The Recall Desk

Archive

July 2017 recalls

930 recalls were announced in July 2017.

What the numbers show

Critical
40
Severe
116
High
613
Moderate
135
Low
26

Of the 930 recalls this month scored against our rubric, 4% are Critical, 12% are Severe.

701–800 of 930

  • ModerateFDA (Food)·F-2583-2017·2017-07-19

    Lyrical Foods Recalls Kite Hill Almond Yogurt Due to Spoilage

    Lyrical Foods is voluntarily recalling Kite Hill Almond Yogurt because some packages spoiled before the best-by date.

    Product
    Kite Hill Almond Yogurt, Blueberry , NET WT. 5.3 oz (150G) Case UPC: 8-56624-00413-5 Distributed by Lyrical Foods, Hayward, CA.
    Category
    Food
    Distribution
    15 states
  • ModerateFDA (Food)·F-2464-2017·2017-07-19

    3CS Organics Recalls HIPP Organic Infant Milk Products for Labeling Issues

    3CS Organics is recalling HIPP Organic infant milk products because they are not FDA approved and lack full English labeling.

    Product
    HIPP Organic Comb Hungry Infant Milk, 800g (4bx/case), HIPP Organic Comb First Infant Milk, 800g (4bx/case), HIPP Organic Combiotic Follow on Milk 2, 800g (4bx/case), HIPP Organic Good Night Milk from 6 Months, 350g (12cans/case)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2708-2017·2017-07-19

    Toshiba XARIO 100 Ultrasound Systems Recalled for Incorrect Velocity Readings

    Toshiba American Medical Systems is recalling seven XARIO 100 diagnostic ultrasound systems because they may display incorrect values when using the Continuous Trace method for velocity measurements.

    Product
    XARIO 100 TUS-X100 diagnostic ultrasound system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2477-2017·2017-07-19

    Frozen Ginger Snap Cookies Recalled for Chemical Contamination

    Correctional Industries Food Factory is recalling frozen ginger snap cookies made with water contaminated with PFOA and PFOS chemicals.

    Product
    Item 10120 - GINGER SNAP COOKIES, I/W, 2-PK>100-CT/CS, Frozen, Net Wt. 13.89 lbs. per case.
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-2508-2017·2017-07-19

    Frozen Vegan Breakfast Trays Recalled for Chemical Contamination

    Correctional Industries Food Factory is recalling frozen vegan breakfast trays because they were made with water contaminated with PFOA and PFOS chemicals.

    Product
    Item 11930 - VEGAN BREAKFAST TRAY H>36 TRAYS/CS, Frozen, Net. Wt. 33.78 lbs. per case
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-2380-2017·2017-07-19

    Source Naturals Hydrogen Boost Capsules Recalled for Undeclared Boron

    Source Naturals Hydrogen Boost Capsules are being recalled because they contain low levels of undeclared boron. The recall covers 55,354 units distributed nationwide.

    Product
    Source Naturals Hydrogen Boost Capsule: 6 Count Trial, 30 Count, 60 Count; Ingredient: Maltodextrin, Cellulose (Capsules, Silica and magnesium stearate; 30 count Bottle - Product SN1855: 60 count Bottle - Product SN1856; 6 count Bottle - Product SN2314; 30 count + 30
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2582-2017·2017-07-19

    Lyrical Foods Recalls Kite Hill Almond Yogurt Due to Spoilage

    Lyrical Foods is voluntarily recalling Kite Hill Almond Yogurt because some packages spoiled before the best by date.

    Product
    Kite Hill Almond Yogurt, Pineapple, NET WT. 5.3 oz (150G) Case UPC: 8-56624-00435-7 Distributed by Lyrical Foods, Hayward, CA.
    Category
    Food
    Distribution
    15 states
  • ModerateFDA (Food)·F-2478-2017·2017-07-19

    Frozen Chocolate Chip Cookies Recalled for Chemical Contamination

    Correctional Industries Food Factory is recalling frozen chocolate chip cookies made with water contaminated by PFOA and PFOS chemicals.

    Product
    Item 10132 - CHOCOLATE CHIP COOKIES, I/W, 2-PK>100-CT/CS, Frozen, Net Wt. 13.89 lbs. per case.
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-2520-2017·2017-07-19

    Frozen Bean and Cheese Burritos Recalled for Chemical Contamination

    Correctional Industries Food Factory is recalling frozen bean and cheese burritos because they were made with water contaminated with PFOA and PFOS.

    Product
    Item 12788 - BEAN AND CHEESE BURRITO WITH RICE AND CORN>24EA/CS, Frozen, Net. Wt. 25.43 lbs. per case
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-2521-2017·2017-07-19

    Correctional Industries Recalls Vegan Chili Contaminated with PFOA and PFOS Chemicals

    Correctional Industries Food Factory is recalling frozen vegan chili with rice and vegetables because it was made with water contaminated with PFOA and PFOS chemicals.

