In October of 1982, Tylenol, the leading pain-killer
medicine in the United States at the time, faced a tremendous crisis when seven people in Chicago were reported dead after taking extra-strength Tylenol capsules. It was reported that an unknown suspect/s put 65 milligrams of deadly cyanide into Tylenol capsules, 10,000 more than what is necessary to kill a human. The tampering occurred once the product reached the shelves. They were removed from the shelves, infected with cyanide and returned to the shelves . In 1982, Tylenol controlled 37 percent of its market with revenue of about $1.2 million. Immediately after the cyanide poisonings, its market share was reduced to seven percent. Johnson & Johnson Decision Making Once the connection was made between the Tylenol capsules and the reported deaths, public announcements were made warning people about the consumption of the product. Following the guidelines of protecting people first and property second. *Conducted an immediate product recall from the entire country which amounted to about 31 million bottles and a loss of more than $100 million dollars.
*Although Johnson & Johnson knew they were not
responsible for the tampering of the product, they assumed responsibility by ensuring public safety first and recalled all of their capsules from the market. Johnson & Johnson re-introduce the product to the market with the help of their decision making Once the product was removed from the market, Johnson & Johnson had to come up with a campaign to reintroduce its product and restore confidence back to the consumer. 1. Tylenol products were re-introduced containing a triple-seal tamper resistant packaging. 2. In order to motivate consumers to buy the product, they offered a $2.50 off coupon on the purchase of their product. They were available in the newspapers as well as by calling a toll-free number. 3. To recover loss stock from the crisis, Johnson & Johnson made a new pricing program that gave consumers up to 25% off the purchase of the product.