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Ossur Announces Voluntary Recall of Certain Models of the Total KneeDate: 4/3/2006
Reason: Some units of the Total Knee device may contain faulty pins based in the axis of the knee.
Distribution: Nationwide.
WASHINGTON , D.C. - The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed. Ossur hf. (ICEX: OSSR) today announced a voluntary worldwide recall of the 1100, 1900, 2000 and 2100 models of its Total Knee prosthetic device. The company's initiation of the recall, effective immediately, is based on a finding that some units of the Total Knee device may contain faulty pins based in the axis of the knee. At this time, there have been no incidents or injuries resulting from this situation that have been reported to the company. To date, the incidence of actual product failures within the recalled knees is less than one percent (1%). The serial numbers of the affected knees, which were ordered from June 7th, 2005 to present, have been identified. The In addition, Ossur has temporarily suspended sales and shipments of Total Knees until further notice. To expedite this process in the consideration of both its customers and patients, the implementation of a replacement program will be effective immediately. "We take the issue of patient safety very seriously," said Jon Sigurdsson, president and chief executive officer of Ossur. "We instituted this recall immediately, upon learning of the faulty pins, because we believe that the patient's wellbeing is our first priority. In addition, we are taking measures to guarantee the quality and safety of the replacement knees." Ossur has informed the U.S. Food and Drug Administration and regulatory authorities in other countries of its decision to implement this recall. Ossur will continue to provide regular and frequent updates as more information becomes available. You may also access the company website at www.ossur.com for this information, in real time. If you have additional questions, you may contact Ossur at the following numbers: Other Drugs / Medicines Recalls and Alerts of InterestDate: 8/7/2008 Reason: These lots represent an illegally marketed drug containing an undeclared ingredient. Distribution: Nationwide Date: 6/12/2008 Reason: Taking AZASAN® instead of SOLODYN® presents a health hazard and safety risk to patients Date: 8/7/2008 Reason: A sample from one lot of the product revealed that it contained a potentially harmful undeclared ingredient, thio-methisosildenafil. Distribution: Nationwide Date: 8/7/2008 Reason: The product contains potentially harmful, undeclared ingredients. Distribution: Nationwide Date: 6/12/2008 Reason: Limited lots of Atrium heparin-coated Hydraglide Thoracic Catheters were manufactured with heparin found to have been contaminated with oversulfated chondroitin sulfate (OSCS) Distribution: Nationwide Date: 7/16/2008 Reason: A sample from product lot 856396A tested positive for a strain of yeast, which could potentially affect immunocompromised patients. Distribution: Nationwide |
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