Reported Jul 24, 2019 · Terminated

TAPSYSTEM Model 2A, REF 8002A

Cardiocommand Inc.

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Cardiocommand Inc. · 4920 W Cypress St Ste 110 · Tampa, FL · 33607-3837

Is this the product you have?

    • TAPSYSTEM Model 2A
    • REF 8002A
Lot codes and dates
  • SERIAL NUMBERS
    • 2197A
    • 2196A
    • 2198A
    • 2199A
    • 2200A
    • and 2201A
Amount recalled
6 units

Where it was sold

Why it was recalled

There is a potential for an assembly error resulting in the battery wire being connected to the ON/OFF power switch incorrectly.

This product is unlikely to cause harm, but it breaks a safety or labelling rule.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Cardiocommand Inc. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Apr 1, 2021 · Data as of Sep 19, 6:19 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.