Recall Classification: Class I Date Recall Initiated: December 23, 2009 Product Names: * Exel Huber Needles * EXELint Huber Needles * Exel Huber Infusion Sets * EXELint Huber Infusion Sets * Exel "Securetouch+" Huber Safety Sets * EXELint Huber Safety Sets ALL LOT NUMBERS BEGINNING WITH 07, 08, OR 09 ARE AFFECTED BY THIS … [Read more...]

FDA Announces Class I Recall of Certain Infusion Set Needles Huber needles used in implanted ports to withdraw blood, inject medications, and other solutions 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 … [Read more...]

Hettich Centrifuges, Beverly, MA, is initiating a North America and Canada recall of 2050 and 2076 plastic hematocrit rotors that are used in combination with the Mikro 12-24, Mikro 20, Haematokrit 20 and Haematokrit 24 bench top plastic centrifuges. These plastic rotors have the potential to break apart resulting in pieces of the rotor to be … [Read more...]

Nipro Medical Corporation, Miami FL, is initiating a nationwide recall of all GlucoPro Insulin Syringes (This does not include the GlucoPro syringe specific for use with the Amigo Insulin pump). These syringes may have needles that detach from the syringe. If the needle becomes detached from the syringe during use, it can become stuck in the … [Read more...]

MuscleMaster.com is recalling all lots and expiration dates of the seventeen below listed dietary supplements sold between June 1, 2009 and November 17, 2009. FDA informed MuscleMaster.com that it believes that the Recalled Products contain ingredients that are steroids. Specifically, FDA advised MuscleMaster.com of its concern that the Recalled … [Read more...]