Vertical Spring Arm for Single or Dual Monitor Mount — Class II medical device recall Z-1850-2014
Terminated recall by Steris Corporation, reported 2014-07-02, distributed in MA, NY, OH, PA, TX. Potential for the welded seam in affected monitor spring arms to crack and/or break.
| Recall number | Z-1850-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Steris Corporation, Mentor, OH, United States |
| Recall initiated | 2014-04-04 |
| Classified | 2014-06-23 |
| Reported by FDA | 2014-07-02 |
| Terminated | 2014-10-15 |
| Distributed | MA, NY, OH, PA, TX |
| Countries outside the US | CA |
| Quantity | 68 units |
| Reason classes | packaging, device malfunction |
| UPC / GTIN / UDI-DI | 00011106337525 |
| Serial numbers | 01108340587, 011106337516, 011106337525, 011106337527, 011106337534, 011106337535, 011106337538, 011106337539, 011106337541, 011106337626, 011107338878, 011107338882, 011107338883, 0111073388883, 011108340587, 011108340600, 011108340600A, 01117338881, ART00001, ART00010, CADS0001, CADS0015, CBX0001, CBX0010, CXSG0008 and 1 more |
| Model numbers | YG19051, YG19262 |
Product
Vertical Spring Arm for Single or Dual Monitor Mount (Harmony LL 500 and Harmony LL 700 surgical lighting systems), Steris Corporation. Model numbers YG19051 and YG19262.
Reason for recall
Potential for the welded seam in affected monitor spring arms to crack and/or break.
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-1850-2014. 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.