Philips Electronics North America Corporation Recall: AIIuraXperFDlO/10, System Code 72201
Philips Electronics North America Corporation Recall: AIIuraXperFDlO/10, System Code 72201 is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Philips Electronics North America Corporation; Product: AIIuraXperFDlO/10, System Code 722011 Vascular, cardiovascular and neurovascular imaging ap
| Recalling firm | Philips Electronics North America Corporation |
|---|---|
| Product | AIIuraXperFDlO/10, System Code 722011 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions |
| Reason for recall | There is a potential for the Monitor Ceiling Suspension, which holds a large screen monitor, may detach from the actuator rotor shaft causing the monitor to fall from the ground. When a Monitor Ceiling Suspension detaches from the actuator rotor shaft and the monitor falls, there is a risk of injury for the patient, user and bystander. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Worldwide Distribution: US (nationwide) to states of: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, and WY; and countries of: Algeria, Argentina, |
| Recall initiated | 20180716 |
| Recall number | Z-3230-2018 |
| Category | device |
| State | MA |
| Country | United States |
$29/mo
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