Otsuka America Pharmaceutical, Inc. Recalls

FDA
1
Total Recalls
1
Agencies
Feb 2011
First Recall
Feb 2011
Latest Recall

Showing 1-1 of 1 recalls

FDA

UBiT-IR300 Infrared Spectrophotometer, Software Versions 7.0, 7.01 and 7.11.

Medical device power supply may overheat and cause smoke to be emitted from the device.

The initial distributor in the US notified consignees 03/14/08 and 03/26/08 by letter. Consignees were provided two different letters depending on the hours of use of the spectrophotometer. The notifications advised of the firm's preventive service and upgrade program for the instrument's power supply, in which consignees would receive a temporary replacement instrument while the service is completed. Consignees with spectrophotometers having <15000 light source hours were notified similarly, and were provided filters and instructions for cleaning and replacing the filters to protect the power supply from unnecessary accumulation of debris. Contact firm at 1-888-MERETEK for assistance.