Recalls for 04/23/2014

2014 RANGE ROVER EVOQUE - SUSPENSION:REAR
04/23/2014 Vehicle Recall

Jaguar Land Rover North America, LLC (Land Rover) is recalling certain model year 2014 Range Rover Evoque vehicles manufactured November 27, 2013 and December 4, 2013. The bolts connecting the right hand rear suspension link arm may have been damaged during vehicle production.

  • Company:
    Jaguar Land Rover North America
  • Recall Number
    14V155000
2014 JAGUAR XF - SUSPENSION:REAR
04/23/2014 Vehicle Recall

Jaguar Land Rover North America, LLC (Jaguar) is recalling certain model year 2013-2014 XJ, XF and XK vehicles. In the affected vehicles, the toe links, components used to control the alignment of the rear wheels, can separate from the rear sub-frame.

  • Company:
    Jaguar Land Rover North America
  • Recall Number
    14V157000
2014 CHEVROLET CRUZE - POWER TRAIN:AXLE ASSEMBLY:AXLE SHAFT
04/01/2014 Vehicle Recall

General Motors LLC (GM) is recalling certain model year 2013 and 2014 Chevrolet Cruze vehicles equipped with a 1.4L turbo engine, and manufactured between November 28, 2012, and March 7, 2014. On the affected vehicles, the right front half shaft may fracture and separate.

  • Company:
    General Motors LLC
  • Recall Number
    14V151000
Nova Products, Inc. Issues Voluntary Nationwide Recall of Dietary Supplements with Undeclared Active Pharmaceutical Ingredients
03/28/2014 Food Recall

Nova Products, Inc. of Aston, Pennsylvania is voluntarily recalling the following products: African Black Ant (Lot# 2006-000926), Black Ant (Lot# 2006-3627878), XZen Gold (Lot# 130310GL), ZXen Platinum (Lot# 130520PL), XZen 1200 (Lot# 13051012), XZone Gold (Lot# 131110GL), and XZone 1200 (Lot# 13071012) at the retail level. Lot numbers are identified on the back or side of each product. FDA laboratory analysis on these products has determined that they contain undeclared amounts of sildenafil and tadalafil, active ingredients of FDA-approved drugs used to treat erectile dysfunction.

  • Company:
    Nova Products, Inc.
  • Problem
    Entanglement Hazard
Alli (60 mg orlistat capsules) by GlaxoSmithKline: Recall - Product Tampering
03/28/2014 Medical Recall

Some packages of the product were tampered with and may contain product that is not authentic.

  • Company:
    Alli
Glaxosmithkline Recalls Alli®
03/28/2014 Food Recall

laxoSmithKline (GSK) Consumer Healthcare is voluntarily recalling all alliĀ® weight loss products from U.S. and Puerto Rico retailers as the company believes that some packages of the product were tampered with and may contain product that is not authentic alliĀ®. GSK is conducting an investigation and is working with the knowledge of the U.S. Food and Drug Administration (FDA) on this retailer level recall.

  • Company:
    GlaxoSmithKline
  • Problem
    Fall Hazard And Risk Of Serious Injury
Macadamia Nut Allergy Alert and Voluntary Recall of 15-Count Boxes of Chocolate Chunk LUNA Bars Due to Package Mislabeling
03/28/2014 Food Recall

Clif Bar and Company is initiating a voluntary recall today of a small amount of 15-count boxes of Chocolate Chunk LUNA Bars that were shipped to limited stores nationwide. These 15-count boxes include Chocolate Chunk LUNA Bars made with macadamia nut butter, but the wrappers do not include macadamia nuts in the ingredient list or allergen statement.

  • Company:
    Clif Bar & Company
  • Problem
    Due To Particulate Matter