Ferno-Washington Inc: Medical Device Recall in 2017 - (Recall #: Z-1827-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Ferno PROFlexx¿ Model 28Z Chair Cot

Product Classification:

Class II

Date Initiated: March 8, 2017

Date Posted: April 26, 2017

Recall Number: Z-1827-2017

Event ID: 76765

Reason for Recall:

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

Status: Terminated

Product Quantity: 34 units

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

Voluntary or Mandated:

Voluntary: Firm initiated