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Richard Wolf Medical Instruments Corp. recalls Reuseable rotary blade/abrader, product number 899751504. The oval burr laterally hooded is an attachment or accessory
Recalled February 17, 2016 · FDA recall Z-0790-2016 · Richard Wolf Medical Instruments
Hazard
Weak weld in the reusable rotary blade/abrader (burr) may result in inner part breaks at the distal or proximal end making the product dysfunctional. · FDA Class II
Units
four units
Sold at
Distributed in Washington.
Description
Weak weld in the reusable rotary blade/abrader (burr) may result in inner part breaks at the distal or proximal end making the product dysfunctional.
Product
Reuseable rotary blade/abrader, product number 899751504. The oval burr laterally hooded is an attachment or accessory to the air-powered device intended for use during surgical procedures to cut hard tissue or bone and soft tissue. General hospital and plastic surgery use.
Manufacturer(s)
Richard Wolf Medical Instruments Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →