Cardinal Health has issued a recall for the Alaris Infusion Pump model 8100 (also known as the Medley Pump). This recall is due to manufacturing defects. These infusion pumps were used to deliver controlled amounts of medication. The recall applies to devices shipped before September 27, 2007. The recall applies to over 200,000 devices worldwide. The FDA has classified the action as a Class 1 recall, as the use of these pumps involves a reasonable probability of serious injury or death.
We believe the manufacturers failed to warn about the risks associated with these pain pumps and should be held accountable for any harm they have caused. The people who have suffered injuries should be treated fairly and compensated for their losses (whether it is for bills, lost wages, loss of quality of life and independence, or pain and suffering).
If you or a loved one has suffered from Shoulder Pain Management Pumps or Pain Balls after arthroscopic surgery, you may have a claim. We have lawyers dedicated to serve you. Call us today for a free, no obligation consultation. 24 hours a day, 7 days a week. Toll free 1-866-777-2557 or click here for our online contact form.