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Product Recalls

Simmons Kids Crib Mattresses

Kid Crib mattresses smaller than the 27 1/4 minimum width requirement are an entrapment hazard to infants because of the gap between the mattress and crib rails. The following mattresses were recalled on June 5, 2008 by the U.S. Consumer Product Safety Commission because they were smaller than the minimum width requirement:

• Pottery Barn Kids by Simmons Kids Lullaby
• Simmons Kids Slumber Time Evening Star Luxury Firm
• Simmons Kids Baby Mattress Series 400
• Simmons Kids Baby Mattress 234 Coil Count

Owners of these mattresses should measure their width and contact Simmons Kids to receive a free replacement mattress if the mattresses are less than 27 1/4 inches. Please visit www.simmonskids.com or call 1-800-810-8611.

Other recent product recalls include:

Munire Furniture
• Majestic Curved Top cribs with model number 9500
• Majestic Flat Top cribs with model number 9000
• Essex cribs with model number 7100
• Brighton/Sussex cribs with model number 9100
• Captiva cribs with model number 5100.

Polaris Industries
• 2006 OUTLAW 500 "IRS"
• 2007 OUTLAW 500 "IRS"
• 2007 OUTLAW 525 "IRS"
• 2008 OUTLAW 525 "IRS"

Recaro Child Safety Car Seat
• Signo and Como Convertible Child Restraint Systems

Simplicity Inc.
• Nursery-in-a-Box cribs

These products were recalled due to defects which might cause harm to the user or others around the product. Even pharmaceutical products have been recalled by the manufacturers. Pharmaceutical products are by nature thought to be safe and effective for their intended use. It is assumed that all necessary testing has been done by the pharmaceutical company before the product is released for use. If the pharmaceutical product has defects or is contaminated or does not contain warnings about possible adverse effect, it amounts to negligence on the part of the manufacturer.

Bayer Trasylol Recall

Trasylol is used to reduce perioperative blood loss and the need for blood transfusion in patients undergoing cardiopulmonary bypass in the course of coronary artery bypass graft surgery who are at an increased risk for blood loss and blood transfusion. Trasylol is most commonly given to patients undergoing cardiopulmonary bypass, a procedure that enables a machine to take over the heart’s function when it is stopped during surgery, during coronary artery bypass graft surgery, a medical procedure used to increase blood flow to the heart. Trasylol is administered to patients who are at an increased risk for blood loss and potential blood transfusion.

Trasylol was recalled amid growing evidence that the drug may be linked to a higher risk of death than that of competing drugs. Trasylol had been linked to increased risk of death, kidney or renal failure, heart attacks, strokes and encephalopathy among heart surgery patients.

If you or any of your family member has suffered from a product which has been recalled, contact the Georgia injury lawyers at The Burnside Firm . Our team of attorneys can help you get the compensation you deserve. We represent injury victims throughout Georgia from our offices in Athens GA. Contact us for a free initial consultation. Don’t loose out on the compensation you deserve. Call 1-800-569-1937

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