Siemens Healthcare Diagnostics, Inc. Recall: APTIO RACK INPUT MODULE
Siemens Healthcare Diagnostics, Inc. Recall: APTIO RACK INPUT MODULE is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Siemens Healthcare Diagnostics, Inc.; Product: APTIO RACK INPUT MODULE; Reason for recall: The modules may have been shipped without a warning label for potential risk o
| Recalling firm | Siemens Healthcare Diagnostics, Inc. |
|---|---|
| Product | APTIO RACK INPUT MODULE |
| Reason for recall | The modules may have been shipped without a warning label for potential risk of interference to pacemaker functionality. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | The products were distributed to the following US states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, PA, SC, TN, TX, VA, WA, and WV. The products were distributed to the following foreign countries: Australia, Austria, |
| Recall initiated | 20180814 |
| Recall number | Z-0210-2019 |
| Category | device |
| State | NY |
| Country | United States |
$29/mo
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