Primus Corporation Recall: Ultra2 Resolution Variants System for Abnormal Hemoglobin Quant
Primus Corporation Recall: Ultra2 Resolution Variants System for Abnormal Hemoglobin Quant is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Primus Corporation; Product: Ultra2 Resolution Variants System for Abnormal Hemoglobin Quantitation; Reason for recall: The product did not receive
| Recalling firm | Primus Corporation |
|---|---|
| Product | Ultra2 Resolution Variants System for Abnormal Hemoglobin Quantitation |
| Reason for recall | The product did not receive pre-market approval or clearance. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | US - Arizona, California, District of Columbia, Florida, Georgia, Illinois, Louisiana, Massachusetts, Michigan, Missouri, Nebraska, New Jersey, Nevada, New York, Pennsylvania, Rhode Island, Tennessee, Texas, Virginia, Wisconsin OUS - Bahrain, Iran, Malaysia, Saudi Arabia, Taiwan, Turkey, UAE, UK, Vi |
| Recall initiated | 20201009 |
| Recall number | Z-0321-2021 |
| Category | device |
| State | MO |
| Country | United States |
$29/mo
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