Recalls for 02/25/2015

Colistimethate for Injection USP, 150 mg and Rifampin for Injection USP, 600 mg/vial by Heritage Pharmaceuticals: Recall - Lack of Sterility Assurance
02/25/2015 Medical Recall

Administration of non-sterile injection products may result in a site-specific or systemic infection, with the potential to cause hospitalization, permanent organ damage, or death.

  • Company:
    Heritage Pharmaceuticals Inc.
Magnetic Resonance Imaging (MRI) Systems with Magnet Rundown Unit by GE Healthcare: Class I Recall - Potential Disabling of the Magnet Rundown Unit
02/25/2015 Medical Recall

Risk of life-threatening injuries or death if a metal object is brought into the magnetic field.

  • Company:
    GE Healthcare
Heritage Pharmaceuticals Initiates a Nationwide Voluntary Recall of Colistimethate for Injection USP, 150 mg and Rifampin for Injection USP, 600 mg/vial Due to a Lack of Sterility Assurance
02/25/2015 Food Recall

Eatontown, NJ, Heritage Pharmaceuticals Inc. (Heritage) today announced the voluntary nationwide recall of ten (10) lots of Colistimethate for Injection, USP, 150 mg Single-Dose vial (NDC 23155-193-31) and three (3) lots of Rifampin for Injection, USP, 600 mg Single-Dose vial (NDC 23155-340-31) manufactured by Emcure Pharmaceuticals Ltd. and distributed by Heritage. Both products are sold in single vial mono-cartons in case packs of ten (10).

  • Company:
    Heritage Pharmaceuticals Inc.
  • Problem
    Undeclared Almond And Wheat
Fairway “Like No Other Market” Recalls Fairway Brand Raw Hazelnuts (Filberts) Because of Possible Health Risk
02/25/2015 Food Recall

Fairway “Like No Other Market” of New York, NY, is recalling Fairway brand Raw Hazelnuts (Filberts), because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain.

  • Company:
    Fairway “Like No Other Market”
  • Problem
    Salmonella
2014 FOREST RIVER FLAGSTAFF - EQUIPMENT
02/25/2015 Vehicle Recall

Forest River, Inc. (Forest River) is recalling certain model year 2014 Rockwood and Flagstaff recreational vehicles manufactured June 26, 2014, to October 9, 2014, and equipped with the Chill Chaser option. In the affected vehicles, excessive foam insulation and/or loose wiring may touch the Chill Chaser heating element.

  • Company:
    FOREST RIVER
  • Recall Number
    15V080000
2012 CHEVROLET CG33803 - EQUIPMENT ADAPTIVE
02/25/2015 Vehicle Recall

OBS, Inc. (OBS) is recalling certain model year 2012 Chevrolet CG33803 vehicles manufactured January 6, 2012, to January 9, 2013, 2007 Collins Midstar 20IS vehicles manufactured March 10, 2007, to August 27, 2007, Blue Bird A3FE2803a vehicles manufactured September 25, 2006, to March 23, 2007, and 2010 Blue Bird BBCV3011s vehicles manufactured May 10, 2009, to November 4, 2009, equipped with certain model S2005, S2010, S5005, S5010, S5505, and S5510 wheelchair lifts manufactured by Ricon Corporation. The platform side plate of the affected wheelchair lifts may crack.

  • Company:
    CHEVROLET
  • Recall Number
    15V068000
2012 CHEVROLET CG33803 - EQUIPMENT ADAPTIVE
02/25/2015 Vehicle Recall

OBS, Inc. (OBS) is recalling certain model year 2012 Chevrolet CG33803 vehicles manufactured January 6, 2012, to January 9, 2013, 2007 Collins Midstar 20IS vehicles manufactured March 10, 2007, to August 27, 2007, Blue Bird A3FE2803a vehicles manufactured September 25, 2006, to March 23, 2007, and 2010 Blue Bird BBCV3011s vehicles manufactured May 10, 2009, to November 4, 2009, equipped with certain model S2005, S2010, S5005, S5010, S5505, and S5510 wheelchair lifts manufactured by Ricon Corporation. The platform side plate of the affected wheelchair lifts may crack.

  • Company:
    BLUE BIRD
  • Recall Number
    15V068000
2012 CHEVROLET CG33803 - EQUIPMENT ADAPTIVE
02/25/2015 Vehicle Recall

OBS, Inc. (OBS) is recalling certain model year 2012 Chevrolet CG33803 vehicles manufactured January 6, 2012, to January 9, 2013, 2007 Collins Midstar 20IS vehicles manufactured March 10, 2007, to August 27, 2007, Blue Bird A3FE2803a vehicles manufactured September 25, 2006, to March 23, 2007, and 2010 Blue Bird BBCV3011s vehicles manufactured May 10, 2009, to November 4, 2009, equipped with certain model S2005, S2010, S5005, S5010, S5505, and S5510 wheelchair lifts manufactured by Ricon Corporation. The platform side plate of the affected wheelchair lifts may crack.

  • Company:
    COLLINS
  • Recall Number
    15V068000
2014 TOYOTA FJ CRUISER - STEERING
02/25/2015 Vehicle Recall

Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain model year 2014 FJ Cruiser vehicles manufactured August 7, 2013, to August 20, 2013. In the affected vehicles, the intermediate steering shaft which connects the steering wheel and the steering gear box may have an inadequate weld.

  • Company:
    Toyota Motor Engineering
  • Recall Number
    15V081000
2015 MERCEDES BENZ SPRINTER 2500 - STRUCTURE:BODY:DOOR
02/25/2015 Vehicle Recall

Mercedes-Benz USA, LLC - DBA Sprinter (Sprinter) is recalling certain model year 2015 Sprinter 2500 and 3500 vehicles manufactured July 1, 2014, to October 14, 2014. In the affected vehicles, the abutting wedge, a component attached to the door jam to make opening the door easier after a severe frontal impact, may have been installed incorrectly.

  • Company:
    MERCEDES BENZ
  • Recall Number
    15V082000
Cosco Recalls Convertible Hand Trucks Due to Injury Hazard
02/25/2015 Product Recall

The wheel hub can separate or break and eject pieces during inflation, posing a risk of injury to the consumer and bystanders.

  • Company:
    Cosco Home & Office Products
  • Product:
    Hand trucks
  • Problem
    Choking Hazard
  • Recall Number
    15-086
MAQUET Servo Humidifier 163 by Teleflex Medical: Class I Recall - Cracks in Connector Tubes May Lead to Leak Failures
02/25/2015 Medical Recall

Cracks may prevent device from delivering sufficient support to the patient. This may potentially cause serious injury or death.

  • Company:
    INMED