Skip to content
Recall Observatory FDA recall evidence

Device product

Ferno PROFlexx¿ Model 28Z Chair Cot

Z-1827-2017

March 08, 2017

Class II

Product summary

Firm
Ferno-Washington Inc
Event
Event 76765
Status
Terminated
Classification
Class II
Quantity
34 units
Official record key
device-enforcement:Z-1827-2017

Official wording

Reason: The recall was initiated as a result of the detection of an incorrect nut used in manufacturing.

Code information: 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

Distribution pattern: Worldwide distribution. The recalled products were distributed to the following states: CA, FL, HI, IL, NY, OH. There are no government accounts for this recall. There are no Canada accounts for this recall. There are no Mexico accounts for this recall. The recalled product was distributed to the following countries: Taiwan, United Arab Emirates, Thailand, Singapore

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    The recall was initiated as a result of the detection of an incorrect nut used in manufacturing.