Philips Medical Systems Gmbh, DMC Recall: DigitalDiagnost Dual Detector (Stitching Patient
Philips Medical Systems Gmbh, DMC Recall: DigitalDiagnost Dual Detector (Stitching Patient is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Philips Medical Systems Gmbh, DMC; Product: DigitalDiagnost Dual Detector (Stitching Patient Support) 712022; Reason for recall: The hook does not
| Recalling firm | Philips Medical Systems Gmbh, DMC |
|---|---|
| Product | DigitalDiagnost Dual Detector (Stitching Patient Support) 712022 |
| Reason for recall | The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | US Nationwide; International to 66 countries |
| Recall initiated | 20180627 |
| Recall number | Z-2858-2018 |
| Category | device |
| Country | Germany |
$29/mo
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