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Roche Diagnostics Issues a Worldwide Voluntary Recall of Some of its ACCU-CHEK Aviva MetersDate: 1/18/2006
Reason: The potential for an electronic malfunction which can cause the meter to report an erroneous result or shut down and no longer be used.
Distribution: Nationwide.
The Food and Drug Administration (FDA) released the following information: Roche Diagnostics has initiated a worldwide voluntary recall of specific Accu-Check Aviva Meters because of the potential for an electronic malfunction which can cause the meter to report an erroneous result or shut down and no longer be used. The recall includes U.S. serial numbers 52500000000 through 52510999999. Outside the U.S., the recall includes serial numbers 52600000000 through 52610999999, 52700000000 through 52710999999, and 52800000000 through 52810999999. Customers outside the U.S. have also been notified. Roche Diagnostics launched the ACCU-CHEK Aviva meter in the U.S. in August of 2005. It is estimated that there are 150,000 ACCU-CHEK Aviva meters with these serial numbers currently in the U.S. market, and that only these recalled ACCU-CHEK Aviva meters have the potential to experience this electronic malfunction. To date, 3 customer meter malfunctions have been confirmed in the U.S., in relation to this issue and 5 outside the U.S.. The FDA and foreign governments have been apprised of this voluntary recall. Accu-Chek Aviva meters were distributed to wholesale and retail distributors throughout the U.S. They can be identified by reviewing the serial number located on the back of the meter. If the serial number falls within the range of 52500000000 through 52510999999, it is potentially affected and therefore subject to this recall. Roche Diagnostics has notified its distributors and registered customers in the U.S. by mail and is arranging for replacement of the recalled products. In the U.S., consumers with general questions may contact the ACCU-CHEK Customer Care Service Center at 1-800-858-8072 and health care professionals may contact the ACCU-CHEK Customer Care Service Center at 1-800-440-3638. Other Drugs / Medicines Recalls and Alerts of InterestDate: 6/12/2008 Reason: Oversized tablets may contain as much as two times the labeled level of active morphine sulfate 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: 6/16/2008 Reason: Oversized tablets may contain as much as two times the labeled level of active morphine sulfate Distribution: Nationwide Date: 6/12/2008 Reason: Taking AZASAN® instead of SOLODYN® presents a health hazard and safety risk to patients Date: 6/12/2008 Reason: Limited lots of Carmeda-coated products were manufactured with heparin found to have been contaminated with oversulfated chondroitin sulfate (OSCS). Distribution: Nationwide Date: 6/12/2008 Reason: it contained a potentially harmful undeclared ingredient, hydroxyhomosildenafil Distribution: Nationwide |
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