GE Healthcare, LLC Recall: Precision 500D
GE Healthcare, LLC Recall: Precision 500D is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: GE Healthcare, LLC; Product: Precision 500D; Reason for recall: GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige S
| Recalling firm | GE Healthcare, LLC |
|---|---|
| Product | Precision 500D |
| Reason for recall | GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | US: AL, AR, AZ, CA, CO, CT, DC, FL, GA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT,NC, NE NH, NJ, NM, NY, NV, OH, OK, PA, RI, SC, SD, TN, TX,, VA, WA, WO, WY, WV. OUS: Algeria Armenia Australia Austria Brazil Canada Chile China Denmark Egypt France Germany Guatemala Honduras Hong Kong Hungar |
| Recall initiated | 20161121 |
| Recall number | Z-0910-2017 |
| Category | device |
| State | WI |
| Country | United States |
$29/mo
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