The Recall Desk

Archive

May 2015 recalls

653 recalls were announced in May 2015.

What the numbers show

Critical
52
Severe
145
High
352
Moderate
90
Low
14

Of the 653 recalls this month scored against our rubric, 8% are Critical, 22% are Severe.

401–500 of 653

  • HighFDA (Food)·F-2160-2015·2015-05-13

    Spiceco Recalls Seasoning Salt and Paprika for Undeclared Peanut

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

    Product
    Spice Eagle Brand Seasoning Salt BLN101200 Net Wt: 50 Lbs Packed by : Spiceco Avenel, New Jersey 07001
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1568-2015·2015-05-13

    Stryker Recalls Wound Drains for Potential Sterility Breach

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

    Product
    3/16 in. Round Drain with Trocar Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved trocar wound drain has a curved metal trocar attached to one end of the flexible wound drain tube. There is also a polymeric trocar guard that provides protection from th
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1562-2015·2015-05-13

    Stryker Recalls Trocar Wound Drains Due to Potential Sterility Breach

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

    Product
    3/16 in. Trocar with Single Drain Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved trocar wound drain has a curved metal trocar attached to one end of the flexible wound drain tube. There is also a polymeric trocar guard that provides protection from t
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1592-2015·2015-05-13

    ICU Medical Recalls MicroClave T-Connectors Due to Connection Separation Risk

    ICU Medical is recalling 13,800 MicroClave T-Connectors because potential connection separation issues could lead to leakage.

    Product
    108" (274 cm) Transfer Set w/Check Valve, MicroClave T-Connector, Anti-Siphon Valve, Clamp, Luer Lock, Non-DEHP Tubing, Item No. B33326
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1569-2015·2015-05-13

    Stryker Recalls Wound Drains Due to Potential Sterility Breach

    Stryker Instruments is voluntarily recalling specific wound drain devices because of a potential sterility breach in the packaging.

    Product
    1/4 in. Round Drain with Trocar Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved trocar wound drain has a curved metal trocar attached to one end of the flexible wound drain tube. There is also a polymeric trocar guard that provides protection from the
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2167-2015·2015-05-13

    Spiceco Recalls Seasoning Salt and Paprika for Undeclared Peanut

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

    Product
    Twin Tree Gardens Premium Spice Blends Seasoning Salt Net 5.5 oz (155 g) Distributed to Flavor Delite, Inc. Reinburg South Carolina PC4016
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1564-2015·2015-05-13

    Stryker Recalls Wound Drains for Potential Sterility Breach

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

    Product
    1/8 in. Trocar with Single Drain Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved trocar wound drain has a curved metal trocar attached to one end of the flexible wound drain tube. There is also a polymeric trocar guard that provides protection from th
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2158-2015·2015-05-13

    Spiceco Recalls Chicken Seasoning and Paprika Due to Undeclared Peanut

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

    Product
    Shoppers Value Chicken Seasoning 5 oz. - UPC 041130310676 Distributed By: Supervalu Inc., Eden Prairie, MN 55344 USA,
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2152-2015·2015-05-13

    Krystyna Bakery Polish Style Cheese Cake Recalled for Undeclared Ingredients

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

    Product
    Krystyna Bakery Polish Style Cheese Cake, Weight 18 oz., UPC 789438000096
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1578-2015·2015-05-13

    Philips EPIQ 5 Ultrasound Systems Recalled for Pediatric BSA Calculation Error

    Philips is recalling EPIQ 5 Ultrasound Systems with the Pediatric Cardiology option because a unit conversion error may cause incorrect Body Surface Area calculations.

    Product
    EPIQ 5 Ultrasound System with Pediatric Cardiology option, Model: EPIQ 5G, EPIC 5C, EPIQ 5W. Catalog Number: 795204 / 795205. Part Number: 989605408541 With 453561736761 (1.1) 453561750041 (1.1.1) 453561753651 (1.1.2) 453561772231 (1.2) 453561772611 (1.2.1) 453561786571 (1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2154-2015·2015-05-13

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

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

    Product
    Emeril's Cajun Seasoning Blend, 3.45 oz. (98g) Distributed by: B&G Foods, Inc., Parsippany, NJ 07054 USA, UPC 07468309979
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1565-2015·2015-05-13

    Stryker Recalls Wound Drains for Potential Sterility Breach

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

    Product
    1/8 in. Double Trocar with Wound Drain Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved trocar wound drain has a curved metal trocar attached to one end of the flexible wound drain tube. There is also a polymeric trocar guard that provides protection f
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2159-2015·2015-05-13

    Spiceco Recalls Fiesta Seasoned Salt for Undeclared Peanut

    Spiceco is recalling Fiesta Seasoned Salt because it may contain undeclared peanut protein. The recall includes additional products using the implicated paprika.

    Product
    Fiesta Seasoned Salt Net Wt 16 oz (1 LB) 454 g Distributed By Fiesta Mart Houston TX 77246-7481
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2143-2015·2015-05-13

    Trader Joe's A Dozen Sweet Bites Recalled for Undeclared Coconut

    Prolainat is recalling Trader Joe's A Dozen Sweet Bites cakes due to undeclared coconut, a major food allergen.

    Product
    TRADER JOES A Dozen Sweet Bites Chocolate and Coffee Opera Cake, Raspberry Macaroon Cake, Caramel & Chocolate Cake, 9.16 oz UPC 00967679 or SKU 096767.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1582-2015·2015-05-13

    Brainlab ExacTrac 6.x Software Recalled for Potential Positioning Errors

    Brainlab AG is recalling ExacTrac 6.x software due to potential patient positioning errors when using CBCT at non-zero couch angles.

    Product
    ExacTrac 6.x. is software used to place patients at an accurately defined point within the treatment beam of a medical accelerator for stereotactic radiosurgery or radiotherapy procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2164-2015·2015-05-13

    Spiceco Recalls Sweet Hungarian Paprika for Undeclared Peanut

    Spiceco, Inc. is recalling Pride of Szeged Sweet Hungarian Paprika and other products because they may contain undeclared peanut protein.

    Product
    Maison Royal labeled as ordered
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2156-2015·2015-05-13

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

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

    Product
    Sylvia's Rib Rub N More Seasoning, Net Wt. 5.5 oz. (155g), Distributed by: Sylvia Woods Food Company, P.O. Box 240, Harlem, NY 10027, UPC 608623000683
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1577-2015·2015-05-13

    Spacelabs Ultraview SL Command Modules Recalled for Random Resets

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

    Product
    Ultraview SL Command Modules, Model 91496, with the Masimo SpO2 PCBA, PN: 010-1636-02. The Spacelabs Multi-parameter Module is intended for use with the Patient Care Management System (PCMS) to acquire, monitor, and process various clinical parameters from an adult or neonate
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2175-2015·2015-05-13

    Cott Beverages Recalls Red Rain Energy Drink for Unlabeled Tree Nuts

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

    Product
    Red Rain Energy Drink Tropical Mango
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1573-2015·2015-05-13

    Stryker Recalls Ambulating Bulbs Due to Potential Sterility Breach

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

    Product
    Ambulating Bulb Ambulating Bulb: The Ambulating Bulb comprises four main components: the suction reservoir, the PVC tubing, the slide clamp and the female connector. The rigid polycarbonate female connector is used to connect the ambulating bulb to the CBCII evacuator tube in
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2181-2015·2015-05-13

    Cott Beverages Recalls Kroger Tropical Mango Shots for Unlabeled Walnut

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

    Product
    Kroger Shots Tropical Mango Flavor 2 pack
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1563-2015·2015-05-13

    Stryker Recalls Wound Drains Due to Potential Sterility Breach

    Stryker Instruments is voluntarily recalling specific wound drain products because the packaging may have a sterility breach.

    Product
    3/16 in. Double Trocar with Wound Drain Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved trocar wound drain has a curved metal trocar attached to one end of the flexible wound drain tube. There is also a polymeric trocar guard that provides protection
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1570-2015·2015-05-13

    Stryker Recalls Curved Trocar Wound Drains for Sterility Breach

    Stryker is voluntarily recalling 3/16 in. Curved Trocar with Wound Drain devices due to a potential sterility breach in the packaging.

    Product
    3/16 in. Curved Trocar with Wound Drain Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved trocar wound drain has a curved metal trocar attached to one end of the flexible wound drain tube. There is also a polymeric trocar guard that provides protection
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1572-2015·2015-05-13

    Stryker Recalls Curved Trocar Wound Drains for Sterility Breach

    Stryker Instruments is voluntarily recalling 1/4 in. Curved Trocar with Wound Drain devices due to a potential sterility breach in the packaging.

    Product
    1/4 in. Curved Trocar with Wound Drain Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved trocar wound drain has a curved metal trocar attached to one end of the flexible wound drain tube. There is also a polymeric trocar guard that provides protection f
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0974-2015·2015-05-13

    RemedyRepack Recalls Ketorolac Tromethamine Injection Due to Crystallization

    RemedyRepack Inc. is voluntarily recalling 25 vials of Ketorolac Tromethamine Injection 30 mg/mL due to crystallization. The product was distributed in Pennsylvania and Oklahoma.

