The Anspach Effort, Inc. Product is Anspach eMax Drill System console, catalog numbers SC-1000 and SC-1000-1 (does not include the related drill motor, foot-pedal control, motor attachments or drills/burrs) Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Product is Anspach eMax Drill System console, catalog numbers SC-1000 and SC-1000-1 (does not include the related drill motor, foot-pedal control, motor attachments or drills/burrs)
Brand
The Anspach Effort, Inc.
Lot Codes / Batch Numbers
Serial Numbers: 50139962-2, 50128299-4, 50139968-5, 50139963-5, 50116580-5, 50128299-5, 50139964-2, 50139962-1, 50139971-2, 50139968-1, 50139964-3, 50128295-2, 50139964-1, 50139968-2, 50139964-4, 50128299-3, 50116576-2, 50128299-2, 50139968-3, 50139963-2, 50139968-4, 50139963-4, 114766-1, 114766-2
Products Sold
Serial Numbers: 50139962-2, 50128299-4, 50139968-5, 50139963-5, 50116580-5, 50128299-5, 50139964-2, 50139962-1, 50139971-2, 50139968-1, 50139964-3, 50128295-2, 50139964-1, 50139968-2, 50139964-4, 50128299-3, 50116576-2, 50128299-2, 50139968-3, 50139963-2, , 50139968-4, 50139963-4, 114766-1,114766-2
The Anspach Effort, Inc. is recalling Product is Anspach eMax Drill System console, catalog numbers SC-1000 and SC-1000-1 (does not inclu due to Faulty component causing a malfunction which would unexpectedly shutdown the drill system and user may not be able to restart.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Faulty component causing a malfunction which would unexpectedly shutdown the drill system and user may not be able to restart.
Recommended Action
Per FDA guidance
A recall notification letter was mailed to domestic consignees and faxed to international consignees on April 23, 2003. The letter requests return of the devices.
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 noticeDistribution
As reported by FDA
CA, FL, GA, IN, MA, MS, NC, TX
Page updated: Jan 10, 2026