FDAClass IIIJuly 24, 2019

Tapsystem recall

TAPSYSTEM Model 2A, REF 8002A

Why was Tapsystem recalled?

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

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

SERIAL NUMBERS: 2197A, 2196A, 2198A, 2199A, 2200A, and 2201A,

Product
TAPSYSTEM Model 2A, REF 8002A
Recalling firm
Cardiocommand Inc.
Quantity
6 units
Distribution
United States - AR, NM, PA, TX, and WA.
Recall date
July 24, 2019
Classification
Class III
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls