Gentueri Inc recalls
Every recall we track for Gentueri Inc — 2 in all, from 2020–2021 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
2 recalls since 2017.
All FDA recall records for Gentueri Inc since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 1 | 0 | 1 |
| 2021 | 0 | 0 | 1 | 0 | 1 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Gentueri Inc product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Gentueri Inc recalls
2 shown- Lower riskMedical device
Gentueri Inc recalls Gentueri Viral Transport Medium (VTM), Sterile, IVD
Gentueri Inc recalls sterile Viral Transport Medium (VTM) due to potential sample contamination from visual turbidity. Affected lots may cause inaccurate test results.
Gentuer: IncMar 18, 2021 - Lower riskMedical device
Gentueri Inc recalls Gentueri Viral Transport Medium Kit with 8cm Breakpoint Swab
Gentueri Inc recalls Viral Transport Medium Kits with 8cm Breakpoint Swab due to sterility testing failures and contamination evidence. Affected kits may pose infection risks.
Gentuer: IncJul 6, 2020
Gentueri Inc recall questions
How many recalls has Gentueri Inc had?
2 recalls from Gentueri Inc are on record with U.S. safety agencies, from 2020–2021.
What is the most recent Gentueri Inc recall?
Gentueri Inc recalls Gentueri Viral Transport Medium (VTM), Sterile, IVD, dated Mar 18, 2021. Every Gentueri Inc recall is listed on this page, newest first.
What should I do if I have a recalled Gentueri Inc product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Gentueri Inc recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.