Gram Negative Identification Panel
FDA adverse event reports and recall history for gram negative identification panel (product code LQM), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 377
- Deaths
- 2
- Injuries
- 12
- Malfunctions
- 363
Reports per year
Source: FDA adverse event reports by year received, 2000–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Recent recalls
- 2023-01-04Open, ClassifiedStorage
VITEK 2 REAGENT GN TEST KIT VTK2 20 CARDS, CATALOG 21341
As the temperature and time out of range was exceeded, product performances cannot be guaranteed
- 2017-05-22TerminatedPackaging
VITEK 2 Gram-Negative identification card (GN), IVD, REF 21341, 20 cards per carton.
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
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