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FDA Medical Device Recalls (openFDA)

Touch US Llc: etouchus, model no. ETM-G01. Noninvasive Blood glucose meter.

Recall number
Z-1461-2022
Recalling firm
Touch US Llc
Product
etouchus, model no. ETM-G01. Noninvasive Blood glucose meter.
Status
Open, Classified
Initiated
2022-06-21
Posted
not on file
Terminated
not on file
Reason
Device was marketed without FDA 510(k) clearance or a PMA.
Root cause
No Marketing Application
Action
On June 21, 2022, the firm communicated the recall to customers who purchased the product through the company's website. The firm is also making an effort to recall the product that was sold through Amazon Marketplace. Customers should return any affected product to eTouch US LLC. The firm will provide a full refund of the original purchase cost to the customer when the recalled device is received from the customer. If you have any questions, please contact the firm Monday thru Friday, 9AM - 5PM Eastern Time: Support Team: 888-670-9070 Email: Support@etouchus.com
Quantity
149
Distribution
US Nationwide Distribution to: CA, FL IL KY LA MA MD MI NC NH NJ NY OH OK OR PA TN TX VA
Lot, serial or model codes
UDI-DI (GTIN): 00195893740581
510(k) numbers
not on file
PMA numbers
not on file
Product code
NBW
Firm FEI
3023066634
Firm city
Paramus
Firm state
NJ
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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