Recalls for 02/09/2014

2014 KENWORTH C500 - SEAT BELTS
02/09/2014 Vehicle Recall

PACCAR Incorporated (PACCAR) is recalling certain model year 2014 Kenworth T660, T680, T700,T800, T880, W900, T440, T470, T370, T270, T170, C500, and C550 chassis manufactured between August 7, 2013, and October 31, 2013, and Peterbilt 320, 325, 330, 337, 348, 365, 367, 382, 384, 386, 388, 389, and 587 chassis manufactured between August 7, 2013, and November 3, 2013, and equipped with IMMI-brand L9 seat belt buckles. When the button is pressed to release the seat belt, the latch plate can become partially engaged with the buckle, making the seat belt difficult to unlatch. Thus, these vehicles fail to conform to the requirements of Federal Motor Vehicle Safety Standard (FMVSS) No. 209, "Seat Belt Assemblies."

  • Company:
    PACCAR Incorporated
  • Recall Number
    14V013000
2014 KENWORTH C500 - SEAT BELTS
02/09/2014 Vehicle Recall

PACCAR Incorporated (PACCAR) is recalling certain model year 2014 Kenworth T660, T680, T700,T800, T880, W900, T440, T470, T370, T270, T170, C500, and C550 chassis manufactured between August 7, 2013, and October 31, 2013, and Peterbilt 320, 325, 330, 337, 348, 365, 367, 382, 384, 386, 388, 389, and 587 chassis manufactured between August 7, 2013, and November 3, 2013, and equipped with IMMI-brand L9 seat belt buckles. When the button is pressed to release the seat belt, the latch plate can become partially engaged with the buckle, making the seat belt difficult to unlatch. Thus, these vehicles fail to conform to the requirements of Federal Motor Vehicle Safety Standard (FMVSS) No. 209, "Seat Belt Assemblies."

  • Company:
    PACCAR Incorporated
  • Recall Number
    14V013000
Flat Creek Farm & Dairy Recalls Cheese Because of Possible Health Risk Update to Correcy Lot Number Information
01/22/2014 Food Recall

On December 23, 2013, Flat Creek Farm & Dairy of Swainsboro, GA announced a recall of its Heavenly Blue Cheese and Aztec Cheddar cheese. The purpose of this updated press release is to provide the correct lot number for the Aztec Cheddar cheese.

  • Company:
    Aztec Cheddar
  • Problem
    Salmonella
Trufill n-BCA Liquid Embolic System by Codman Neuro: Recall - Incorrect Instructions For Use
01/22/2014 Medical Recall

Incorrectly mixed product can result in the liquid mixture solidifying too slowly and could result in significant impact to the patient, including neurological deficits, pulmonary emboli and possibly death.

  • Company:
    Codman Neuro
Lochiel Enterprises Limited Recalls St Mary’s River Smokehouses Oven Smoked Salmon Stix, Chili Mango Flavor Because of Possible Health Risk
01/22/2014 Food Recall

Lochiel Enterprises Limited of Sherbrooke, NS is voluntarily recalling 56 lbs of ST MARY’S RIVER SMOKEHOUSES OVEN SMOKED ATLANTIC SALMON STIX, CHILI MANGO FLAVOR, because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and still births among pregnant women.

  • Company:
    Lochiel Enterprises Limited
  • Problem
    Listeria Monocytogenes
FDA Classifies Worldwide Voluntary Correction Notice on TRUFILL® n-BCA Liquid Embolic System as Class I Recall
01/22/2014 Food Recall

Codman Neuro announced today that the U.S. Food and Drug Administration (FDA) has classified the recently initiated medical device correction notice related to the TRUFILL® n-BCA Liquid Embolic System as a Class I recall.

  • Company:
    Codman Neuro
  • Problem
    Incorrect Statement In The Package Instructions For Use
Dream Body Slimming Capsule: Public Notification - Undeclared Drug Ingredient
01/22/2014 Medical Recall

Sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias, or stroke.

  • Category
    Myocardial Infarction
Magic Slim: Public Notification - Undeclared Drug Ingredient
01/22/2014 Medical Recall

Sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias, or stroke.

  • Category
    Hypertension
Nationwide Industries Recalls Trident Pool Gate Latches Due To Failure to Secure Hazardous Areas
01/22/2014 Product Recall

The magnet on the gate latches can loosen and fail to secure the gate properly.

  • Company:
    Nationwide Industries, Inc., of Tampa, Fla.
  • Product:
    Nationwide Industries Trident Pool Gate Latches
  • Problem
    Amputation And Laceration Hazards
  • Recall Number
    14-085
Nationwide Industries Recalls Trident Pool Gate Latches Due To Failure to Secure Hazardous Areas
01/22/2014 Product Recall

The magnet on the gate latches can loosen and fail to secure the gate properly.

  • Company:
    Nationwide Industries, Inc., of Tampa, Fla.
  • Product:
    Nationwide Industries Trident Pool Gate Latches
  • Problem
    Amputation And Laceration Hazards
  • Recall Number
    14-085
Playtex Recalls Pacifier Holder Clips Due to Choking Hazard
01/22/2014 Product Recall

The pacifier holder clips can crack and a small part can break off. The binky clips were sold from July 2010 through October 2013.

  • Company:
    Playtex
  • Product:
    Playtex pacifier holder clips
  • Problem
    Choking Hazard
  • Recall Number
    14-084
Baby Rattles Recalled by Midwest-CBK Due to Choking Hazard
01/22/2014 Product Recall

The head on the bear, monkey and lion rattles can detach.

  • Company:
    Midwest-CBK LLC, of Cannon Falls, Minn.
  • Product:
    Baby rattles
  • Problem
    Choking Hazard
  • Recall Number
    14-083