Graco Stroller Recall 2010 – Newell Rubbermaid’s Graco has announced today that they will be voluntarily recalling over 2 million Graco Quattro Tour and MetroLite strollers after the company discovered that 4 babies were killed between between 2003 and 2005.

According to the Consumer Product Safety Commission, the well known baby product manufacturer is pulling the devices of the shelves because it was revealed that infants can accidentally get strapped inside the strollers and be strangled to death.
The baby product company further explained that when kids are not seated and strapped properly into the strollers, they are able to slide through the opening located between the stroller tray and bottom of the seat, where they can get trapped, suffer mild to life threading injuries or be strangled.

The contraption that are being recalled are the Graco Quattro Tour and MetroLite strollers and travel systems with the following codes 8755, 8324, 4600, 8740, 8994, 8676 and 8910.

The hazardous products were available for purchase in 50 states between November 2000 and December 2007.

In late August, 2010, DePuy Orthapedics, a unit of Johnson & Johnson, announced they were recalling two kinds of hip implants. The Food and Drug Administration had received consumer complaints about the hip implants for the last two years. Since 2008, there have been nearly 400 complaints of device failure.

The hip implant failure resulted in patients needing second painful surgeries to replace the first defective hip implant device. It is estimated that around 93,000 people have received the defective hip implant worldwide.

The two recalled DePuy hip implants are the ASR XL Acetabular System, a hip socket replacement and the ASR Hip Resurfacing System, which is a partial hip replacement and puts a metal cap on the ball of the femur. The Acetabular System has been sold all over the world and the resurfacing system has been in use in countries outside of the US.

The ASR hip implants are part of a larger group of medical devices known as metal-on-metal bearings. These devices have known problems generating debris from wear. Some patients develop tissue damage and inflammation as a result.

Last March, the British agency that regulates medical devices issued an advisory about the ASR problems. DePuy began warning doctors about high failure rates in the hip implant the same month the British advisory came out. Prior to this, DePuy claimed they were phasing out the hip implant device due to slow sales.

Failure rates as high as 12 and 13 percent within five years of the patient receiving the medical device were measured. Some doctors and orthopedic experts have expressed dismay that the hip implants were not recalled sooner.

If you or a loved one have been injured as a result of a DePuy hip implant, you should contact our attorneys today.