FDA Medical Device Recalls (openFDA)
Soft Computer Consultants, Inc.: SoftGenomics version 4.1.15.6 SoftGenomics is a laboratory workflow and information management system to be used in a clinical molecular or cytogenetics laboratory or medical research laboratory setting by knowledgeable and trained users. SoftGenomics is used to record and track activities performed in ordering, specimen processing (pre-analytical steps), testing, documentation, and reporting.
- Recall number
- Z-2093-2021
- Recalling firm
- Soft Computer Consultants, Inc.
- Product
- SoftGenomics version 4.1.15.6 SoftGenomics is a laboratory workflow and information management system to be used in a clinical molecular or cytogenetics laboratory or medical research laboratory setting by knowledgeable and trained users. SoftGenomics is used to record and track activities performed in ordering, specimen processing (pre-analytical steps), testing, documentation, and reporting.
- Status
- Terminated
- Initiated
- 2021-03-31
- Posted
- not on file
- Terminated
- 2022-04-15
- Reason
- Software showing wrong results reported, PDF not match HIS.
- Root cause
- Software Design Change
- Action
- The firm sent an " URGENT: MEDICAL DEVICE RECALL" letter dated 6/2/2021 to its sole consignee of the correction on 06/02/2021 by mail. The letter described the product, problem and actions to be taken. The consignee was instructed to do the following: Acknowledge receipt of this letter in the TMS task Give permission to load Hot Fix on Test environment Perform validation activities to completion Acknowledge Hot Fix has been moved to Live environment and is working as expected Type of action by Company: All clients on affected lines of software have been notified of the recall. SCC will provide Hot Fixes for all affected lines that will be delivered to all affected clients. Until the software correction is delivered, clients have been informed of an alternative workflow to avoid the problem. The firm provided information on a software update performed on 03/31/2021 and stated that, "Hot Fix has already been delivered." If you have any further questions, Please call 1-800-763-8522 (Technical Support 24/7).
- Quantity
- 1
- Distribution
- US Distribution to: CA only
- Lot, serial or model codes
- Version 4.1.15.6
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- JQP
- Firm FEI
- 1000307651
- Firm city
- Clearwater
- Firm state
- FL
- 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