    Product
    KETOROLAC TROM 30 MG/ML INJ, 1 mL glass vials repackaged individually inside an amber glass bottle, packaged by RemedyRepack, Indiana, PA, mfg by Hospira, Inc. Lake Forest, IL NDC 61786-0055-01
    Category
    Drug
    Distribution
    2 states
  • ModerateFDA (Food)·F-2170-2015·2015-05-13

    Mead Johnson Recalls Pregestimil 20 Calorie Bottles Due to Carton Labeling Error

    Mead Johnson Nutrition is recalling 235 cases of Pregestimil 20 Calorie Nursette bottles because some were packaged in 24 Calorie cartons. The bottles themselves are correctly labeled.

    Product
    Pregestimil ready to use 20 calorie, 2 oz bottle; 6 bottles per carton; 8 cartons per case
    Category
    Food
    Distribution
    28 states
  • ModerateFDA (Food)·F-2197-2015·2015-05-13

    EarthCoco Pure Coconut Water Recalled for Lack of 5-Log Reduction Process

    EarthCoco is recalling 320ml and 500ml bottles of Pure Coconut Water because they lack a required 5-log reduction process.

    Product
    Earth Coco Raw Coconut Water 100% Pure -320ml UPC 799632-585022 -500ml UPC 799632-585015 Distributed by: Earthcoco, Inc. 2651 Main Street Santa Monica CA 90405 www.earthcoco.com Product of Philippines **store frozen for maximum freshness**
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-0992-2015·2015-05-13

    Cody Laboratories Recalls C-Topical 4% Cocaine Hydrochloride Due to Labeling Error

    Cody Laboratories is recalling 19,139 bottles of C-Topical 4% cocaine hydrochloride because they were incorrectly labeled as 10 mL instead of 4 mL.

    Product
    C-Topical 4% CII (cocaine hydrochloride), topical solution, 4 ml bottle, (NDC 0527-1728-74), Rx Only, Manufactured for Lannett Company, Inc. Philadelphia, PA 19136 by Cody Laboratories, Inc. Cody, WY 82414
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0975-2015·2015-05-13

    Wockhardt Recalls Captopril Tablets for Thickness Specification Failures

    Wockhardt USA is recalling specific lots of Captopril Tablets 12.5 mg because they failed to meet thickness specifications.

    Product
    Captopril Tablets, USP 12.5 mg, Rx Only, a) 100 count bottles NDC 64679-902-01, b) 1000 count bottles NDC 64679-902-02, Manufactured by Wockhardt Limited, Mumbai, India, Distributed by: Wockhardt USA LLC., 20 Waterview Boulevard, Parsippany, NJ 07054 USA
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1581-2015·2015-05-13

    Siemens ACUSON SC2000 Ultrasound Systems Recalled for Image Capture Failures

    Siemens is recalling 186 ACUSON SC2000 ultrasound systems because they may fail to capture images or clips during routine scans.

    Product
    ACUSON SC2000 volume imaging ultrasound systems at software versions VA16C, VA16D and VA16E. Model 10433816. Product Usage: The SC2000 ultrasound imaging system is intended for the following applications: Cardiac, Neo-natal and Fetal Cardiac, Pediatric, Transespohageal, Adult
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1584-2015·2015-05-13

    Siemens ACUSON SC2000 Ultrasound Systems Recalled for Image Loss

    Siemens Medical Solutions USA is recalling 476 ACUSON SC2000 ultrasound systems because post-exercise images may be lost during Stress Echo procedures.

    Product
    ACUSON SC2000 ultrasound systems at software versions VA20A or VA20B. Model number 10433816. The SC2000 ultrasound imaging system is intended for the following applications: Cardiac, Neo-natal and Fetal Cardiac, Pediatric, Transespohageal, Adult Cephalic, Peripheral Vessel, A
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-0983-2015·2015-05-13

    Romark Recalls Alinia Powder for Oral Suspension Due to Stability Failure

    Romark Laboratories is recalling specific lots of Alinia (nitazoxanide) powder for oral suspension because the product failed to meet long-term stability specifications for viscosity.

    Product
    Alinia (nitazoxanide), powder for oral suspension, 100mg/5mL, 60 mL/bottle. Rx only, Manufactured for Lupin Pharmaceuticals Inc, Baltimore, Maryland 21202 for Romark Laboratories 3000 Bayport Dr. Suite 200, Tampa, FL 33607
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1566-2015·2015-05-13

    Stryker Recalls Wound Drains for Potential Sterility Breach

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

    Product
    1/4 in. Trocar with Single Drain Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved trocar wound drain has a curved metal trocar attached to one end of the flexible wound drain tube. There is also a polymeric trocar guard that provides protection from th
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1571-2015·2015-05-13

    Stryker Recalls Curved Trocar Wound Drains for Potential Sterility Breach

    Stryker Instruments is voluntarily recalling 1/8 in. Curved Trocar with Wound Drain devices due to a potential sterility breach in the packaging.

    Product
    1/8 in. Curved Trocar with Wound Drain Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved trocar wound drain has a curved metal trocar attached to one end of the flexible wound drain tube. There is also a polymeric trocar guard that provides protection f
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1575-2015·2015-05-13

    Zimmer NexGen Augment Recalled for Missing Locking Screw

    Zimmer, Inc. is recalling 20 units of NexGen Augment knee implants because they were packaged without the required locking screw, which may delay surgery.

    Product
    NexGen Augment; 5mm Distal Femoral Augment;Part number 00-5990-036-10. Intended to be used in total knee arthroplasty when there is insufficient bone in the distal femur.
    Category
    Medical Device
    Distribution
    4 states
  • LowFDA (Devices)·Z-1587-2015·2015-05-13

    Stryker Universal Battery Charger Recalled for Software Data Transmission Issue

    Stryker is recalling 223 Universal Battery Chargers because they are not transmitting usage data to the Stryker Cloud as designed. A software correction is being initiated.

    Product
    Universal Charger Product Usage: The Stryker Universal Battery Charger is designed to be used in conjunction with and provide power to non-sterile and sterile batteries. The Stryker Universal Battery Charger is a four station, modular battery charger intended to charge S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1585-2015·2015-05-13

    Fujifilm Aspire HD Mammography System Recalled for User Manual Error

    Fujifilm is recalling one Aspire HD mammography system in Hawaii because the user manual lacks descriptions for handling certain recoverable errors.

    Product
    Aspire HD, Full Field Digital, System, x-Ray, Mammographic; Model: FOR MS-1000. A mammography system used for screening and diagnosis of breast cancer.
    Category
    Medical Device
    Distribution
    1 state
  • SevereNHTSA·15V279000·2015-05-12

    Ford Recalls 2015 F-150 Trucks for Steering Shaft Rivet Defect

    Ford is recalling 2015 F-150 trucks because an improperly riveted steering shaft could separate, causing loss of steering control and increasing crash risk.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V278000·2015-05-12

    GM Recalls 2015 Chevrolet Colorado and GMC Canyon for Brake Caliper Leaks

    General Motors is recalling 2015 Chevrolet Colorado and GMC Canyon trucks because front brake calipers may leak fluid, increasing stopping distance and crash risk.

    Product
    GMC — GMC, CHEVROLET CANYON, COLORADO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·15133·2015-05-12

    IKEA Recalls Pressure-Mounted Safety Gates Due to Fall Hazard

    IKEA is recalling PATRULL KLÄMMA and PATRULL SMIDIG safety gates because they may fail to hold in place, posing a fall hazard. Consumers should stop using the gates and return them for a refund.

    Product
    PATRULL KLÄMMA and PATRULL SMIDIG Safety Gates
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E038000·2015-05-12

    Fleetline Recalls Fender Brackets Due to Insufficient Welds

    Fleetline is recalling specific Nu-Line and Fleetline fender brackets and kits due to insufficient welds that may cause fender separation.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V277000·2015-05-12

    Blue Bird Recalls 2016 School Buses for Seat Flammability Defect

    Blue Bird is recalling 2016 Vision and All American school buses because seat foam may not meet federal flammability standards, increasing fire risk.

    Product
    BLUE BIRD — BLUE BIRD VISION, ALL AMERICAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V276000·2015-05-12

    MCI D4000 and D4500 Motorcoaches Recalled for Engine Fire Risk

    Motor Coach Industries is recalling 2011-2012 D4000 and 2014-2015 D4500 motorcoaches because a vent tube defect may allow engine oil to contact hot surfaces, increasing fire risk.

    Product
    MCI — MCI D4500, D4000
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15731·2015-05-12

    La-Z-Boy Recalls PowerReclineXRw Furniture Due to Fall Hazard

    La-Z-Boy is recalling about 2,600 PowerReclineXRw recliners and loveseats because they can tip forward when reclined, posing a fall hazard.

    Product
    PowerReclineXRw
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V272000·2015-05-11

    Kenworth Recalls 2016 Trucks Due to Potential Rear Wheel Separation

    PACCAR is recalling specific 2016 Kenworth trucks because rear wheels may be loose due to a missed torque verification step, increasing crash risk.

    Product
    KENWORTH — KENWORTH T660, T680, T880, T800
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V274000·2015-05-11

    Volvo Recalls 2012-2016 VNM Trucks Due to Engine Fire Risk

    Volvo is recalling 2012-2016 VNM trucks because a vent tube may detach, allowing engine oil to contact hot surfaces and increase fire risk.

    Product
    VOLVO — VOLVO VNM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V275000·2015-05-11

    Mack Trucks Recall 2011-2016 Models for Engine Fire Risk

    Mack is recalling 2,124 trucks due to a vent tube defect that could allow engine oil to contact hot surfaces, increasing fire risk.