    Product
    Item 14600 - VEGAN CHILI WITH RICE AND VEGETABLES>24EA/CS, Frozen, Net. Wt. 22.99 lbs. per case
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-2397-2017·2017-07-19

    Dawn's Foods Tropical Fruit Dip Recalled for Undeclared Yellow #5

    Morski Brands, Inc. is recalling Dawn's Foods Tropical Fruit Dip in Wisconsin due to undeclared Yellow #5 dye.

    Product
    Dawn's Foods Tropical Fruit Dip. Nwt WT. 4 lbs. (1.82Kg) Keep Refrigerated. For Foodservice Use only.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-2516-2017·2017-07-19

    Frozen Cheesy Egg Omelet Recalled for Chemical Contamination

    Correctional Industries Food Factory is recalling frozen Cheesy Egg Omelets because they were made with water contaminated with PFOA and PFOS chemicals.

    Product
    Item 12730 - CHEESY EGG OMELET WITH SWEET RICE AND O'BRIEN POTATOES>24EA/CS, Frozen, Net. Wt. 19.19 lbs. per case
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-2481-2017·2017-07-19

    Frozen PB&J Snacks Recalled for Chemical Contamination in Water

    Correctional Industries Food Factory is recalling frozen PB&J snacks made with water contaminated by PFOA and PFOS chemicals.

    Product
    Item 10232 - YELLOW (PB&J) SNACK>50-CT/CS, Frozen, Net Wt. 16.12 lbs. per case.
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-2497-2017·2017-07-19

    Frozen Breakfast Muffins Recalled for Chemical Contamination in Water

    Correctional Industries Food Factory is recalling frozen breakfast muffins made with water contaminated with PFOA and PFOS chemicals exceeding EPA health advisory levels.

    Product
    Item 10554- BREAKFAST MUFFINS, I/W>50-CT/CS, Frozen, Net Wt. 17.3 lbs. per case.
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-2469-2017·2017-07-19

    3CS Organics Recalls Topfer Lactana Bio Infant Formula for Labeling Issues

    3CS Organics LLC is recalling Topfer Lactana Bio infant and follow-up formula because the product is not FDA approved and lacks complete English labeling.

    Product
    Topfer Lactana Bio 1 Anfangsmilch, 600g (3/case), Topfer Lactana Bio 2, Bio Folgemilch, 600g (3bx/case)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2523-2017·2017-07-19

    Frozen Vegan Sloppy Joe Meal Recalled for Chemical Contamination

    Correctional Industries Food Factory is recalling frozen vegan sloppy joe meals because they were made with water contaminated with PFOA and PFOS chemicals.

    Product
    Item 14604 - VEGAN SLOPPY JOE, TATOR PUFFS AND VEGETABLES>24EA/CS, Frozen, Net. Wt. 26.89 lbs. per case
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-2531-2017·2017-07-19

    Frozen Vegan Bean Burritos Recalled for Chemical Contamination

    Correctional Industries Food Factory is recalling frozen vegan bean burritos because they were made with water contaminated with PFOA and PFOS chemicals.

    Product
    Item 14622 - VEGAN SPICY BEAN BURRITO WITH RED CHILI SAUCE, RICE AND VEGETABLES>24EA/CS, Frozen, Net. Wt. 28.43 lbs. per case
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-2467-2017·2017-07-19

    HOLLE Organic Infant Formula Recalled for Lack of FDA Approval

    3CS Organics LLC is recalling HOLLE organic infant formula products because they are not FDA approved and lack English labeling.

    Product
    HOLLE Bio Zulgelingen Opvolgmelk 2, (3/case), HOLLE Bio Lait de suite, 2, 400g (6/case), HOLLE Bio Lait pour Nourrissons Zulgelingenmelk, 400g (6/case), HOLLE Lait Pour Nourrissons 1er Age Bio, 400g (6/case). HOLLE Bio Lait de Suit Au Lait De Chevre, 400g (6/case) , HOLLE Bio-Ki
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2474-2017·2017-07-19

    Frozen Turkey Ham Lunch Recalled for Chemical Contamination

    Correctional Industries Food Factory is recalling frozen turkey ham lunch trays made with water contaminated with PFOA and PFOS chemicals.

    Product
    Item 11952 - TURKEY HAM LUNCH>36 TRAYS/CS, Frozen, Net. Wt. 24.76 lbs.
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-2529-2017·2017-07-19

    Correctional Industries Recalls Vegan Navy Bean Hash Due to Chemical Contamination

    Correctional Industries Food Factory is recalling frozen Vegan Navy Bean Hash and Sweet Rice with Raisins because it was made with water contaminated with PFOA and PFOS.

    Product
    Item 14618 - VEGAN NAVY BEAN HASH AND SWEET RICE WITH RAISINS>24EA/CS, Frozen, Net. Wt. 29.56 lbs. per case
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-2730-2017·2017-07-19

    Beckman Coulter Synchron AQUA CAL Level 1 Calibration Kits Recalled

    Beckman Coulter is recalling Synchron AQUA CAL Level 1 kits due to a sodium recovery shift that may affect system calibration.

    Product
    Beckman Coulter Synchron AQUA CAL Level 1, Part No. 471288 Product Usage: Used for the system calibration of Na, K, Cl, Urea N, Urea, Glucose Creatine, Ca, CO2, and P in UniCel DxC Systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2725-2017·2017-07-19

    AMS Diagnostics Recalls Medica ISE Module Calibrant A Due to Physical Defects

    AMS Diagnostics is recalling 9 units of Medica ISE Module Calibrant A because the lot was not functioning properly and did not exhibit correct physical properties.

    Product
    Medica ISE Module Calibrant A; 500 mL - 140 mmol/L Na+, 125 mmol/L Cl-, buffers and preservatives; For use with ISE Module; Product Usage: Calibrations of ISE Model for integrated electrolyte system analysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V457000·2017-07-18

    Mazda Recalls CX-7, CX-9, and Mazda6 for Air Bag Inflator Rupture Risk

    Mazda is recalling specific 2007-2012 CX-7, CX-9, and Mazda6 vehicles because the passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.

    Product
    MAZDA — MAZDA CX-9, CX-7, MAZDA6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E038000·2017-07-18

    TriMark Recalls Ambulance Door Striker Bolts for Crash Safety Non-Compliance

    TriMark is recalling specific door striker bolts used in ambulance door systems because they may fail during a crash, causing doors to open and increasing injury risk.

    Product
    STRUCTURE:BODY:DOOR:HINGE AND ATTACHMENTS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17756·2017-07-18

    Polaris Recalls RZR 570 and RZR S 570 Off-Highway Vehicles

    Polaris is recalling about 1,160 RZR 570 and RZR S 570 vehicles because the front brake can detach, posing crash and injury hazards.

    Product
    Polaris RZR 570 and RZR S 570 recreational off-highway vehicles (ROVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V456000·2017-07-18

    Winnebago Recalls 2015 Transit Buses for Weight Rating Compliance Issues

    Winnebago is recalling 2015 Transit Bus 28SH and 28WC models because they may exceed weight ratings when fully loaded, increasing crash risk.

    Product
    WINNEBAGO — WINNEBAGO TRANSIT BUS28SH, TRANSIT BUS28WC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V455000·2017-07-18

    Pierce Fire Trucks Recalled for Water Pump Interlock Failure

    Pierce is recalling 2016-2017 fire trucks because a pressure switch may fail in extreme cold, preventing the water pump from operating.

    Product
    PIERCE — PIERCE ENFORCER, VELOCITY, QUANTUM, ARROW XT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V454000·2017-07-17

    Thomas Built Buses Saf-T-Liner C2 Recalled for Wheelchair Anchorage Defect

    Daimler Trucks North America is recalling 2005-2018 Thomas Built Buses Saf-T-Liner C2 transit buses because the wheelchair pocket track anchorage may not secure a wheelchair in a crash.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V451000·2017-07-17

    Freightliner Custom Chassis XCR Recalled for Battery Cable Fire Risk

    Daimler Trucks North America is recalling 2014-2017 Freightliner Custom Chassis XCR vehicles because an improperly installed battery cable bracket may cause a short circuit and fire.

    Product
    FCCC — FCCC, FREIGHTLINER CUSTOM CHASS XCR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17E037000·2017-07-17

    PACCAR Recalls Braden Hydraulic Recovery Winches Due to Adapter Defect

    PACCAR is recalling specific Braden Hydraulic Recovery winches because a defective ring gear adapter may cause failure under load, posing an injury risk.

    Product
    EQUIPMENT:MECHANICAL:WINCH recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V452000·2017-07-17

    Daimler Trucks Recalls 2018 Freightliner and Western Star Models for Tow Hook Defect

    Daimler Trucks North America is recalling 2,483 2018 Freightliner and Western Star trucks because their tow hooks may fail during recovery operations, increasing the risk of injury.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR M2 BUSINESS CLASS, 122SD, CASCADIA, 114SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V453000·2017-07-17

    Thomas Built Buses Recalls Saf-T-Liner C2 School Buses for Wheelchair Defect

    Daimler Trucks North America is recalling 2005-2018 Thomas Built Buses Saf-T-Liner C2 school buses because wheelchair pocket track anchorages may not secure wheelchairs in a crash.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V448000·2017-07-16

    Smart Fortwo Recall for Parking Brake Cable Lock Nut Issue

    Mercedes-Benz USA is recalling 2016 Smart Fortwo vehicles because the parking brake cable lock nut may loosen, potentially reducing the vehicle's ability to stay secured on slopes.

    Product
    SMART — SMART FORTWO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·082-2017·2017-07-15

    Marathon Enterprises Recalls Hot Dogs Due to Bone Fragment Contamination

    Marathon Enterprises is recalling approximately 7.2 million pounds of hot dog products due to potential bone fragment contamination. One minor oral injury has been reported.

    Product
    Marathon Enterprises Inc. — Marathon Enterprises Inc. Recalls Hot Dog Products Due to Possible Extranous Material Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V444000·2017-07-14

    Keystone Recalls 2016-2018 Avalanche Trailers Due to Tire Hazard

    Keystone RV Company is recalling 2016-2018 Avalanche recreational trailers because a kitchen slide-out bolt could contact the front tire, potentially causing sudden tire failure and increasing crash risk.

