An online report published on Monday, February 24 revealed that Fitbit voluntarily recalled its fitness tracker the Force wristband over reports of skin irritation on February 20.
Fitbit CEO James Park said in a statement that almost 2% of Force wristband users experienced skin irritation. He further stated that the rashes might be the skin’s adverse reaction to certain substances found in the product’s strap or adhesives.
The company also announced it has created a website for users who want to return the Force wristband for reimbursement.
Our legal team at the Law Offices of Paul Levin has years of experience serving Connecticut residents who have been harmed by a defective product such as this. If you too have been suffering from an injury or harm as a result of a defective product, call us at (860) 560-7226 to discuss the possibility of filing a legal claim.
One lot of 5% dextrose injection and four lots of 0.9% sodium chloride injection have been voluntarily recalled by Baxter International Inc. on December 27 after the company found that its intravenous solutions are contaminated with particulate matter, which may potentially cause blood vessel obstruction.
IV solutions being recalled were distributed in the United States between May 2012 and October 2013. Lots being recalled are:
- 5% Dextrose Injection (100 mL) with Lot No. P285288 (Code: 2B0089)
- 0.9 % Sodium Chloride Injection (50 mL) with Lot No. P297283 (Code: 2B1308)
- 0.9 % Sodium Chloride Injection (100 mL) with Lot No. P292326 (Code: 2B1302)
- 0.9 % Sodium Chloride Injection (100 mL) with Lot No. P293993 (Code: 2B1302)
- 0.9 % Sodium Chloride Injection (100 mL) with Lot No. P293514 (Code: 2B1309)
Our lawyers from the Law Offices of Paul Levin are ready to help Connecticut residents who have been injured by defective products such as these. Call us at 860.560.7226 to know how we can help you possibly file a lawsuit.