    Product
    MACK — MACK LR6, LEU, MRU
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V273000·2015-05-11

    Forest River Recalls Trailers Due to Failing Entry Step Rivets

    Forest River is recalling specific 2013-2015 RV trailers because a rivet on the quad entry steps may shear, causing the steps to fail and increasing the risk of injury.

    Product
    FOREST RIVER — FOREST RIVER CEDAR CREEK, DYNAMAX, SIERRA, CARDINAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V270000·2015-05-08

    PACCAR Recalls Kenworth and Peterbilt Trucks Due to Fire Risk

    PACCAR is recalling specific Kenworth and Peterbilt trucks because alternator cables may chafe against a metal line, creating a fire risk.

    Product
    PETERBILT — PETERBILT, KENWORTH 567, 579, 587, T660
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V267000·2015-05-08

    GM Recalls 2015 Chevrolet Colorado and GMC Canyon Trucks for Seat Defect

    General Motors is recalling 2015 Chevrolet Colorado and GMC Canyon trucks because seat frame hooks may not be properly attached, increasing injury risk in a crash.

    Product
    GMC — GMC, CHEVROLET CANYON, COLORADO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V268000·2015-05-08

    Ducati Recalls 2014 Panigale and Superleggera Motorcycles for Rear Shock Defect

    Ducati is recalling 549 model year 2014 1199 Panigale and Superleggera motorcycles because a rear shock absorber nut may loosen, potentially causing a loss of vehicle control.

    Product
    DUCATI — DUCATI 1199 PANIGALE, 1199 SUPERLEGGERA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V271000·2015-05-08

    Kenworth Trucks Recalled for Wiper Motor Water Leak and Fire Risk

    PACCAR is recalling 2011-2016 Kenworth trucks because water may leak into the wiper motor, causing wiper failure and potential electrical fires.

    Product
    KENWORTH — KENWORTH 963, T470, T440, T370
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V269000·2015-05-08

    GM Recalls 2011-2012 Chevrolet Malibu for Seat Belt Cable Defect

    General Motors is recalling 2011-2012 Chevrolet Malibus because flexible steel seat belt cables may break, increasing injury risk in a crash.

    Product
    CHEVROLET — CHEVROLET MALIBU
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·077-2015·2015-05-08

    Walker's Foods Recalls Pork Products Due to Undeclared Soy Allergen

    Walker's Foods is recalling approximately 46,612 pounds of pork with sauce products because they contain soy, an undeclared allergen.

    Product
    Walker Foods, Inc. — Walker's Foods Recalls Pork Products Due To Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    2 states
  • HighCPSC·15131·2015-05-08

    Baby's Dream Recalls Vintage Gray Cribs and Furniture for Lead Paint

    Baby's Dream is recalling approximately 4,600 cribs, furniture pieces, and accessories with vintage gray paint because the paint exceeds federal lead limits.

    Product
    Cribs, furniture and accessories with vintage gray paint finish
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V265000·2015-05-07

    Thor Motor Coach Recalls 2016 Hurricane and Windsport Motorhomes for Seat Defect

    Thor Motor Coach is recalling 2016 Hurricane and Windsport motorhomes because the co-pilot seat mounting area may not be properly reinforced, increasing injury risk in a crash.

    Product
    THOR MOTOR — THOR MOTOR, THOR MOTOR COACH HURRICANE, WINDSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·075-2015·2015-05-07

    Khubba Al Nahrain Recalls Beef Products Due to Undeclared Allergens

    Khubba Al Nahrain Inc. is recalling approximately 665 pounds of beef products because they contain undeclared wheat, soy, and milk.

    Product
    Archie's Foods, Inc. — Khubba Al Nahrain Inc. Recalls Beef Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    2 states
  • SevereNHTSA·15E035000·2015-05-07

    Curt Manufacturing Recalls U-Haul Power Tow Towing Starter Kits

    Curt Manufacturing is recalling U-Haul Power Tow Towing Starter Kits because the ball mount tongue may break, potentially causing the trailer to disengage.

    Product
    TRAILER HITCHES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E037000·2015-05-07

    Curt Manufacturing Recalls U-Haul Power Tow Towing Starter Kits

    Curt Manufacturing is recalling U-Haul Power Tow Towing Starter Kits because the ball mount tongue may break, potentially causing the trailer to disengage.

    Product
    TRAILER HITCHES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·15129·2015-05-07

    Franklin Recalls Power Reclining Furniture Due to Fire Hazard

    Franklin Corporation is recalling about 81,000 power reclining furniture units because the operating switch can overheat and cause a fire.

