FDA Announces Class I Recall of Certain Infusion Set Needles
FDA Announces Class I Recall of Certain Infusion Set Needles
The U.S. Food and Drug Administration today announced a Class I recall of Exel/Exelint Huber needles, Exel/Exelint Huber Infusion Sets and Exel/Exelint Securetouch+ Safety Huber Infusion Sets, manufactured by Nipro Medical Corporation for Exelint International Corporation.
Hettich Centrifuges with 2050 and 2076 Plastic Rotors: Recall
Plastic centrifuge rotor may crack, break apart and be forcefully ejected.