FDA Medical Device Recalls (openFDA)
Roche Diagnostics Corp.: CoaguChek Plus meter; catalog # 475729 and 12816001.
- Recall number
- Z-0814-03
- Recalling firm
- Roche Diagnostics Corp.
- Product
- CoaguChek Plus meter; catalog # 475729 and 12816001.
- Status
- Terminated
- Initiated
- 2003-03-12
- Posted
- 2003-05-14
- Terminated
- 2005-02-03
- Reason
- High frequency signals from other medical or communications equipment will result in a variable positive bias in test results.
- Root cause
- Other
- Action
- Urgent Product Removal letters dated 3/12/03 were sent to all customers. Distributors were asked to conduct a recall from their customers. Replacement meters are not currently available from Roche. Roche will temporarily provide a CoaguChek S system to run PT samples and will reimburse for APTT and ACT tests that are sent to an accredited outside laboratory.
- Quantity
- 472
- Distribution
- United States
- Lot, serial or model codes
- All units
- 510(k) numbers
- ["K860719"]
- PMA numbers
- not on file
- Product code
- JPA
- Firm FEI
- 1823260
- Firm city
- Indianapolis
- Firm state
- IN
- 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