Luminex Corporation Recall: VERIGENE Enteric Pathogens Nucleic Acid Test, Part No. 30-002-
Luminex Corporation Recall: VERIGENE Enteric Pathogens Nucleic Acid Test, Part No. 30-002- is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Luminex Corporation; Product: VERIGENE Enteric Pathogens Nucleic Acid Test, Part No. 30-002-23; Reason for recall: There is a potential for false n
| Recalling firm | Luminex Corporation |
|---|---|
| Product | VERIGENE Enteric Pathogens Nucleic Acid Test, Part No. 30-002-23 |
| Reason for recall | There is a potential for false negative results using VERIGENE CDF Stool PREP KIT and VERIGENE EP Stool PREP KIT due to hydrophobic characteristics of the swab. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Ongoing |
| Distribution | Worldwide distribution - US Nationwide and the countries of Kuwait, Austria, France, Greece, Kuwait, Turkey. |
| Recall initiated | 20220617 |
| Recall number | Z-1335-2022 |
| Category | device |
| State | IL |
| Country | United States |
$29/mo
Try RecallGuard →