[Recalled] Verigene Processor SP, Model Numbers: 10-0000-07 and 10-0000-07-R — Two of three complaints were initiated due to the customers repeatedly obtainin… | FDA 2019-04-22
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | Verigene Processor SP, Model Numbers: 10-0000-07 and 10-0000-07-R |
|---|---|
| Brand / manufacturer | Luminex Corporation |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0920-2022 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 22 April 2019 |
| EAN / barcode | 13042054 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Two of three complaints were initiated due to the customers repeatedly obtaining No Call results on the Processor SPs in question.
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 Luminex Corporation
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.