FDA Medical Device Recalls (openFDA)
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.
- Recall number
- Z-2953-2011
- Recalling firm
- International Technidyne Corp.
- Product
- 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.
- Status
- Terminated
- Initiated
- 2011-05-10
- Posted
- 2011-08-05
- Terminated
- 2012-11-02
- Reason
- Certain lots of Hemochron Jr. PT Cuvettes (J201) demonstrate a higher bias than historically observed when compared to laboratory reference instruments.
- Root cause
- Device Design
- Action
- International 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.
- Quantity
- 6,218 boxes in US ; 4713 boxes outside US
- Distribution
- Worldwide 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, Qatar, Saudi Arabia, Sweden, Turkey, Taiwan, and South Africa.
- Lot, serial or model codes
- Catalogue/Code J201 Lot Number: FOJPT059, GOJPT067, GOJPT068, GOJPT069, GOJPT070, GOJPT072, GOJPT073, GOJPT074, GOJPT075, HOJPT076, HOJPT077, HOJPT078, HOJPT079, HOJPT080, HOJPT081, HOJPT082, HOJPT083, JOJPT084, JOJPT085, JOJPT086, JOJPT087, JOJPT088, JOJPT090, KOJPT091, KOJPT092, KOJPT093, MOJPT094, MOJPT095, MOJPT096, MOJPT097, MOJPT098, MOJPT099, A1JPT001, A1JPT002 A1JPT003 A1JPT005 A1JPT007 A1JPT008, A1JPT009, A1JPT010, A1JPT011, A1JPT012, A1JPT013, A1JPT014, A1JPT015, A1JPT016, A1JPT017, A1JPT018, A1JPT019, A1JPT021, A1JPT023, A1JPT024, A1JPT025, B1JPT032, B1JPT033, C1JPT035, C1JPT038, C1JPT041, and C1JPT045.
- 510(k) numbers
- ["K940432","K974799"]
- PMA numbers
- not on file
- Product code
- JPA
- Firm FEI
- 1000526865
- Firm city
- Edison
- Firm state
- NJ
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28