[Recalled] Dropper Plus Point-of-Care Urinalysis Dipstick Control kit The Quantimetrix Dropper Plus Point-of-Care Urinalysis Dipstick Control is intended as a control for urinalysis reagent strips, microalbumin, and creatinine by the lis
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | Dropper Plus Point-of-Care Urinalysis Dipstick Control kit The Quantimetrix Dropper Plus Point-of-Care Urinalysis Dipstick Control is intended as a control for urinalysis reagent strips, microalbumin, and creatinine by the listed test methods, and as a control for confirmatory tests such as K-CHE |
|---|---|
| Brand / manufacturer | Quantimetrix Corporation |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2257-2018 |
| Country of notice | United States |
| Risk level | Class III |
| Hazard type | recall |
| Notice date | 21 December 2017 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: The kits contained an incorrect lot of Dropper Plus Level 1 vials
This Class III 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 →
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.