    Product
    Power reclining furniture
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·076-2015·2015-05-07

    SP Wholesale Meats Recalls Sausage Products Due to Undeclared Wheat Allergen

    SP Wholesale Meats is recalling approximately 1,729 pounds of raw pork and chicken sausage products because they contain undeclared wheat, a known allergen.

    Product
    SP Provisions — SP Wholesale Meats Recalls Sausage Products Due To Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    2 states
  • HighNHTSA·15V266000·2015-05-07

    Jayco Recalls 2013-2015 Trailers Due to Failing Entry Step Rivets

    Jayco is recalling 2,747 model year 2013-2015 Seismic and Eagle Premier trailers because entry step rivets may shear, causing steps to fail and occupants to fall.

    Product
    JAYCO — JAYCO, JAYCO FIFTH WHEEL EAGLE PREMIER, SEISMIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15130·2015-05-07

    Snow Peak Recalls Japanese Axe M Due to Handle Cracking Hazard

    Snow Peak is recalling about 220 Japanese Axe M units because the handle can crack, allowing the axe head to come loose and posing a laceration or impact hazard.

    Product
    Japanese Axe M
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2043-2015·2015-05-06

    Giant Eagle Recalls Iced Cut Out Cookies Due to Undeclared Milk

    Giant Eagle is recalling iced cut out cookies sold in its bakeries because they contain an undeclared milk allergen.

    Product
    All varieties and packaging configurations of iced cut out cookies, labeled as Decorated Cut Out Cookie and Cut Out Cookies, 1oz and 2oz sold individually behind the bakery department service counter, and also pre-packaged in 2 counts (5oz), 10 counts (15oz), inside clear plastic
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-2139-2015·2015-05-06

    JCB Flavors Recalls Seasonings Containing Peanut Allergen

    JCB Flavors is recalling specific seasonings that used ground cumin containing trace peanut allergens. The recall affects products distributed to several states.

    Product
    JCB FLAVORS, LLC, Product Code 10044001, 10044002, 10044009, 1004425, Chili Powder #100440, "1 x 5lb jug, 4 x 5 lb jugs, 4x5lb bags, 25 lb bulk, 10 lb bulk, 12 x 8 oz". UPC 014641000183, 014641000176.
    Category
    Food
    Distribution
    7 states
  • CriticalFDA (Food)·F-2082-2015·2015-05-06

    Sabra Classic Hummus Recalled Due to Listeria Monocytogenes Contamination

    Sabra Dipping Company is recalling 10 oz Classic Hummus after a Michigan sample tested positive for Listeria monocytogenes.

    Product
    Sabra Classic Hummus 10 oz UPC 040822011143 / 300067, Sabra Dipping Co. LLC, White Plains, NY
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2120-2015·2015-05-06

    JCB Flavors Recalls Ground Cumin Seasonings Due to Peanut Allergen

    JCB Flavors is recalling various seasonings containing ground cumin because the ingredient tested positive for trace peanut allergens.

    Product
    JCB FLAVORS, LLC, Product Code 4006500812 / 40650/406500812/771756/ 40650, Cumin Ground #400650/40650/44650, 12x 8oz jar, 12x 3.4 oz jar, 12 x 16 oz jar, 1 x 16 oz jar, ,4 x 5 lb jug, bulk ( 25 lb, 10 lb, 2 lb) , UPC: 66049248116, 66049248106, 66049248125, 014641001128, 01464
    Category
    Food
    Distribution
    7 states
  • CriticalFDA (Food)·F-2045-2015·2015-05-06

    Giant Eagle Recalls Cut Out Cookies Due to Undeclared Milk Allergen

    Giant Eagle is recalling Cut Out Cookies sold in its bakeries because they contain an undeclared milk allergen, which was identified after a consumer reported an allergic reaction.

    Product
    All varieties and packaging configurations of cut out cookies labeled as Cut Out Cookies 12-Pack, 24 oz., inside clear plastic containers,"processed on shared equipment" statement on label, sold exclusively at the Market District bakery department service counter .
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-2044-2015·2015-05-06

    Giant Eagle Recalls Cut Out Cookies Due to Undeclared Milk Allergen

    Giant Eagle is recalling cut out cookies sold in its bakeries because they contain an undeclared milk allergen. The recall follows a consumer complaint of an allergic reaction.

    Product
    All varieties and packaging configurations of tinted sugar decorated cut out cookies labeled as Cut Out Cookies and OTC Seasonal Cut Out Cookie, 1oz and 2oz sold individually behind the bakery department service counter and also pre-packaged in 2 counts (5oz), 10 counts (15oz), i
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-2141-2015·2015-05-06

    Red River Foods Recalls Macadamia Nuts Due to Salmonella Risk

    Red River Foods is voluntarily recalling 13,750 lbs of South Africa Macadamia Nuts after a repacker in Texas tested positive for Salmonella.

    Product
    Style 2 South Africa Macadamia Nuts,
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-2115-2015·2015-05-06

    JCB Flavors Recalls Chili Powder Due to Peanut Allergen Contamination

    JCB Flavors is recalling specific lots of chili powder and seasonings because the ground cumin ingredient tested positive for trace peanut allergens.

    Product
    JCB FLAVORS, LLC, Product Code 8102920812, 8102923212, 8102921606, Chili Powder #810292 , 12 x 8oz jar, UPC: 66049244520, 66049244506.
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·F-2083-2015·2015-05-06

    Sabra Classic Hummus Recalled Due to Listeria Monocytogenes Detection

    Sabra Dipping Company is recalling 30 oz Classic Hummus after a Michigan sample tested positive for Listeria monocytogenes.

    Product
    Sabra Classic Hummus 30 oz UPC 040822014687 / 300074 , Sabra Dipping Co. LLC, White Plains, NY
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2084-2015·2015-05-06

    Sabra Classic Hummus Recalled Due to Listeria Monocytogenes Contamination

    Sabra Dipping Company is recalling 32-ounce containers of Classic Hummus without Garnish after a sample tested positive for Listeria monocytogenes.

    Product
    Sabra Classic Hummus without Garnish 32oz UPC 040822342049 / 301216 Sabra Dipping Co. LLC, White Plains, NY
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2036-2015·2015-05-06

    Giant Eagle Bolillo Wheat Rolls Recalled for Undeclared Egg

    Giant Eagle is recalling Bolillo Wheat Rolls because they contain undeclared egg. Consumers with this product should not eat it.

    Product
    BOLILLO WHEAT ROLL; PLU: 97754; NET WT: 14oz.; Contains: Wheat, Soy
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-2033-2015·2015-05-06

    Giant Eagle Cheese Danish Recalled for Undeclared Egg Allergen

    Giant Eagle is recalling Cheese Danish products containing undeclared egg. Consumers with egg allergies should not consume these items.

    Product
    CHEESE DANISH 2 COUNT; PLU: 59779; NET WT 6.0 oz.; CONTAINS: WHEAT, SOY, MILK; In clear plastic clamshell
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-1536-2015·2015-05-06

    Baxter Patient Control Modules Recalled for Potential Malfunction

    Baxter Healthcare is recalling 7,596 Patient Control Modules due to a potential malfunction that could cause medication to flow when it should not.

    Product
    The Patient Control Module (PCM) is used in conjunction with a Baxter infusor as a single use device for the control of intermittent bolus doses of medication based on patient demand.
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Food)·F-2041-2015·2015-05-06

    Vital Labs Halo-V Recalled for Containing Anabolic Steroid

    A2Z Industries is recalling Vital Labs Halo-V dietary supplements because the product contains an anabolic steroid.

    Product
    Vital Labs Halo-V, 80 Capsules, Dietary Supplement, Supplement Facts: Serving Size: 1 Capsule, Servings per Container: 80, Amount Per Serving, 4-Chloro-17 a-Methyl-Android-1,4-Dieme-3-17b-Diol 25mg Other ingredients: Gelatin, Magnesium Stearate, Rice Flour Vital Labs,
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·F-2086-2015·2015-05-06

    Sabra Hummus Recalled Due to Listeria Monocytogenes Contamination

    Sabra Dipping Company is recalling specific tubs of Roasted Garlic and Classic Hummus after a Michigan sample tested positive for Listeria monocytogenes.

    Product
    Sabra Roasted Garlic Hummus, Classic Hummus packed in 2/23.5 oz plastic tub/package. UPC 040822342209, Sabra Dipping Co. LLC, White Plains, NY
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0971-2015·2015-05-06

    Teva Recalls Fluoxetine Capsules Due to Residual Solvent Impurity

    Teva Pharmaceuticals USA is recalling specific lots of Fluoxetine Capsules USP, 20 mg, due to an elevated level of a residual solvent impurity in the active pharmaceutical ingredient.

    Product
    FLUOXETINE — FLUOXETINE (FLUOXETINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2062-2015·2015-05-06

    Con Yeager Spice Company Recalls Ground Cumin for Undeclared Peanuts

    Con Yeager Spice Company is recalling specific lots of ground cumin and cumin seeds because they may contain undeclared peanuts.

    Product
    GROUND CUMIN and GROUND CUMIN SEEDS Con Yeager Spice Company, Zelienople, PA 16063 Net Weight: 10 lbs; UPC: 33385; Lot #: 6820; Net Weight: 5 lbs; UPC: 33385; Lot #: 6820; Net Weight: 1.5 oz; UPC: 30491; Lot #: .217751; .218400; .218560; Net Weight: 7 oz; UPC: 31049; Lot #
    Category
    Food
    Distribution
    20 states
  • SevereFDA (Food)·F-2079-2015·2015-05-06

    Giant Eagle Recalls Fried Fish and Meringue Pies for Undeclared Allergens

    Giant Eagle is recalling store-produced fried fish and meringue pies due to undeclared allergens. Consumers should stop eating these products.

    Product
    8" Coconut Meringue Pie Sell By: 04/02/15 PLU: 9963 Net Wt: 25oz. Contains: Wheat, Soy, Coconut, Egg
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-2085-2015·2015-05-06

    Sabra Classic Hummus Recalled Due to Listeria Monocytogenes Contamination

    Sabra Dipping Company is recalling Sabra Classic Hummus after a sample tested positive for Listeria monocytogenes. The product was distributed nationwide.

    Product
    Sabra Classic Hummus, 17oz Six Pack UPC 040822017497 / 301290 Sabra Dipping Co. LLC, White Plains, NY
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2035-2015·2015-05-06

    Giant Eagle Bolillo Rolls Recalled for Undeclared Egg

    Giant Eagle is recalling Bolillo Rolls 6 Count because they contain undeclared egg. The product was sold in Maryland, Ohio, Pennsylvania, and West Virginia.

    Product
    BOLILLO ROLLS 6 COUNT; PLU: 27754; NET WT: 11OZ.; CONTAINS: WHEAT, SOY
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-2080-2015·2015-05-06

    Supervalu Recalls Chocolate Covered Raisins for Undeclared Peanuts

    Supervalu is recalling Essential Everyday Chocolate Covered Raisins because the product may contain undeclared peanuts.

    Product
    Essential Everyday Chocolate Covered Raisins, Net Wt. 32 oz. in Clear plastic tub with black lid. UPC Code 41303-05311
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Drugs)·D-0973-2015·2015-05-06

    Hospira Recalls Ketorolac Tromethamine Injections Due to Crystallization

    Hospira is voluntarily recalling specific lots of Ketorolac Tromethamine Injections because of crystallization. The affected products were distributed nationwide, in Puerto Rico, and in Guam.

    Product
    Ketorolac Tromethamine Inj. USP, 60 mg (30 mg/mL), 2 mL Fill, Single-dose vial, Rx Only, Hospira Inc., Lake Forest, IL --- NDC 00409-3796-01 --- Also labeled under NOVAPLUS label NDC 00409-3796-49
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2034-2015·2015-05-06

    Giant Eagle Danish With Fruit Recalled for Undeclared Egg

    Giant Eagle is recalling Danish With Fruit products due to undeclared egg. Consumers with this product should not eat it.

    Product
    DANISH WITH FRUIT 2 COUNT; PLU: 69779; NET WT 6.0 oz.; CONTAINS: WHEAT, SOY, MILK; In clear plastic clamshell
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-1519-2015·2015-05-06

    Lumenis Light Sheer Desire Diode Laser System Recalled for Software Error

    Lumenis is recalling 117 Light Sheer Desire Diode Laser Systems because software parameters exceed manual settings, potentially causing burns.

    Product
    Light Sheer Desire Diode Laser System with XC Handpiece Accessory options.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2090-2015·2015-05-06

    Navajo Pride Flour Recalled for Salmonella Contamination

    Navajo Agricultural Products Industry is recalling Navajo Pride Bleached All Purpose Flour due to Salmonella contamination.

    Product
    Navajo Pride Bleached All Purpose Flour in 50 lb, 25 lb, and 5 lb Cloth Bags by Navajo Agricultural Products Industry.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2114-2015·2015-05-06

    JCB Flavors Recalls Chili Powder Dark Due to Peanut Allergen

    JCB Flavors is recalling Chili Powder Dark because it contains trace peanut allergens from a cumin ingredient.

    Product
    JCB FLAVORS, LLC, Product Code 8103060812, 8103063212, 8103061606, Chili Powder Dark #810306 ,12x4.25oz jar, 12 x 20 oz jar, 12 x 8oz jar, 6 x 6 lb jug,UPC 66049243520_, 66049243506_, 66049243525_
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-2077-2015·2015-05-06

    Giant Eagle Recalls Fried Fish and Pies for Undeclared Allergens

    Giant Eagle is recalling store-produced fried fish and meringue pies due to undeclared allergens. Consumers should not eat these products.

    Product
    Heat & Serve Fried Fish Sell By: (up to and including) 4/02/15 PLU: 37156 Contains Fish (Pangasus), Soy, Wheat Giant Eagle Distributed by: Giant Eagle, inc., Pittsburgh, PA 15238
    Category
    Food
    Distribution
    0 states

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