Medical Sheath Recall Due to Inner Liner Fragmentation

    Oscor, Inc. is recalling 20 units of the Adelante Breezeway sheath because a fragment of the inner liner detached during insertion.

    Product
    OSCOR ADELANTE BREEZEWAY 10F STRAIGHT S61CM D66CM Catalog # AB10218 Is designed to facilitate the introduction of catheters to any of the heart chambers, including the left atrium via a transseptal puncture.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0790-2017·2016-12-28

    Oscor Medical Sheath Recall Due to Inner Liner Fragmentation

    Oscor, Inc. is recalling 156 units of the Adelante Breezeway sheath because a fragment of the inner liner detached during insertion.

    Product
    OSCOR ADELANTE BREEZEWAY 8F C55¿ S61CM D66CM Catalog # AB081040 Is designed to facilitate the introduction of catheters to any of the heart chambers, including the left atrium via a transseptal puncture.
    Category
    Medical Device
    Distribution
    8 states
  • HighNHTSA·16V938000·2016-12-28

    Navistar Recalls 2017 International Trucks Due to Battery Latch Fire Risk

    Navistar is recalling 2017 International ProStar, LoneStar, 9900i, and TranStar trucks because a battery latch may cause an electrical short and fire.

    Product
    INTERNATIONAL — INTERNATIONAL PROSTAR, LONESTAR, 9900I, TRANSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0816-2017·2016-12-28

    Medtronic Arrive Braided Transseptal Sheath Recalled for Liner Fragmentation

    Oscor, Inc. is recalling Medtronic Arrive Braided Transseptal Sheaths because a fragment of the inner liner may come out during insertion.

    Product
    MEDTRONIC ARRIVE BRAIDED TRANSSEPTAL SHEATH 10F C70¿ S79CM D84CM GLOBAL Catalog # 990079-070-000 Is designed to facilitate the introduction of catheters to any of the heart chambers, including the left atrium via a transseptal puncture.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Food)·F-0802-2017·2016-12-28

    Crescent Vending Recalls Sandwiches with Undeclared Allergens

    Crescent Vending Co. Inc. is recalling 13 meatball sandwiches for failing to declare wheat, soy, and milk allergens.

    Product
    Meatball on an Italian Roll with Cole Slaw wrapped in clear film, 8 oz. Undeclared allergens - Wheat, Soy (oil, flour), Milk, Egg
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0944-2017·2016-12-28

    Ariels OM Grown Granola Recalled for Wheat Seed Contamination

    Hummingbird Wholesale is recalling Ariels OM Grown Granola because it was contaminated with wheat seed. The product was distributed in California, Oregon, and Washington.

    Product
    Ariels OM Grown Granola. Product number GR200, net wt. 5 lb., packaged in bulk bag inside plastic bucket. Product number GR201, net wt.15 lb., packaged in bulk bag inside plastic bucket. Product number BAG-GR200, net wt. 8 oz., packaged in cellophane bag with cardstock label
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0809-2017·2016-12-28

    Crescent Vending Recalls Salisbury Steak Sandwiches for Undeclared Allergens

    Crescent Vending Co. Inc. is recalling 8-ounce Salisbury Steak sandwiches with gravy and whipped potatoes because they contain undeclared wheat, soy, and milk.

    Product
    Salisbury Steak with Gravy on Kaiser with whipped potatoes wrapped in clear film, 8 oz. Undeclared allergens - Wheat, Soy (oil, flour), Milk
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0807-2017·2016-12-28

    Oscor Medical Sheath Recalled Due to Inner Liner Fragmentation

    Oscor, Inc. is recalling 34 units of the Adelante Breezeway 10F Straight sheath because a fragment of the inner liner detached during insertion.

    Product
    OSCOR ADELANTE BREEZEWAY 10F STRAIGHT S61CM D66CM Catalog # AB101218 Is designed to facilitate the introduction of catheters to any of the heart chambers, including the left atrium via a transseptal puncture.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Food)·F-0945-2017·2016-12-28

    Streit's Quinoa with Mushrooms Recalled for Undeclared Sulfites

    Aron Streit Inc is recalling Streit's Quinoa with Mushrooms & Herbs due to the presence of undeclared sulfites.

    Product
    Streit's Quinoa with Mushrooms & Herbs, Net Wt. 7.7 oz (220g). Product of Israel
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0828-2017·2016-12-28

    Northern Fish Products Recalls Hot Smoked Salmon Due to Undeclared Soy

    Northern Fish Products is recalling hot smoked salmon, black cod, steelhead, and trout because they contain undeclared soy.

    Product
    Kippered Salmon Tips Product of USA Packed By Northern Fish Products***" Packaged in bulk 5lb case.
    Category
    Food
    Distribution
    5 states

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