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Smith & Nephew, Inc., Endoscopy Div. recalls Biosure Ratchet Driver, Product No: 72201888 For delivery and placement of orthopedic screws. Arthroscopic surgical inst
Recalled February 10, 2016 · FDA recall Z-0700-2016 · Smith & Nephew, Inc., Endoscopy Div
Hazard
Driver does not meet specification, oversized. Driver may not be able to be fully inserted into the screw, or screw may become stuck on the driver. · FDA Class II
Units
9
Sold at
Worldwide Distribution - US Distribution to the states of : AK, AL, CA, CO, FL, IL, IN, MI, NE, NJ, NY, OH, OK, PA, SC, TN and TX., and to the countries of : Austria, Australia, Canada, Dubai, Great Britain, India, Italy, Korea, Malaysia, Netherlands, Portugal, Sweden, Switzerland, Singapore and South Africa.
Description
Driver does not meet specification, oversized. Driver may not be able to be fully inserted into the screw, or screw may become stuck on the driver.
Product
Biosure Ratchet Driver, Product No: 72201888 For delivery and placement of orthopedic screws. Arthroscopic surgical instrument
Manufacturer(s)
Smith & Nephew, Inc., Endoscopy Div.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →