Diamedix Corporation Recall: Diamedix Is-EBV-VCA IgG Test Kit Diamedix Is-Mumps IgG Test K
Diamedix Corporation Recall: Diamedix Is-EBV-VCA IgG Test Kit Diamedix Is-Mumps IgG Test K is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Diamedix Corporation; Product: Diamedix Is-EBV-VCA IgG Test Kit Diamedix Is-Mumps IgG Test Kit is an EIA procedure intended for the qualitative and
| Recalling firm | Diamedix Corporation |
|---|---|
| Product | Diamedix Is-EBV-VCA IgG Test Kit Diamedix Is-Mumps IgG Test Kit is an EIA procedure intended for the qualitative and semi-quantitative detection of Mumps IgG antibodies as an aid in the diagnosis of Mumps infection. |
| Reason for recall | A gel-like substance was found in kit component, sample diluent , that could potentially compromise product performance. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Worldwide distribution: US nationwide including states of: AZ, CA, CO, FL, GA, IL, IN, KY, MA, MI, MO, NC, NE, NH, NJ, NY, OH, OK, OR, PA, RI, TN, TX, VA, WI and Puerto Rico. and Country of: ITALY. |
| Recall initiated | 20141020 |
| Recall number | Z-1686-2016 |
| Category | device |
| State | FL |
| Country | United States |
$29/mo
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