[Recalled] Perkin Elmer Genetic Screening Processor (GSP) Product Code: 2021-0010 Product Usage: The GSP instrument is a fully automated, high throughput batch analyzer for time- resolved and prompt fluorescence analysis of samples in
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | Perkin Elmer Genetic Screening Processor (GSP) Product Code: 2021-0010 Product Usage: The GSP instrument is a fully automated, high throughput batch analyzer for time- resolved and prompt fluorescence analysis of samples in microtitration plates. It is intended for in vitro quantitative / quali |
|---|---|
| Brand / manufacturer | Perkinelmer |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2121-2012 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 27 June 2012 |
| EAN / barcode | 20210001 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Contamination from GSP Shaker unit results in decreased signal activity of assay measurements for Genetic Screening for Neonatal IRT, TSH and IRT
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Perkinelmer
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.