Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported November 15, 2017
NucliSENS Lysis Buffer Extended lot for RES 76675
Elute may become colored due to the residual presence of heme group origination from hemoglobin present in whole blood samples as well as dried spot (DBS) samples. This can poten…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
BioMerieux Sa recalled NucliSENS Lysis Buffer Extended lot for RES 76675 - a moderate-severity action.
NucliSENS Lysis Buffer Extended lot for RES 76675 was recalled by BioMerieux Sa in November 15, 2017. Reason: Elute may become colored due to the residual presence of heme group origination from hemoglobin present in wh…. Check the official notice for the remedy. Verify recall #Z-0086-2018 with the FDA Devices before acting.
The recall
BioMerieux Sa issued this moderate-severity FDA Devices recall-Elute may become colored due to the residual presence of heme group origination from hemoglobin present in wh….
- Moderate
- severity level
- 911 units
- affected scope
- Class II
- classification
- November 15, 2017
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0086-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0086-2018) was formally reported on November 15, 2017, with the manufacturer initiating the action on October 18, 2017. It is classified under Moderate severity (Class II), with a current status of Terminated. BioMerieux Sa is listed as the recalling firm, operating out of Marcy L'Etoile, N/A. Federal records list the affected scope as 911 units.
The documented reason for this recall is: Elute may become colored due to the residual presence of heme group origination from hemoglobin present in whole blood samples as well as dried spot (DBS) samples. This can potentially cause the inhibition of PCR react… Distribution data in the federal record shows the product reached: Distributed domestically to MD, CO, and OH.. 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 - 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 - 40,422 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
911 units
Related Recalls
6
0 from same agency
Product description
NucliSENS Lysis Buffer Extended lot for RES 76675
Reason for recall
Elute may become colored due to the residual presence of heme group origination from hemoglobin present in whole blood samples as well as dried spot (DBS) samples. This can potentially cause the inhibition of PCR reactions and result in an uninterpretable test result. If using an Internal Control (IC) in the extraction process the IC could potentially be inhibited as well and invalidate test results.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-0086-2018 |
| Date reported | November 15, 2017 |
| Date initiated | October 18, 2017 |
| Recalling firm | BioMerieux Sa |
| Firm location | Marcy L'Etoile, N/A |
| Affected scope | 911 units |
| Distribution | Distributed domestically to MD, CO, and OH. |
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-0086-2018) 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? ▼
NucliSENS Lysis Buffer Extended lot for RES 76675. Recalled by BioMerieux Sa. Units affected: 911 units.
Why was this product recalled? ▼
Elute may become colored due to the residual presence of heme group origination from hemoglobin present in whole blood samples as well as dried spot (DBS) samples. This can potentially cause the inhibition of PCR reactions and result in an uninterpretable test result. If using an Internal Control (IC) in the extraction process the IC could potentially be inhibited as well and invalidate test results.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 15, 2017. Severity: Moderate. Recall number: Z-0086-2018.
Where was the recalled product distributed? ▼
Distribution: Distributed domestically to MD, CO, and OH..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0086-2018) 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 November 15, 2017. 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.