Siemens Healthcare Diagnostics, Inc Recall: IMMULITE 2000 Progesterone; Catalog Number: L2
Siemens Healthcare Diagnostics, Inc Recall: IMMULITE 2000 Progesterone; Catalog Number: L2 is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Siemens Healthcare Diagnostics, Inc; Product: IMMULITE 2000 Progesterone; Catalog Number: L2KPW2 L2KPW6; Siemens Material Number: 10381181, 1038117
| Recalling firm | Siemens Healthcare Diagnostics, Inc |
|---|---|
| Product | IMMULITE 2000 Progesterone; Catalog Number: L2KPW2 L2KPW6; Siemens Material Number: 10381181, 10381170 Product Usage: For in vitro diagnostic use with the IMMULITE¿ and IMMULITE 1000 Analyzers - for the quantitative measurement of progesterone in serum as an aid in the diagnosis and treatment of disorders of the ovaries or placenta. |
| Reason for recall | DHEA-S causes falsely elevated progesterone results. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | US Nationwide distribution including Puerto Rico |
| Recall initiated | 20170104 |
| Recall number | Z-1421-2017 |
| Category | device |
| State | MA |
| Country | United States |
$29/mo
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