Ferno Model 35X PROFlexx Stretchers — Class II medical device recall Z-0995-2015
Terminated recall by Ferno-Washington Inc, reported 2015-01-28, distributed in GA, HI, MA, MO, NJ, OH, TN, TX. The wheel castor assemblies may be loosening on the stretchers.
| Recall number | Z-0995-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ferno-Washington Inc, Wilmington, OH, United States |
| Recall initiated | 2014-12-03 |
| Classified | 2015-01-16 |
| Reported by FDA | 2015-01-28 |
| Terminated | 2015-12-01 |
| Distributed | GA, HI, MA, MO, NJ, OH, TN, TX |
| Countries outside the US | CA, DE, VE |
| Quantity | 46 units |
| Model numbers | 35X |
Product
Ferno Model 35X PROFlexx Stretchers, one unit per package
Reason for recall
The wheel castor assemblies may be loosening on the stretchers.
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-0995-2015. 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.