    Product
    KEYSTONE — KEYSTONE AVALANCHE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V447000·2017-07-14

    Mercedes-Benz Recalls 2017 Smart Fortwo Vehicles for Steering Knuckle Defect

    Mercedes-Benz USA is recalling 2017 Smart Fortwo and Cabriolet vehicles because casting imperfections in the left front axle steering knuckle could cause failure and increase crash risk.

    Product
    SMART — SMART FORTWO, FORTWO CABRIOLET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·081-2017·2017-07-14

    Custom Culinary Recalls Chicken and Beef Soup Bases Due to Misbranding

    Custom Culinary, Inc. is recalling approximately 9,444 pounds of chicken and beef soup base products due to misbranding and undeclared soy allergens.

    Product
    Custom Culinary, Inc. — Custom Culinary, Inc. Recalls Chicken and Beef Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • LowNHTSA·17V445000·2017-07-14

    Forest River Recalls 2017 Rockwood Travel Trailers for VIN Label Error

    Forest River is recalling 2017 Rockwood travel trailers because an incorrect check digit on the VIN label may hinder vehicle registration and safety recall tracking.

    Product
    FOREST RIVER — FOREST RIVER ROCKWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17187·2017-07-13

    TJX Recalls Glass Beer Mugs Due to Burn and Laceration Hazards

    TJX is recalling glass beer mugs sold at HomeGoods because they can break when heated or used with hot liquids, posing burn and laceration risks.

    Product
    Glass beer mugs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17186·2017-07-13

    YSN Imports Recalls Refillable Propane Cylinders Due to Fire and Explosion Hazards

    YSN Imports is recalling approximately 24,000 refillable propane cylinders sold under Flame King, Little Kamper, and U-Haul brands because the connecting valve can unscrew, posing fire and explosion risks.

    Product
    Refillable propane cylinders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V440000·2017-07-13

    Jayco Recalls 2017 Jay Flight SLX Trailers for Inaccurate Weight Labels

    Jayco is recalling 2017 Jay Flight SLX travel trailers with the Rocky Mountain Package because their cargo capacity labels are inaccurate, which could lead to overloading.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER JAY FLIGHT SLX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V441000·2017-07-13

    Entegra Recalls 2018 Cornerstone Motorhomes Due to Fuel Pump Defect

    Entegra is recalling 18 units of 2018 Cornerstone motorhomes because a fuel pump drive gear could slip, causing engine stalls and increasing crash risk.

    Product
    ENTEGRA — ENTEGRA CORNERSTONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V443000·2017-07-13

    PACCAR Recalls Peterbilt and Kenworth Trucks Due to Fuel Pump Defect

    PACCAR is recalling 2017-2018 Peterbilt and 2018 Kenworth trucks equipped with Cummins ISX 15L engines because a fuel pump drive gear could slip, causing an engine stall.

    Product
    PETERBILT — PETERBILT, KENWORTH 367, 567, 579, 587
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2438-2017·2017-07-12

    Bulletproof Lemon Cookie Collagen Protein Bar Recalled for Listeria Risk

    Bulletproof 360 Inc is recalling Lemon Cookie Collagen Protein Bars due to potential Listeria monocytogenes contamination. The recall covers specific lots sold nationwide and internationally.

    Product
    Lemon Cookie Collagen Protein Bar. Each Bar is packed in foil wrapper, net wt. per Bar is 1.58 oz (45g). There 12 bars packed in a box and the net wt. is 18.96 oz (540g). Individual Bar UPC 815709021801. Box UPC 815709021795.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2440-2017·2017-07-12

    Bulletproof Recalls Vanilla Shortbread Collagen Protein Bites for Listeria Risk

    Bulletproof 360 Inc is recalling Vanilla Shortbread Collagen Protein Bites due to potential Listeria monocytogenes contamination. The recall covers specific lots distributed nationwide and internationally.

    Product
    Vanilla Shortbread Collagen Protein Bite. Each Bite is packed in foil wrapper, net wt. per Bar is 0.74 oz (21g). There 15 pieces packed in a box and the net wt. is 11.10 oz (315 g). Individual Bar UPC 815709021504. Box UPC 815709021511.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2439-2017·2017-07-12

    Bulletproof Vanilla Shortbread Collagen Protein Bar Recalled for Listeria Risk

    Bulletproof 360 Inc is recalling Vanilla Shortbread Collagen Protein Bars due to potential Listeria monocytogenes contamination. The recall covers specific lots distributed nationwide and internationally.

    Product
    Vanilla Shortbread Collagen Protein Bar. Each Bar is packed in foil wrapper, net wt. per Bar is 1.58 oz (45g). There 12 bars packed in a box and the net wt. is 18.96 oz (540g). Individual Bar UPC 815709021481. Box UPC 815709020804.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2417-2017·2017-07-12

    Eatem Foods Recalls South African Style Spice Paste Due to Peanut Allergen

    Eatem Foods is recalling 10,650 pounds of South African Style Perl Perl Roasted Spice Paste because a supplier detected peanut allergen in an ingredient.

    Product
    SOUTH AFRICAN STYLE PERl PERl ROASTED SPICE PASTE INGREDIENTS: VINEGAR, JALAPENO PUR E;(jalapeno peppers, salt, vinegar), ONION, MINCED GARLIC (garlic, soybean oil, citric acid),PAPRIKA, CANOLA OIL, GRANULATED ONION, BIRDS EYE CHILl PEPPER, SALT,LEMON JUICE CONCENTRATE,SPICE
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-2437-2017·2017-07-12

    Bulletproof Fudge Brownie Collagen Protein Bites Recalled for Listeria Risk

    Bulletproof 360 Inc is recalling Fudge Brownie Collagen Protein Bites due to potential Listeria monocytogenes contamination. The recall covers products sold nationwide and internationally.

    Product
    Fudge Brownie Collagen Protein Bite. Each Bite is packed in foil wrapper, net wt. per Bite 0.74 oz (21g). There 15 pieces packed in a box and the net wt. is 11.10 oz (315 g). Individual Bar UPC 815709021528. Box UPC 815709021535.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0939-2017·2017-07-12

    Alvogen Recalls Clindamycin Injection Vials Due to Sterility Concerns

    Alvogen, Inc. is recalling 5,100 vials of Clindamycin Injection USP due to a lack of assurance of sterility. The affected product was distributed nationwide.

    Product
    Clindamycin Injection USP; 300 mg/2 mL (150 mg/mL). 2 mL Single-dose ADD-VANTAGE Vial, Rx Only, Manufactured for Alvogen, Inc., Pine Brook, NJ 07058, NDC 47781-462-69
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0946-2017·2017-07-12

    Fagron Recalls Succinylcholine Chloride Syringes Due to Sterility Concerns

    Fagron Compounding Services is voluntarily recalling 1,056 syringes of Succinylcholine Chloride because the company cannot ensure the product is sterile.

    Product
    Succinylcholine Chloride, 100 mg per 5mL, 20 mg per mL syringe. IV Use Only. JCB Laboratories, 8710 E 34th St., N. Wichita, KS 67226 UPC 7335968405
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2436-2017·2017-07-12

    Bulletproof Fudge Brownie Collagen Protein Bar Recalled for Listeria Risk

    Bulletproof 360 Inc is recalling Fudge Brownie Collagen Protein Bars due to potential Listeria monocytogenes contamination.

    Product
    Fudge Brownie Collagen Protein Bar. Each bar is packed in foil wrapper, net wt. per bar 1.58 oz (45g). There 12 bars packed in a box and the net wt. per box is 18.96 oz (540g). Individual Bar UPC 815709021498. Box UPC 815709020811.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2425-2017·2017-07-12

    Smucker Foods Recalls Golden Temple Atta Flour Due to E. coli Risk

    Smucker Foods of Canada Co. is recalling Golden Temple No. 1 Fine Durum Atta Flour Blend because it may be contaminated with E. coli.

    Product
    Golden Temple No. 1 Fine Durum Atta Flour Blend NET WT 20 LB INGREDIENTS: DURUM WHEAT FLOUR, DURUM WHEAT BRAN, WHEAT FLOUR, NIACIN, REDUCED IRON, THIAMIN MONONITRATE, RIBOFLAVIN, FOLIC ACID. DISTRIBUTED BY: SMUCKER FOODS OF CANADA CORP., MARKHAM, ON L3R 0P3 PRODUCT OF CANADA UPC
    Category
    Food
    Distribution
    13 states
  • SevereFDA (Food)·F-2424-2017·2017-07-12

    Smucker Foods Recalls Durum Atta Flour for Potential E. coli Contamination

    Smucker Foods of Canada Co. is recalling specific brands of Durum Atta Flour due to potential E. coli contamination reported by a co-packer.

    Product
    Flour sold under the following brands: Golden Temple Durum Atta Flour Blend, 20LB, DISTRIBUTED BY: SMUCKER FOODS OF CANADA CORP., MARKHAM, ON L3R 0P3 PRODUCT OF CANADA UPC 0 59000 41556 7, Swad Durum Atta Flour, 20 LB MILLED FOR: RAJA FOODS 8110 N. St. Louis Avenue Skokie, IL 600
    Category
    Food
    Distribution
    13 states
  • SevereFDA (Drugs)·D-0940-2017·2017-07-12

    Alvogen Recalls Clindamycin Injection Vials Due to Sterility Concerns

    Alvogen, Inc. is recalling 72,575 vials of Clindamycin Injection USP due to a lack of assurance of sterility. The affected lots were distributed nationwide.

    Product
    Clindamycin Injection USP; 600 mg/4 mL (150 mg/mL). 4 mL Single-dose ADD-VANTAGE Vial, Rx Only, Manufactured for Alvogen, Inc., Pine Brook, NJ 07058, NDC 47781-463-69
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0948-2017·2017-07-12

    TetraStem Topical Antibiotic Ointment Recalled for Manufacturing Deviations

    Phillips Co. is recalling TetraStem Topical Ointment First Aid Antibiotic because FDA inspections found significant manufacturing deviations that raise questions about product safety and quality.

