Sterling Diagnostics, Inc. Recall: Creatinine/Endpoint [Modified Heinegard-Tiderstrom] for
Sterling Diagnostics, Inc. Recall: Creatinine/Endpoint [Modified Heinegard-Tiderstrom] for is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Sterling Diagnostics, Inc.; Product: Creatinine/Endpoint [Modified Heinegard-Tiderstrom] for IN VITRO DIAGNOSTIC USE in the quantitative determinat
| Recalling firm | Sterling Diagnostics, Inc. |
|---|---|
| Product | Creatinine/Endpoint [Modified Heinegard-Tiderstrom] for IN VITRO DIAGNOSTIC USE in the quantitative determination of analytes. These are CONSUMABLES - a customer buys another when kit is consumed. |
| Reason for recall | Sterling Diagnostics, Inc. initiated a recall on 7/20/2016 for multiple diagnostic kits due to a recision of the previously extended expiration dates for the kits. |
| Classification | Class III (least serious — unlikely to cause adverse health consequences) |
| Status | Terminated |
| Distribution | Domestic: MI Foreign: Phillipines VA/DOD: None |
| Recall initiated | 20160720 |
| Recall number | Z-0931-2017 |
| Category | device |
| State | MI |
| Country | United States |
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