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Greiner Bio-One North America, Inc. recalls 4 ml FX Sodium Fluoride/Potassium Oxalate tube, Ref 454297 VACUETTE Glycolytic Inhibitor Tubes contain an antiglycolyti
Recalled June 15, 2016 · FDA recall Z-1923-2016 · Greiner Bio-One North America
Hazard
The 4 ml FX Sodium Fluoride/Potassium Oxalate tube may have no or low additive (sodium fluoride and potassium oxalate), which can effect analytical results for glucose and lactate. · FDA Class II
Units
250,800 pieces (209 cases)
Sold at
Nationwide Distribution to CA, FL, IL, KY, NY, PA, VA and Puerto Rico
Description
The 4 ml FX Sodium Fluoride/Potassium Oxalate tube may have no or low additive (sodium fluoride and potassium oxalate), which can effect analytical results for glucose and lactate.
Product
4 ml FX Sodium Fluoride/Potassium Oxalate tube, Ref 454297 VACUETTE Glycolytic Inhibitor Tubes contain an antiglycolytic agent, sodium fluoride, and an anticoagulant, potassium oxalate. The product is suitable for the analysis of blood glucose and lactate
Manufacturer(s)
Greiner Bio-One North America, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →