ClearanceBrief
Recall Z-2953-2011 ยท JPA System, Multipurpose For In Vitro Coagulation Studies

International Technidyne Corp.

Hemochron JR. Microcoagulation Systems Prothrombin Time (PT). International Ethidine Corp (ITC)-Nexus Dx. A unitized mlcrocoagulation test intended for use in performing one-stage prothrombin time.

DateAug 5, 2011 (initiated May 10, 2011)
StatusTerminated
ReasonCertain lots of Hemochron Jr. PT Cuvettes (J201) demonstrate a higher bias than historically observed when compared to laboratory reference instruments.
Root causeDevice Design
ActionInternational Technidyne Corp. (ITC) sent "Urgent Medical Device Recall" letters dated May 10, May 25 and June 09, 2011 to all affected customers. The letter included a description of the problem, asked customers fill out the attached form, and return affected product for replacement. For questions, please contact ITC Technical Support at (800) 631-5945.
Quantity6,218 boxes in US ; 4713 boxes outside US
DistributionWorldwide Distribution: (USA) Nationwide Distribution including the countries of; Austria, Australia, Canada, Switzerland, Germany, Denmark, Estonia, Spain, Finland, France, United Kingdom, Hong Kong, Ireland, Israel, India, Italy, Korea, Liechtenstien, Libya, Netherlands, Norway, Oman,Portugal, Q
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K940432MICROCOAGULATION PROTHROMBIN TIME TEST
International Technidyne Corp., May 18, 1994
K974799HEMOCHRON JR GENERATION II, HEMOCHRON JR SIGNATURE
International Technidyne Corp., Jul 7, 1998