    Product
    TetraStem brand Topical Ointment First Aid Antibiotic, tetracycline (3%), 3 mL in a 5 mL bottle, sold over the counter Phillips Company, Millerton, OK -- NDC 04307-301-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0950-2017·2017-07-12

    Phillips Co. Recalls StingMed Insect Bites Skin Protectant Due to GMP Deviations

    Phillips Co. is recalling StingMed Insect Bites Skin Protectant because FDA inspections found significant manufacturing deviations that raise questions about the product's safety and quality.

    Product
    StingMed Insect bites Skin Protectant. Zinc acetate (.1% by volume), 0.3 fl. oz. (3 mL) bottle, Phillips Company, Millerton, OK -- NDC 04307-100-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0941-2017·2017-07-12

    Alvogen Recalls Clindamycin Injection Vials Due to Sterility Concerns

    Alvogen, Inc. is recalling specific lots of Clindamycin Injection USP due to a lack of assurance of sterility. The recall covers 71,825 vials distributed nationwide.

    Product
    Clindamycin Injection USP; 900 mg/6 mL (150 mg/mL). 6 mL Single-dose ADD-VANTAGE Vial, Rx Only, Manufactured for Alvogen, Inc., Pine Brook, NJ 07058, NDC 47781-464-69
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0951-2017·2017-07-12

    Phillips Recalls StaphWash Skin Protectant Due to Manufacturing Deviations

    Phillips Co. is recalling StaphWash+Plus+ Skin Protectant because FDA inspections found manufacturing practices that question the product's safety and quality.

    Product
    StaphWash+Plus+ Skin Protectant, Zinc acetate (.1% by volume), 0.3 fl. oz. (3 mL) bottle, Phillips Company, Millerton, OK -- NDC 43074-101-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0949-2017·2017-07-12

    Phillips Recalls Diabecline Topical Ointment Due to Manufacturing Deviations

    Phillips Co. is recalling Diabecline brand Topical Ointment First Aid Antibiotic because FDA inspections found significant manufacturing deviations that question the product's safety and quality.

    Product
    Diabecline brand Topical Ointment First Aid Antibiotic, tetracycline (3%), 3 mL in a 5 mL bottle, sold over the counter Phillips Company, Millerton, OK -- NDC 04307-100-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0947-2017·2017-07-12

    Phillips Tetracycline Ointment Recalled for Manufacturing Quality Concerns

    Phillips Co. is recalling Tetracycline-ABC Brand Topical Ointment because FDA inspections found significant manufacturing deviations that raise questions about product safety and quality.

    Product
    Tetracycline-ABC Brand Topical ointment First Aid Antibiotic, tetracycline (3%), 3 mL in a 5 mL bottle, sold over the counter Phillips Company, Millerton, OK -- NDC 4307410201
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0952-2017·2017-07-12

    Phillips Co. Recalls VenomX Zinc Acetate Skin Protectant Due to GMP Deviations

    Phillips Co. is recalling VenomX Zinc Acetate Skin Protectant because FDA inspections found manufacturing practices that question the product's safety and quality.

    Product
    VenomX, Zinc acetate (.1% by volume), 0.3 fl. oz. (3 mL) bottles, Skin Protectant Phillips Company, Millerton, OK -- NDC 43074-207-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2657-2017·2017-07-12

    CardioTek EP-TRACER Software Recalled for Unintentional Parameter Changes

    CardioTek BV is recalling EP-TRACER Software V1.x and V2.0 due to a bug that allows parameters to be changed unintentionally during use.

    Product
    CardioTek EP-TRACER Software V1.x and V2.0 The EP-TRACER System is an electrophysiology measurement system used to acquire, filter, digitize, amplify, display, and record signals obtained during electrophysiological studies and related procedures. The system allows the user to
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2670-2017·2017-07-12

    Smiths Medical Recalls Hypodermic Needles Due to Syringe Hub Defects

    Smiths Medical is recalling specific lots of Jelco Hypodermic Needle Pro needles because syringe assemblies used in their manufacture contained pin holes in the hub.

    Product
    Jelco, Hypodermic needle Pro¿ needles 19G X1 1/2" 800/CA Model No. EL 1915 & 19G X 2" 600/CA Model No. SB 5021, Rx Only, Sterile EO.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Food)·F-2420-2017·2017-07-12

    Bacalafoods Recalls Finola Style Octopus Due to Squid Mislabeling

    Bacalafoods Corp is recalling Finola Style Octopus in Pickled Sauce because the product contains squid instead of octopus. The recall covers 203 boxes distributed in Puerto Rico.

    Product
    Finola, Style Octopus in Pickled Sauce, Product of Spain, Wild Caught, Net Weight 4.1/10oz (115g), Empacado para:/Packaged for: Bacalafoods Corp., San Juan, PR 00936-8060
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-2455-2017·2017-07-12

    Meijer Cashews Recalled for Missing Coconut Allergen Labeling

    Meijer Distribution is recalling Meijer Cashews Toasted Coconut because the label lists a 'Contains' statement but omits coconut, a major allergen.

    Product
    MEIJER CASHEWS TOASTED COCONUT 8.25 OZ plastic pouch
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-2443-2017·2017-07-12

    Oxford Frozen Foods Recalls Ale House Onion Rings for Undeclared Milk

    Oxford Frozen Foods is recalling Ale House Beer Battered Onion Rings because the product may contain undeclared milk. This poses a risk to consumers with milk allergies.

    Product
    ALE HOUSE BEER BATTERED 3/8 ONION RINGS - NET WT. 4/2.5 lb (1.13 kg) 10 lb (4.54 kg) - 33221
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-2442-2017·2017-07-12

    Atlantic Gold Battered Onion Rings Recalled for Undeclared Milk

    Oxford Frozen Foods is recalling Atlantic Gold Battered Onion Rings because the product may contain undeclared milk.

    Product
    33034 33116 Thick Cut Regular Batter: ATLANTIC GOLD STEAK CUT BATTERED ONION RINGS NET WT 10 lb (4.54 kg) - 33166
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-2415-2017·2017-07-12

    GoMacro Recalls Thrive Caramel Coconut Bars for Listeria Risk

    GoMacro is recalling specific THRIVE Caramel Coconut bars because they may be contaminated with Listeria monocytogenes.

    Product
    go macro THRIVE Caramel Coconut bar, Net Wt 1.4 oz / 40 G, UPC 8 53555-00652 8
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·17185·2017-07-12

    TriggerTech Recalls Crossbow and Rifle Triggers Due to Injury Hazard

    TriggerTech is recalling about 2,000 carbide crossbow and rifle triggers because rollers can crack, causing the weapon to discharge without trigger activation.

    Product
    TriggerTech Carbide crossbow and rifle triggers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0938-2017·2017-07-12

    Xttrium Recalls Chlorhexidine Gluconate Oral Rinse Due to CGMP Deviations

    Xttrium Laboratories is voluntarily recalling 36,720 bottles of Chlorhexidine Gluconate 0.12% Oral Rinse due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    CHLORHEXIDINE GLUCONATE — CHLORHEXIDINE GLUCONATE (CHLORHEXIDINE GLUCONATE)
    Category
    Drug
    Distribution
    0 states
  • HighFDA (Food)·F-2451-2017·2017-07-12

    Slade Gorton Recalls Citrus Coconut Breaded Tilapia for Undeclared Milk

    Slade Gorton & Company is recalling Citrus Coconut Breaded Tilapia because it contains undeclared milk, a major food allergen.

    Product
    Gourmet Bay - Citrus Coconut Breaded Tilapia, 5-7 oz (Bulk 5 lbs) refrigerated Product Code: 7322401
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-2445-2017·2017-07-12

    Oxford Frozen Foods Recalls Beer Battered Onion Rings for Undeclared Milk

    Oxford Frozen Foods is recalling specific beer battered onion ring products because they may contain undeclared milk. The recall affects multiple states in the Northeast and Midwest.

    Product
    5/8" Thick Cut Beer Battered Onion Rings: ALE HOUSE BEER BATTERED STEAK CUT ONION RINGS NET WT. 4/2.5 lb 10 lb (4.45 kg) - 33223; OXFORD 5/8" Beer Battered Onion Rings 4-40oz (2.5 lb) 1.13kg Packages (Net Weight 10 lb (4.54kg) - 33145; Bellissimo Beer Battered Onion Rings Net Wei
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-2431-2017·2017-07-12

    Sea Watch Beer Battered Clam Strips Recalled for Undeclared Milk

    Sea Watch International is recalling Beer Battered Clam Strips because the bread coating may contain undeclared milk, a major allergen not listed on the label.

    Product
    Sea Watch Beer Battered Clam Strips Pack Size: 2/3 lb. bags/case
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-2435-2017·2017-07-12

    Don's Salads Recalls Chopped Herring Salad Due to Undeclared Milk

    Don's Salads is recalling Chopped Herring Salad because an ingredient used in its manufacture contains undeclared milk.

    Product
    Don's Salads; Chopped Herring Salad; Net Wt. 5 lbs., MFGD by Aldon Food Corp, Schwenksville, PA 19473; Sell By: 6/9, 6/11, 6/17, 6/24; UPC: 740247005023
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·F-2441-2017·2017-07-12

    Oxford Frozen Foods Recalls Battered Onion Rings for Undeclared Milk

    Oxford Frozen Foods is recalling specific brands of battered onion rings because they may contain undeclared milk.

    Product
    Thin Cut Regular Batter: BLUE ACRES BATTERED ONION RINGS, NET WT. 10 lb (4.54 kg) - 33049; ATLANTIC GOLD BATTERED ONION RINGS NET WT. 4/2.5 lb (1.13 kg) 10 lb (4.54 kg) - 33219; ATLANTIC GOLD Regular Battered Onion Rings 4-40oz (2.5 lb) 1.13kg Packages (Net Weight 10 lb (4.54kg)
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-2412-2017·2017-07-12

    Albertsons Recalls Carrot Cake Slices Due to Missing Walnut Allergen Labeling

    Albertsons is recalling 191,885 carrot cake slices sold in California because the packaging failed to list walnuts as an ingredient or allergen.

