Johnson and Johnson Product Recalled, Orthopedic Device--LPS Diaphyseal Sleeve--Poses Serious Malfunction

Johnson and Johnson-the company known for its gentle baby shampoos and other caring products-has received a negative response from the U.S. Food and Drug Administration (FDA) for one of its products.

The FDA said it notified healthcare professionals of a Class I recall, the most serious kind, of an orthopedic device made by the company.

LPS Diaphyseal Sleeve, a product made by Johnson and Johnson used for reconstructive knee surgery, has been recalled because of potential fractures.

According to Reuters, the agency has received 10 reports of incidents in which the device has malfunctioned. (That's not very caring of you, J & J.)

The affected devices were manufactured by Depuy, Johnson and Johnson's orthopedic unit from 2008 to July 20, 2012.

A recall like this one could mean serious problems for the company. For instance, a fracture in the sleeve at the joint of the product could lead to loss of function or loss of a limb, infection, compromised soft tissue or death, according to the FDA.

The FDA said the company is not recommending revision or additional follow up in the absence of symptoms of patients with this implanted device.

However, as Johnson and Johnson Depuy is defending itself against a slew of lawsuits over its hip implants, one thing's for certain-we'll certainly be a little hesitant about buying the loving companies goodies, especially for our little ones and even more so, now, for our elderly. And sadly, this isn't the first time the company has recalled products for reasons ranging from harmful chemicals in Tylenol to choking hazards.