Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

DA-2006P - Defibrillator / Pacer Analyzer Recalled by BC Group International Inc Due to Device is not functioning as intended: Two wires...

Date: October 28, 2015
Company: BC Group International Inc
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 BC Group International Inc directly.

Affected Products

DA-2006P - Defibrillator / Pacer Analyzer; Product Usage: Intended to measure the output of a defibrillator or transcutaneous pacemaker.

Quantity: 5 units

Why Was This Recalled?

Device is not functioning as intended: Two wires running to the ECG distribution circuit board are reversed resulting in inverted waveforms.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About BC Group International Inc

BC Group International Inc has 1 total recall tracked by RecallDetector.

Related Recalls

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