FDA Medical Device Recalls (openFDA)
Medishop USA: OneTouch/Basic/Profile Blood Glucose Test Strips, 50 Test Strips per box. Part Number 020-848, LIFESCAN, a Johnson & Johnson company. (The product is labeled in English, Greek and Portuguese)
- Recall number
- Z-0207-2007
- Recalling firm
- Medishop USA
- Product
- OneTouch/Basic/Profile Blood Glucose Test Strips, 50 Test Strips per box. Part Number 020-848, LIFESCAN, a Johnson & Johnson company. (The product is labeled in English, Greek and Portuguese)
- Status
- Terminated
- Initiated
- 2006-10-17
- Posted
- 2006-12-08
- Terminated
- 2008-07-16
- Reason
- Counterfeit-(manufacturer unknown)
- Root cause
- Other
- Action
- The recalling firm faxed, e-mailed and/or mailed ''Urgent Medical Device'' letters and response forms (dated 10/17/06) to the 5 distributor accounts.
- Quantity
- 7,727 boxes (50 strips per box)
- Distribution
- Worldwide Distribution-including the states of NY, NJ, MS and country of Canada
- Lot, serial or model codes
- Lots 2606340, 2619932, 272894A; Part # 020-848.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- NBW
- Firm FEI
- 3003666334
- Firm city
- not on file
- Firm state
- NY
- 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