    Product
    Carrot Cake Slice: Net Wt. 0 LB 7 OZ (198 g). Cake is assembled, iced, sliced and packaged at store level. Sliced wrapped individually in clear plastic clamshell and sold in bakery department. UPC Code: 0222132-000000 Sold under Albertsons Companies retail banners of Von
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2685-2017·2017-07-12

    PerkinElmer Multiphor II Electrophoresis System Recalled for Electric Shock Risk

    PerkinElmer is recalling 241 Multiphor II Electrophoresis Systems due to a potential electric shock hazard if grommets are not installed.

    Product
    Multiphor II Electrophoresis System GE HealthCare Product Number: 18-1018-06 PerkinElmer Part Number: 2117-004 Product Usage: Multiphor II Electrophoresis System is a versatile modular electrophoresis system for horizontal electrophoresis, isoelectric focusing, 2-D elect
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2450-2017·2017-07-12

    Gourmet Bay Toasted Crumb Breaded Tilapia Recalled for Undeclared Milk

    Slade Gorton & Company is recalling refrigerated breaded tilapia due to undeclared milk. The product was distributed in seven states.

    Product
    Gourmet Bay - Toasted Crumb Breaded Tilapia, 5-7 oz. (Bulk 5 lbs container) refrigerated Product Code: 7396701
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-2434-2017·2017-07-12

    Don's Salads Recalls Magnum Shrimp Salad for Undeclared Milk

    Don's Salads is recalling Magnum Shrimp Salad because an ingredient used in its manufacture contains undeclared milk.

    Product
    Don's Salads; Magnum Shrimp Salad; Net Wt. 5 lbs., MFGD by Aldon Food Corp, Schwenksville, PA 19473; Sell By: 6/7, 6/12, 6/16, 6/26; UPC: 740247006013
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·F-2413-2017·2017-07-12

    GoMacro Recalls Specific MacroBars and Thrive Bars Due to Listeria Risk

    GoMacro is recalling specific MacroBars and Thrive Bars because they may be contaminated with Listeria monocytogenes.

    Product
    go macro MACROBAR, coconut + almond butter + chocolate chips, in the following sizes: 1. Net Wt 0.9 oz / 25 G minbar, UPC 8 53555-00671 9 and 2. net Wt 2.3 oz / 65 G, UPC 8 53555-00668 9
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2688-2017·2017-07-12

    Siemens Sensis Vibe Systems Recalled for Software Error in Report Generation

    Siemens is recalling 13 Sensis Vibe diagnostic computers in the US due to a software error that may combine patient data from different examinations into a single report.

    Product
    Sensis Vibe Systems with Software Version VD10B, Model Numbers 10765502, 10910620, 11007641, 6648161 --- Programmable diagnostic computer,
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-2656-2017·2017-07-12

    JAS Diagnostics Recalls Drew Scientific DREW 3-PAC Reagent Kits

    JAS Diagnostics Inc. is recalling 14,064 units of Drew Scientific DREW 3-PAC Reagent Kits because they may result in elevated platelet backgrounds during routine startup checks.

    Product
    Drew Scientific DREW 3-PAC Reagent Kit containing: 5L Diluent, 750 mL Enzymatic Cleaner, and 125 mL Lysing Reagent.
    Category
    Medical Device
    Distribution
    18 states
  • HighFDA (Food)·F-2449-2017·2017-07-12

    Amodio's Toasted Coconut Panko Recalled for Undeclared Milk

    Amodio's, Inc. is recalling Toasted Coconut Panko because the product may contain undeclared milk.

    Product
    Amodio's Toasted Coconut Panko sold in an 8 oz bags packaged in cases of 8.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-2418-2017·2017-07-12

    Schnucks Bakery Cinnamon Pudding Cake Recalled for Undeclared Walnuts

    Schnucks Markets is recalling Cinnamon Pudding Cakes because the labels fail to declare the presence of walnuts, a major food allergen.

    Product
    1) Schnucks Bakery, Cinnamon Pudding Cake Slice, NET WT 6.0 oz (170 g); 2) Schnucks Bakery, Half Cinnamon Pudding Cake, NET WT 1.06 lb (482 g);
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-2447-2017·2017-07-12

    Giant Eagle Recalls Toasted Crumb Tilapia Due to Undeclared Milk

    Giant Eagle is recalling Toasted Crumb Tilapia because it may contain undeclared milk. The product was distributed in Indiana, Maryland, Ohio, Pennsylvania, and West Virginia.

    Product
    Giant Eagle; Toasted Crumb Tilapia; various weights; Dist. By: Giant Eagle, Inc., Pittsburgh, PA PLU #69123. UPC: 691237 0054548
    Category
    Food
    Distribution
    5 states

Looking for a different month? Back to 2017.