Drug recall
BuckyDiagnost Ceiling System (Stitching Patient Support) 704031
FDA recall event 80577 · Class II · Philips Medical Systems Gmbh, DMC
Key facts
| Event ID | 80577 |
|---|---|
| Recall numbers | Z-2841-2018, Z-2842-2018, Z-2843-2018, Z-2844-2018, Z-2845-2018, Z-2846-2018, Z-2847-2018, Z-2848-2018, Z-2849-2018, Z-2850-2018, Z-2851-2018, Z-2852-2018 and 16 more |
| Recalling firm | Philips Medical Systems Gmbh, DMC |
| Product type | Devices |
| Products | BuckyDiagnost Ceiling System (Stitching Patient Support) 704031, CombiDiagnost R90 (Stitching Patient Support) 709030, DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712081, DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712082, DigitalDiagnost 4.1 Chest / Emergency (Stitching Patient Support) 712029 and 18 more |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| 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. |
| Initiation date | Jun 27, 2018 |
| Report date | Aug 29, 2018 |
| Termination date | Apr 30, 2024 |
| City | Hamburg |
| Country | Germany |
| FEI number | 3003768251 |
At a glance
- 10–99 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: