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The Anspach Effort, Inc. recalls Rotating Adult Craniotome Product Usage: Pneumatic system
Recalled May 10, 2017 · FDA recall Z-1988-2017 · The Anspach Effort
Hazard
Supplied Directions for Use (DFU) did not contain a recommended service interval. · FDA Class II
Units
49
Sold at
Worldwide Distribution - US Nationwide in the states of HI, DC including PR and the countries of Guam and Japan
Description
Supplied Directions for Use (DFU) did not contain a recommended service interval.
Product
Rotating Adult Craniotome Product Usage: Pneumatic system
Manufacturer(s)
The Anspach Effort, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →