Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Pro Time Microcoagulation System/ Pro Time 3 Cuvette Recalled by International Technidyne Corp. Due to Some Pro Time3 Test Cuvettes within a specified...

Date: September 28, 2012
Company: International Technidyne Corp.
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact International Technidyne Corp. directly.

Affected Products

Pro Time Microcoagulation System/ Pro Time 3 Cuvette, Pro3-4, Pro3-25, and Pro3-50. International Technidyne Corporation. The Pro Time Microcoagulation System is a portable battery operated instrument with a disposable cuvette for quantitative determination of prothrombin time from fingerstick whole blood or anticoagulant free venous whole blood.

Quantity: 11,742 boxes US (25 cuvettes per box); 22,968 boxes OUS (25 cuvettes per box)

Why Was This Recalled?

Some Pro Time3 Test Cuvettes within a specified lot range may recover lower than expected Prothrombin Time/International Normalized Ratio (PT/INR) results.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About International Technidyne Corp.

International Technidyne Corp. has 1 total recall tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report