Severity
Moderate
ModerateClass IIOngoing
FDA Devices recall · Reported August 21, 2019
ARIES HSV 1&2 Assay , REF 50-10017, UDI # 00840487100295
Through internal investigation, it was discovered that a portion of side cassette assemblies (SCAs) back side seal (BSS) did not meet design specification, resulting in partiall…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Luminex Corporation recalled ARIES HSV 1&2 Assay , REF 50-10017, UDI # 00840487100295 - a moderate-severity action.
ARIES HSV 1&2 Assay , REF 50-10017, UDI # 00840487100295 was recalled by Luminex Corporation in August 21, 2019. Reason: Through internal investigation, it was discovered that a portion of side cassette assemblies (SCAs) back si…. Check the official notice for the remedy. Verify recall #Z-2283-2019 with the FDA Devices before acting.
The recall
Luminex Corporation issued this moderate-severity FDA Devices recall-Through internal investigation, it was discovered that a portion of side cassette assemblies (SCAs) back si….
- Moderate
- severity level
- Class II
- classification
- August 21, 2019
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2283-2019 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-2283-2019) was formally reported on August 21, 2019, with the manufacturer initiating the action on February 20, 2019. It is classified under Moderate severity (Class II), with a current status of Ongoing. Luminex Corporation is listed as the recalling firm, operating out of Austin, TX. Federal records list the affected scope as N/A.
The documented reason for this recall is: Through internal investigation, it was discovered that a portion of side cassette assemblies (SCAs) back side seal (BSS) did not meet design specification, resulting in partially sealed SCAs. The impact of a partial s… Distribution data in the federal record shows the product reached: US: AK, AL, AZ,CA,CO,FL,GA,IL,KS,KY,LA,MA,MD,ME,MI,MN,MO,MS,MT,NC,NE,NJ,NM,NY,OH,ON,OR,PA,TN,TX,UT,VA,VT,WA,WI, OUS: Belgium, Canada, Thailand, Germany, Singapore, United Kingdom. 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
N/A
Related Recalls
6
3 from same agency
Product description
ARIES HSV 1&2 Assay , REF 50-10017, UDI # 00840487100295
Reason for recall
Through internal investigation, it was discovered that a portion of side cassette assemblies (SCAs) back side seal (BSS) did not meet design specification, resulting in partially sealed SCAs. The impact of a partial seal of the BSS could result in potential decrease of volume for each solution in the SCAs and decreased sensitivity or stability of the assay.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | Z-2283-2019 |
| Date reported | August 21, 2019 |
| Date initiated | February 20, 2019 |
| Recalling firm | Luminex Corporation |
| Firm location | Austin, TX |
| Affected scope | N/A |
| Distribution | US: AK, AL, AZ,CA,CO,FL,GA,IL,KS,KY,LA,MA,MD,ME,MI,MN,MO,MS,MT,NC,NE,NJ,NM,NY,OH,ON,OR,PA,TN,TX,UT,VA,VT,WA,WI, OUS: Belgium, Canada, Thailand, Germany, Singapore, United Kingdom |
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-2283-2019) 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? ▼
ARIES HSV 1&2 Assay , REF 50-10017, UDI # 00840487100295. Recalled by Luminex Corporation. Units affected: N/A.
Why was this product recalled? ▼
Through internal investigation, it was discovered that a portion of side cassette assemblies (SCAs) back side seal (BSS) did not meet design specification, resulting in partially sealed SCAs. The impact of a partial seal of the BSS could result in potential decrease of volume for each solution in the SCAs and decreased sensitivity or stability of the assay.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 21, 2019. Severity: Moderate. Recall number: Z-2283-2019.
Where was the recalled product distributed? ▼
Distribution: US: AK, AL, AZ,CA,CO,FL,GA,IL,KS,KY,LA,MA,MD,ME,MI,MN,MO,MS,MT,NC,NE,NJ,NM,NY,OH,ON,OR,PA,TN,TX,UT,VA,VT,WA,WI, OUS: Belgium, Canada, Thailand, Germany, Singapore, United Kingdom.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-2283-2019) 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.
Nearby Recalls in This Category
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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 August 21, 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.