Cardiocommand recalls TAPSYSTEM Model : 2A units with specific serial numbers due to potential battery wire connection error affecting power switch.
There is a potential for an assembly error resulting in the battery wire being connected to the ON/OFF power switch incorrectly.
Cardiocommand is recalling TAPSYSTEM Model 2A devices with serial numbers 2197A through 2201A because of a possible assembly error that could connect the battery wire incorrectly to the power switch. This issue might cause the device to malfunction or fail to turn off properly.
The assembly error could cause the battery wire to be connected incorrectly to the ON/OFF power switch. This might lead to the device failing to turn off properly or malfunctioning, but it does not pose an immediate risk of serious injury.
Users of the TAPSYSTEM Model 2A with serial numbers 2197A through 2201A are affected. Those who use the device for medical purposes may be at slightly higher risk due to potential malfunction.
Check your TAPSYSTEM Model 2A device for serial numbers 2197A, 2196A, 2198A, 2199A, 2200A, or 2201A. These specific serial numbers are part of the recall.
Look for the serial number on your TAPSYSTEM Model 2A device to confirm if it is in the recall list (2197A, 2196A, 2198A, 2199A, 2200A, or 2201A).
Cardiocommand recalls TAPSYSTEM Model 2A units with specific serial numbers due to a potential assembly error that could connect the battery wire incorrectly to the ON/OFF power switch.
Check your device's serial number to see if it is in the recall list (2197A, 2196A, 2198A, 2199A, 2200A, or 2201A). If it is, you should contact Cardiocommand for further instructions.
The recall states there is a potential for assembly error, but it does not indicate a risk of serious injury. The hazard is considered low risk.
We’ve drafted a message you can send Cardiocommand to request your refund or repair — edit it as you like.
Subject: Recall Z-1976-2019 — Cardiocommand Cardiocommand Hello, I own a Cardiocommand that is covered by recall Z-1976-2019 from Cardiocommand. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
