Drug recall
Cepheid, Sample Collection Device, Part: 900-0370
FDA recall event 94932 · Class II · Cepheid
Key facts
| Event ID | 94932 |
|---|---|
| Recall numbers | Z-2584-2024 |
| Recalling firm | Cepheid |
| Product type | Devices |
| Products | Cepheid, Sample Collection Device, Part: 900-0370 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Specimen collection device may leak after the patient sample swabs have been inserted into the test tubes, which could result in biohazard exposure, cross contamination causing false positive results… |
| Initiation date | Jun 20, 2024 |
| Report date | Aug 21, 2024 |
| City | Sunnyvale |
| State | CA |
| Country | United States |
| FEI number | 3004530258 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: