Recalls for 08/18/2015

OxyTOTE Portable Oxygen Unit by Western/Scott Fetzer Company: Class I Recall - May Ignite and Burst
08/18/2015 Medical Recall

Reports of internal flash fire when the OxyTOTE is mishandled or dropped.

  • Category
    Health Care
Prolotherapy with Phenol by Hartley Medical: Recall - Non-sterility Concerns
08/18/2015 Medical Recall

Parenteral administration of non-sterile injection products may result in a site-specific or systemic infection, which in turn may cause hospitalization, significant morbidity, or a fatal outcome.

  • Company:
    Hartley Medical
2007 STARCRAFT ALLSTAR - EQUIPMENT:OTHER:LABELS
08/18/2015 Vehicle Recall

Starcraft Bus (Starcraft) is recalling certain model year 2002-2007 Allstar, Starquest, Starlite, and Ultrastar commercial buses manufactured January 1, 2002, to September 30, 2007. The affected vehicles, when loaded with passengers and fuel, may exceed the gross vehicle weight rating (GVWR). As such, these vehicles fail to comply with the requirements of 49 CFR Part 567, "Certification."

  • Company:
    STARCRAFT
  • Recall Number
    15V445000
2016 PETERBILT 365 - ELECTRICAL SYSTEM:ALTERNATOR/GENERATOR/REGULATOR
08/18/2015 Vehicle Recall

PACCAR Incorporated (PACCAR) is recalling certain model year 2012-2016 Peterbilt 365, 367, 384, 386, 388, 389, 567, 579, and 587 trucks manufactured January 13, 2011, to April 20, 2015. The affected trucks, equipped with extended-body Leece Neville alternators, have alternator charge cables that may chafe against a formed metal freon discharge line.

  • Company:
    Peterbilt
  • Recall Number
    15V456000
2016 KENWORTH T440 - SERVICE BRAKES, AIR
08/18/2015 Vehicle Recall

PACCAR Incorporated (PACCAR) is recalling certain model year 2016 Kenworth T440, T470, T660, T680, T800, T880, and W900 trucks manufactured February 16, 2015, to March 9, 2015. The affected vehicles are equipped with an SR-7 spring brake valve assembly that may have had the primary and secondary service brake applications installed in reverse. In the event of a failure in the primary or secondary circuit, the redundant circuit would not provide adequate service brake functionality. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) No. 121, "Air Brake Systems."

  • Company:
    PACCAR Incorporated
  • Recall Number
    15V457000
Merck Recalls Temodar and Temozolomide Bottles with Cracked Caps Due to Failure to Meet Child-Resistant Closure Requirement
08/18/2015 Product Recall

The bottle cap can be cracked which can cause the child-resistant closure to become ineffective to young children who can gain unintended access to the capsules, posing a risk of poisoning.

  • Company:
    Merck
  • Product:
    Bottles with cracked caps containing Temodar® (Temozolomide) and Temozolomide (generic) capsules
  • Problem
    Failure To Meet Child Resistant Closure Requirement
  • Recall Number
    15-219
Merck Recalls Temodar and Temozolomide Bottles with Cracked Caps Due to Failure to Meet Child-Resistant Closure Requirement
08/18/2015 Product Recall

The bottle cap can be cracked which can cause the child-resistant closure to become ineffective to young children who can gain unintended access to the capsules, posing a risk of poisoning.

  • Company:
    Merck
  • Product:
    Bottles with cracked caps containing Temodar® (Temozolomide) and Temozolomide (generic) capsules
  • Problem
    Failure To Meet Child Resistant Closure Requirement
  • Recall Number
    15-219
Tvilum Recalls Chairs Sold Exclusively at Copenhagen Imports Due to Fall Hazard (Recall Alert)
08/18/2015 Product Recall

The chair legs can break, posing a fall hazard for anyone sitting in the chair at the time.

  • Company:
    Copenhagen Imports
  • Product:
    Stars Mix n’Match Chairs
  • Problem
    Fall Hazard (Recall Alert)
  • Recall Number
    15-747
Tvilum Recalls Chairs Sold Exclusively at Copenhagen Imports Due to Fall Hazard (Recall Alert)
08/18/2015 Product Recall

The chair legs can break, posing a fall hazard for anyone sitting in the chair at the time.

  • Company:
    Copenhagen Imports
  • Product:
    Stars Mix n’Match Chairs
  • Problem
    Fall Hazard (Recall Alert)
  • Recall Number
    15-747
Rite Aid Recalls Outdoor Dining Sets Due to Fall Hazard
08/18/2015 Product Recall

The chair arms and legs can bend and cause the user to fall, posing a risk of injury.

  • Company:
    Rite Aid
  • Product:
    Outdoor Dining Sets
  • Problem
    Fire Hazard
  • Recall Number
    15-218
Rite Aid Recalls Outdoor Dining Sets Due to Fall Hazard
08/18/2015 Product Recall

The chair arms and legs can bend and cause the user to fall, posing a risk of injury.

  • Company:
    Rite Aid
  • Product:
    Outdoor Dining Sets
  • Problem
    Fire Hazard
  • Recall Number
    15-218
IKEA Recalls Children’s Nightlight Due to Electrical Shock Hazard
08/18/2015 Product Recall

The nightlight’s plastic covering can detach and expose electrical components, posing an electrical shock hazard.

  • Company:
    IKEA
  • Product:
    PATRULL Nightlight
  • Problem
    Impact And Burn Hazards
  • Recall Number
    15-217
IKEA Recalls Children’s Nightlight Due to Electrical Shock Hazard
08/18/2015 Product Recall

The nightlight’s plastic covering can detach and expose electrical components, posing an electrical shock hazard.

  • Company:
    IKEA
  • Product:
    PATRULL Nightlight
  • Problem
    Impact And Burn Hazards
  • Recall Number
    15-217
IKEA Recalls Children’s Nightlight Due to Electrical Shock Hazard
08/18/2015 Product Recall

The nightlight’s plastic covering can detach and expose electrical components, posing an electrical shock hazard.

  • Company:
    IKEA
  • Product:
    PATRULL Nightlight
  • Problem
    Impact And Burn Hazards
  • Recall Number
    15-217
Compounded Drugs Stored in Becton-Dickinson (BD) 3 ml and 5 ml Syringes: FDA Warning - Do Not Use
08/18/2015 Medical Recall

Preliminary information indicates that drugs stored in these syringes may lose potency over a period of time due to a possible interaction with the rubber stopper in the syringe.

  • Category
    Pharmacology
Hartley Medical Issues Voluntary Recall of Prolotherapy with Phenol Due to Non-sterility Concerns
08/18/2015 Food Recall

Hartley Medical is voluntarily recalling three lots of Prolotherapy with Phenol, Injectable to the hospital/user level due to non-sterility concerns.

  • Company:
    Hartley Medical
  • Problem
    Listeria Monocytogenes