FDA Devices recall · Reported May 9, 2018
Specimen Gate Screening Center, Part Number 5002-0500, All software versions from 1.0 to 1.8 (current software version) Specimen Gate Screening Center is used for data management of neonatal screening test results and demographics by qualified laboratory personnel in newborn screening programs.
Potential errors in patient results generated by the Screening Center product that include both false negative and false positive results.
PerkinElmer Life and Analytical Sciences, Wallac, Oy recalled Specimen Gate Screening Center, Part Number 5002-0500, All software versions from 1.0 to … - a moderate-severity action.
Specimen Gate Screening Center, Part Number 5002-0500, All software versions from 1.0 to … was recalled by PerkinElmer Life and Analytical Sciences, Wallac, Oy in May 9, 2018. Reason: Potential errors in patient results generated by the Screening Center product that include both false negativ…. Check the official notice for the remedy. Verify recall #Z-1541-2018 with the FDA Devices before acting.
The recall
PerkinElmer Life and Analytical Sciences, Wallac, Oy issued this moderate-severity FDA Devices recall-Potential errors in patient results generated by the Screening Center product that include both false negativ….
- Moderate
- severity level
- 8 units
- affected scope
- Class II
- classification
- May 9, 2018
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1541-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) 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, 6 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 - 41,021 medical devices recalls on record
Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. 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.
Product description
Specimen Gate Screening Center, Part Number 5002-0500, All software versions from 1.0 to 1.8 (current software version) Specimen Gate Screening Center is used for data management of neonatal screening test results and demographics by qualified laboratory personnel in newborn screening programs.
Reason for recall
Potential errors in patient results generated by the Screening Center product that include both false negative and false positive results.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-1541-2018 |
| Date reported | May 9, 2018 |
| Date initiated | November 17, 2017 |
| Recalling firm | PerkinElmer Life and Analytical Sciences, Wallac, Oy |
| Firm location | Turku, N/A |
| Affected scope | 8 |
| Distribution | Worldwide Distribution - US Distribution to the state of Georgia., and to the countries of : Belgium, Canada, Denmark, Italy, and 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-1541-2018) 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.
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Nationwide recalls with similar severity or category timing
Drug and device notices outside this firm and state, matched by severity timing and product category.
Similar severity · nearest report date
Same archive severity grade (Moderate), closest by report date among other firms and states.
Similar Medical Devices · nearest report date
Same product category, closest by report date among other firms and states (deduped against the severity set).
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Methodology · Corrections · Archive as of August 2026