Philips MR systems: Trolley Variable Height IRF — Class II medical device recall Z-1827-2014
Terminated recall by Philips Medical Systems, Inc., reported 2014-06-25, distributed nationwide. Ingenia customers have experienced clamping of the foot under the central column of the Height Adjustable Flex
| Recall number | Z-1827-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips Medical Systems, Inc., Andover, MA, United States |
| Recall initiated | 2014-05-15 |
| Classified | 2014-06-18 |
| Reported by FDA | 2014-06-25 |
| Terminated | 2015-08-07 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AT, AU, BG, BR, CA, CH, CN, DE, DK, EE, ES, FI, FR, GB, GR, IT, JO, KR, MX, NL, NO, NZ, OM, PK, SE, SG, SK, TH, TR, TW, VN, ZA |
| Quantity | 5 |
| Model numbers | 030, 1929.1, 9896 |
Product
Philips MR systems: Trolley Variable Height IRF (for Ingenia 1.5T & 3.0T products) Product Usage: Diagnostic MR System. The Height Adjustable FlexTrak trolley and Trolley Variable Height IRF is an optional device designed to prepare the patient outside the examination room to enhance workflow and make additional non-magnetic hospital beds unnecessary.
Reason for recall
Ingenia customers have experienced clamping of the foot under the central column of the Height Adjustable Flex Trak trolley and the Trolley Variable Height IRF.
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-1827-2014. 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.