Ferno PROFlexx¿ Model 28Z Chair Cot — Class II medical device recall Z-1827-2017
Terminated recall by Ferno-Washington Inc, reported 2017-04-26, distributed in CA, FL, HI, IL, NY, OH. The recall was initiated as a result of the detection of an incorrect nut used in manufacturing.
| Recall number | Z-1827-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ferno-Washington Inc, Wilmington, OH, United States |
| Recall initiated | 2017-03-08 |
| Classified | 2017-04-15 |
| Reported by FDA | 2017-04-26 |
| Terminated | 2017-06-29 |
| Distributed | CA, FL, HI, IL, NY, OH |
| Countries outside the US | AE, CA, MX, SG, TH, TW |
| Quantity | 34 units |
| Model numbers | 28Z |
Product
Ferno PROFlexx¿ Model 28Z Chair Cot
Reason for recall
The recall was initiated as a result of the detection of an incorrect nut used in manufacturing.
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-1827-2017. 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.