Fischer Imaging Corporation Bloom DTU-215-B Programmable Stimulator Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Bloom DTU-215-B Programmable Stimulator
Brand
Fischer Imaging Corporation
Lot Codes / Batch Numbers
All Bloom DTU-215-B Programmable Stimulators.
Products Sold
All Bloom DTU-215-B Programmable Stimulators.
Fischer Imaging Corporation is recalling Bloom DTU-215-B Programmable Stimulator due to Possibility that after a loss of power or brown-out, the device may transmit unintended stimulation to patients.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Possibility that after a loss of power or brown-out, the device may transmit unintended stimulation to patients.
Recommended Action
Per FDA guidance
Customers were notified by letter on 01/13/05.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026