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Johnson & Johnson looks to rebuild consumer confidence after 11 recalls

Johnson & Johnson’s CEO Bill Weldon said Friday he knows the company let consumers down with 11 recalls of medicines, contact lenses and hip implants in 11 months.

Associated Press (2007)

Johnson & Johnson’s CEO Bill Weldon said Friday he knows the company let consumers down with 11 recalls of medicines, contact lenses and hip implants in 11 months.

TRENTON, N.J. — With Johnson & Johnson's once-golden reputation tarnished by 11 recalls of medicines, contact lenses and hip implants in as many months, its chief executive says he knows the company let consumers down.

J&J plans a public campaign to help rebuild their trust, but not until after about 40 recalled nonprescription medicines are back on store shelves sometime early next year. In the meantime, the company is also doing everything possible "to make sure this never happens again," CEO Bill Weldon said Friday.

The maker of trusted brands including Johnson's No More Tears baby shampoo, Tylenol pain reliever and Neosporin antibiotic ointment has announced repeated recalls since late last September. Nine involved nonprescription medicines — from Children's Benadryl to Tylenol Arthritis — made by its McNeil Consumer Healthcare unit.

The biggest was an astounding April 30 recall of 136 million bottles of children's and infants' liquid medicines that might have contained tiny metal particles or have too much active ingredient.

"We've learned a lot of lessons. They've been very painful," Weldon said.

No serious injuries have been linked to any recalled products.

But Congress, federal prosecutors and the Food and Drug Administration's Office of Criminal Investigation are looking into the handling of the recalls, including a "stealth" one in 2008 in which J&J allegedly paid a third party to secretly pull Motrin packets with questionable potency off store shelves. All this from the company almost revered for its honesty and caution when an unknown perpetrator laced Tylenol bottles with cyanide in Chicago in 1982.

This week was particularly bad for the world's biggest health-products maker. J&J received a warning from the Food and Drug Administration about illegal marketing of some hip implants and two more recalls: one involving two other hip implant products and one involving contact lenses sold in Asia and Europe that stung some users' eyes.

Asked if he can assure consumers there won't be any more recalls, Weldon said, "I don't think you can ever say 'never' to anything."

"We're doing everything we can anyplace in Johnson & Johnson to make sure this never happens again," he added.

Last week, J&J appointed a new quality director who will report directly to Weldon and oversee three "chief quality officers," one each for J&J's consumer products, prescription drug and medical device businesses.

Asked whether members of the board of directors have pressed Weldon, the board's chairman, for more aggressive action or even his resignation, he said board discussions are not public.

The Associated Press called the other 10 board members, but all either declined to comment, were unavailable or did not return messages.

Al Ries, chairman of Atlanta marketing consultants Ries & Ries, said that given J&J's "unprecedented" 11 recalls, it will take time for people to forget about the problems, but they will, eventually.

"If I were the CEO, I would call a special board meeting and I would resign," Ries said, adding that if the board did not agree, the CEO should propose major internal changes.

Some of recalled products

Recalled on Aug. 26:

• ASR Hip Resurfacing System

(ball portion of hip), sold only outside U.S.

• ASR XL Acetabular System

(socket part of the pelvis)

Recalled on Aug. 23:

• 1 Day Acuvue TruEye contact lenses sold in Japan, other countries in Asia and Europe

Recalled on July 8:

• 21 lots of Benadryl, Children's Tylenol, Motrin IB, Tylenol Extra Strength, Tylenol

Day & Night, and Tylenol PM

Recalled on June 15:

• Tylenol Extra Strength Rapid Release

Gelcaps, 50 count

• Benadryl Allergy Ultratab, 100 count

Recalled on April 30:

• Concentrated Tylenol Infants' Drops,

7 sizes or flavors

• Children's Benadryl Allergy

Recalled on March 31:

• Zyrtec Itchy Eye Drops, 0.17 oz.

Recalled on Jan. 15:

• Children's Tylenol Meltaways, 2 versions

• Motrin IB, 13 versions

Consumers who bought recalled

McNeil products may request a refund or a coupon for a future purchase

at mcneilproductrecall.com

Johnson & Johnson looks to rebuild consumer confidence after 11 recalls 08/27/10 [Last modified: Friday, August 27, 2010 10:04pm]
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