Philips TraumaDiagnost- a Stationary X-Ray System — Class II medical device recall Z-1806-2020
Terminated recall by Philips North America, LLC, reported 2020-05-06, distributed nationwide. If the shaft breaks due to material fatigue, the trauma arm can fall down and may result in injury.
| Recall number | Z-1806-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips North America, LLC, Andover, MA, United States |
| Recall initiated | 2020-04-07 |
| Classified | 2020-04-28 |
| Reported by FDA | 2020-05-06 |
| Terminated | 2023-04-28 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, AU, CA, DE, FR, GB, GR, HU, IE, NL, PT, SI |
| Model numbers | 720013 |
Product
Philips TraumaDiagnost- a Stationary X-Ray System (Bucky System) Model: 720013 - Product Usage: general radiography.
Reason for recall
If the shaft breaks due to material fatigue, the trauma arm can fall down and may result in injury.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1806-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.