FDA Device recall Z-1827-2017
Ferno PROFlexx¿ Model 28Z Chair Cot
- FDA Device
- Class II
- terminated
- Published 2017-04-26
On 2017-04-26 the FDA classified a Class II recall of Ferno PROFlexx¿ Model 28Z Chair Cot by Ferno Washington, citing the recall was initiated as a result of the detection of an incorrect nut used in manufacturing.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1827-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-03-08 |
| Published | 2017-04-26 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ferno Washington |
| Distribution | CA, FL, HI, IL, NY, OH |
Product
Ferno PROFlexx¿ Model 28Z Chair Cot
Reason
The recall was initiated as a result of the detection of an incorrect nut used in manufacturing.
Identifiers
| code_info | 17E003185, 17E003169, 17E003179, 17E003180, 17E003181, 17E003183, 17E003187, 17E003152, 17E003168, 17E003171, 17E003172…17E003185, 17E003169, 17E003179, 17E003180, 17E003181, 17E003183, 17E003187, 17E003152, 17E003168, 17E003171, 17E003172, 17E003173, 17E003184, 17E003170, 17E003138, 17E003139, 17E003140, 17E003141, 17E003153, 17E003154, 17E003155, 17E003156, 17E003157, 17E003158, 17E003159, 17E003160, 17E003161, 17E003162, 17E003163, 17E003164, 17E003165, 17E003166, 17E003167, 17E003174 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1827-2017%22
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