Pfizer Recalls 1 Million Packages of Birth Control
Pfizer Inc. is recalling fourteen lots of Lo/Ovral-28 tablets and 14 lots of its generic brands Norgestrel and Ethinyl Estradiol. The recall has been issued after Pfizer discovered that some packages of birth control had too many active pills while others had to few. The packaging error is estimated to have affected one million packages of birth control packages. Patients relying on any of the affected birth control packets are encouraged to use alternative contraceptives, as this month's packet may not be effective.
Oral contraceptives work by increasing hormone levels with active pills for 21 days, followed by 7 days of placebo pills. A woman taking a sugar pill out of order may not have enough contraceptive in their body to prevent a pregnancy. Please take the following steps to determine whether your packet has been recalled:
- Make sure you have been prescribed Lo/Ovral or Norgestrel and Ethinyl Estradiol birth control pills. Other brands have not been affected by this recall.
- Check the expiration dates. The recalled packets have expiration dates between July 31, 2013 and March 31, 2014.
- Double check to see the lot number of your packet matches the lot numbers of the recalled birth control pills on FDA's Pfizer recall page.
For more information regarding your rights after an unintentional pregnancy, please contact our Pfizer recall attorneys to schedule a free consultation. Our California product liability lawyers will assess your case and help you determine your eligibility to file a product liability suit.
The listeria outbreak responsible for deaths and illnesses across 26 states has now risen to 25 and 123 respectively, US News reported. According to the CDC, the states in which the effects of listeria caused the deaths of many individuals include Colorado, Indiana, Kansas, Louisiana, Maryland, Missouri, Nebraska, New Mexico, New York, Oklahoma, Texas, and Wyoming. Those who have died in this tragic incident were between the ages of 48- and 96-years-old. The number of deaths and illnesses that have grown within the past few months became the country's most deadliest outbreak in 25 years.
According to KTVU News, the listeria outbreak involving the contaminated cantaloupes is now responsible for 21 deaths. The Centers for Disease Control and Prevention reported new deaths in Indiana, New York, and Wyoming. The CDC also indicated that 109 people in numerous states from California to the East Coast have sustained illnesses in the outbreak.
DENVER, COLORADO -- According to USA Today, the cantaloupe listeria outbreak that resulted in deaths and serious illnesses to individuals throughout the United States was traced to Jensen Farms in Holly, Colorado. The company recalled the "Rocky Ford" brand cantaloupes earlier this month, however, the Food and Drug Administration found listeria in cantaloupes from grocery stores in the state of Colorado and from a victim's home that were grown at Jensen Farms. Investigators also found matching listeria strains, which were located on the equipment and cantaloupes at Jensen Farms' packing facility.
Qualitest Pharmaceuticals, which is an entity of Endo Pharmaceuticals Holdings Inc., has recalled more than a million packages of defectively packaged birth control pills. The voluntary recall, which takes effect immediately, was issued because of a packaging error that may inadvertently cause women to take the incorrect dose of birth control and consequently, put women at risk for an unplanned pregnancy. In a statement released by the U.S. Food and Drug Administration (FDA), multiple lots of birth control pill blister packs were rotated 180 degrees, which resulted in the reversal of the daily regimen. The rotation also hid the lot number and expiration date. According to the FDA, there are no immediate health risks associated with the error, but women taking the affected pills are being told to use a non-hormonal form of birth control immediately and consult a health care provider.
Toyota announced a recall of 80,000 Hybrid sport utility vehicles Wednesday, June 29th. According to a 10 News report, the recall includes 2006 and 2007 models of the Highlander Hybrid and Lexus RX 400h sold in the U.S. According to the automaker, some models contain faulty electronics systems that may cause the vehicle's hybrid drive system to fail. Toyota is working on obtaining the necessary replacement parts and once the parts are available, owners will be notified of the recall by first class mail in mid-July 2011. Detailed information on the recall can be found on the
According to the Orange County Register, McNeil Consumer Healthcare, a subsidiary of Johnson & Johnson, issued a recall for more than 60,000 bottles of Tylenol Extra Strength Tablets. The product is being pulled from store shelves because of a musty odor caused by a chemical called TBA, which is a byproduct of a preservative in shipping palettes. The odor has caused minor cases of nausea and anyone who has bought the product should stop using it immediately. The product was manufactured in February 2009 and has a lot number of ABA619 and a UPC number of 300450444271. Anyone who has had an adverse reaction to the medicine should contact the
Unilever United States, the manufacturer of Skippy Peanut Butter, has recalled two of its products sold in 16 different states after a routine testing indicated salmonella may be present. According to a
PISMO BEACH - A 37-year-old Visalia man was killed Saturday when he was thrown from a Yamaha Rhino UTV at the Oceano Dunes State Vehicular Recreation Area. The March 5th accident happened just before 1:30 p.m. at the Sand Highway Marker 13 area. The victim, Jose Lopez, Jr., was riding a Yamaha Rhino that overturned. Lopez died of his injuries at the scene. Another passenger was unharmed. According to the Fresno Bee, the state Department of Parks and Recreation is the primary agency investigating the accident.
Honda is recalling 2,277 vehicles to replace a wiring coupler on some models. The vehicles affected include the 2010 Honda Accord and the 2010 Honda CR-V equipped with the four-cylinder powertrain. According to USA Today, the coupler may have been damaged during assembly, which could lead to engine stalling. Owners will receive notification in February, and Honda says it will replace the wire harness coupler at no cost. So far, no injuries or accidents have been reported. For more information, Honda owners can go to
The Associated Press reported today that Salsa Cycles, a unity of Quality Bicycle Products, has voluntarily recalled 6,500 bicycle handle stems due to a defect, which can cause the stems to crack or break, posing a fall hazard to riders.
Twenty-one children were hurt in May 2008 when the spinning Yo-Yo chair ride collapsed at the Calaveras County Fair. After a 10-month investigation, the California Department of Industrial Relations determined the ride had not been properly maintained, saying a damaged washer failed to hold a pair of nuts in place, causing the arms to crash.
In product recall news, the United Stated Consumer Product Safety Commission (CPSC), in cooperation with Easton Sports, based out of Scotts Valley, CA, has announced a recall of about 200 2010 EC90 Zero seat posts. According to the CPSC, the EC90 Zero seat posts are black with red and gray graphics. "EC90" is printed on the post. The carbon top clamp of the seat post can crack, posing a fall hazard to the rider. The bicycles were sold at Turner Suspension Bicycles, Ibis Cycles and Security Bicycle Accessories retailers nationwide from April 2010 through August 2010 for between $150 and $200. Consumers who own a bicycle with the recalled seat post are urged to contact Easton Sports toll-free at (866) 892-6059 between 8 a.m. and 5 p.m. CT Monday through Friday or visit the firm's website at 
