FDAMarch 6, 2025device
Pacific Hemostasis Thromboplastin-D, 4 ml. Used in performing one-stage prothrombin time test and factor assays.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
The incorrect value of the International Sensitivity Index (ISI) is printed on the outer box label.
What to do
FDA enforcement status: Ongoing
Brands named
fisher diagnosticsfisher
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDASiemens Dimension Tacrolimus Flex Reagent Cartridge (TAC), REF DF207, SMN 10700795; enzyme immunoassay2026-05-07
- FDAdirectCHECK ACT-LR whole blood quality control, level 2 Model/Catalog Number: DCGLR-22026-04-30
- FDABioFire Joint Infection (JI) Panel REF: RFIT-ASY-0138, 30 test Kit.2026-04-22
- CPSCFree-Standing Professional Gas Ranges Recalled Due to Risk of Burn Hazard; Manufactured by Fisher & Paykel2026-04-16
- FDAepoc BGEM BUN Test Card (25 pk) for the epoc Blood Analysis System; Siemens Material Number (SMN): 10736515;2026-04-02
- FDABiofire Spotfire Respiratory/Sore Throat Panel REF: 4234852026-04-01
- FDADimension Creatinine Flex reagent cartridge. Material Number: 10872079.2026-03-18
- FDALeadCare Ultra Blood Lead Test Kit; Catalog Number: 70-8098; The LeadCare Ultra kit is provided with the following materials: " Sensors (8 containers of 24 each; 192 tests) " Treatment Reagent Tubes (8 containers of 24 each; 192 tests) " Calibration Button (1 @) " Lead Control Level 1 (1 @ 2 mL) ...2026-03-13
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