Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported January 1, 2014
Instrument Manager driver : Driver sysu100i that connects to the Sysmex UF-100 analyzer Software all versions prior to( v7.00.0006 and v8.00.0005): v7.00.0001, v7.00.0002, v7.00.0003, v7.00.0004, v7.00.0005, v8 .00.0001, v8.00.0002, v8.00.0003, and v8 .00.0004
When connected to the Sysmex UF-100, the Instrument Manager driver sysu100i driver software versions 7.00.0001, 7.00.0002, 7.00.0003, 7.00.0004, 7.00.0005, 8.00.0001, 8.00.0002, …
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Data Innovations, Inc. recalled Instrument Manager driver : Driver sysu100i that connects to the Sysmex UF-100 analyzer … - a moderate-severity action.
Instrument Manager driver : Driver sysu100i that connects to the Sysmex UF-100 analyzer … was recalled by Data Innovations, Inc. in January 1, 2014. Reason: When connected to the Sysmex UF-100, the Instrument Manager driver sysu100i driver software versions 7.00.00…. Check the official notice for the remedy. Verify recall #Z-0571-2014 with the FDA Devices before acting.
The recall
Data Innovations, Inc. issued this moderate-severity FDA Devices recall-When connected to the Sysmex UF-100, the Instrument Manager driver sysu100i driver software versions 7.00.00….
- Moderate
- severity level
- Class II
- classification
- January 1, 2014
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0571-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0571-2014) was formally reported on January 1, 2014, with the manufacturer initiating the action on November 6, 2013. It is classified under Moderate severity (Class II), with a current status of Terminated. Data Innovations, Inc. is listed as the recalling firm, operating out of South Burlington, VT. Federal records list the affected scope as 24 systems.
The documented reason for this recall is: When connected to the Sysmex UF-100, the Instrument Manager driver sysu100i driver software versions 7.00.0001, 7.00.0002, 7.00.0003, 7.00.0004, 7.00.0005, 8.00.0001, 8.00.0002, 8.00.0003, and 8.00.0004, and is config… Distribution data in the federal record shows the product reached: Nationwide Canada and Britain. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
24 systems
Related Recalls
6
3 from same agency
Product description
Instrument Manager driver : Driver sysu100i that connects to the Sysmex UF-100 analyzer Software all versions prior to( v7.00.0006 and v8.00.0005): v7.00.0001, v7.00.0002, v7.00.0003, v7.00.0004, v7.00.0005, v8 .00.0001, v8.00.0002, v8.00.0003, and v8 .00.0004
Reason for recall
When connected to the Sysmex UF-100, the Instrument Manager driver sysu100i driver software versions 7.00.0001, 7.00.0002, 7.00.0003, 7.00.0004, 7.00.0005, 8.00.0001, 8.00.0002, 8.00.0003, and 8.00.0004, and is configured with option "Strip Zeros from Result" set to "Yes" may result in sample error
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-0571-2014 |
| Date reported | January 1, 2014 |
| Date initiated | November 6, 2013 |
| Recalling firm | Data Innovations, Inc. |
| Firm location | South Burlington, VT |
| Affected scope | 24 systems |
| Distribution | Nationwide Canada and Britain |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-0571-2014) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Instrument Manager driver : Driver sysu100i that connects to the Sysmex UF-100 analyzer Software all versions prior to( v7.00.0006 and v8.00.0005): v7.00.0001, v7.00.0002, v7.00.0003, v7.00.0004, v7.00.0005, v8 .00.0001, v8.00.0002, v8.00.0003, and v8 .00.0004. Recalled by Data Innovations, Inc.. Units affected: 24 systems.
Why was this product recalled? ▼
When connected to the Sysmex UF-100, the Instrument Manager driver sysu100i driver software versions 7.00.0001, 7.00.0002, 7.00.0003, 7.00.0004, 7.00.0005, 8.00.0001, 8.00.0002, 8.00.0003, and 8.00.0004, and is configured with option "Strip Zeros from Result" set to "Yes" may result in sample error
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on January 1, 2014. Severity: Moderate. Recall number: Z-0571-2014.
Where was the recalled product distributed? ▼
Distribution: Nationwide Canada and Britain.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0571-2014) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported January 1, 2014. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.