Severity
Moderate
ModerateClass IIOngoing
FDA Devices recall · Reported December 4, 2019
V-Twin, REF 6002-800 or 6002-850, SN 18-3304, IVD, (01)03661540600180
During in-house testing it was determined that their is a possibility that during a sample run, the instrument may aspirate a sample from the wrong sample container resulting in…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Vital Scientific N.v. recalled V-Twin, REF 6002-800 or 6002-850, SN 18-3304, IVD, (01)03661540600180 - a moderate-severity action.
V-Twin, REF 6002-800 or 6002-850, SN 18-3304, IVD, (01)03661540600180 was recalled by Vital Scientific N.v. in December 4, 2019. Reason: During in-house testing it was determined that their is a possibility that during a sample run, the instrume…. Check the official notice for the remedy. Verify recall #Z-0547-2020 with the FDA Devices before acting.
The recall
Vital Scientific N.v. issued this moderate-severity FDA Devices recall-During in-house testing it was determined that their is a possibility that during a sample run, the instrume….
- Moderate
- severity level
- Class II
- classification
- December 4, 2019
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0547-2020 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0547-2020) was formally reported on December 4, 2019, with the manufacturer initiating the action on November 15, 2018. It is classified under Moderate severity (Class II), with a current status of Ongoing. Vital Scientific N.v. is listed as the recalling firm, operating out of Dieren. Federal records list the affected scope as 732 instruments.
The documented reason for this recall is: During in-house testing it was determined that their is a possibility that during a sample run, the instrument may aspirate a sample from the wrong sample container resulting in a sample result and patient ID mismatch… Distribution data in the federal record shows the product reached: NY. 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
732 instruments
Related Recalls
6
3 from same agency
Product description
V-Twin, REF 6002-800 or 6002-850, SN 18-3304, IVD, (01)03661540600180
Reason for recall
During in-house testing it was determined that their is a possibility that during a sample run, the instrument may aspirate a sample from the wrong sample container resulting in a sample result and patient ID mismatch. If not detected, this may lead to an incorrect patient report.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | Z-0547-2020 |
| Date reported | December 4, 2019 |
| Date initiated | November 15, 2018 |
| Recalling firm | Vital Scientific N.v. |
| Firm location | Dieren |
| Affected scope | 732 instruments |
| Distribution | NY |
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-0547-2020) 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? ▼
V-Twin, REF 6002-800 or 6002-850, SN 18-3304, IVD, (01)03661540600180. Recalled by Vital Scientific N.v.. Units affected: 732 instruments.
Why was this product recalled? ▼
During in-house testing it was determined that their is a possibility that during a sample run, the instrument may aspirate a sample from the wrong sample container resulting in a sample result and patient ID mismatch. If not detected, this may lead to an incorrect patient report.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 4, 2019. Severity: Moderate. Recall number: Z-0547-2020.
Where was the recalled product distributed? ▼
Distribution: NY.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0547-2020) 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 December 4, 2019. 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.