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Terminated

Ferno PROFlexx Model 28Z Chair Cot

FDA Recall Z-1827-2017 · Posted 2017-04-15

Recalling FirmFerno-Washington Inc
Recall StatusTerminated
Product CodeFPO
Date Initiated2017-03-08
Date Terminated2017-06-29
Product Quantity34 units

Reason for Recall

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

Firm Action

Consignees were contacted via telephone and email on 3/8/17. No product will be returned to the recalling firm. The firm and its service company will correct each product in the field at the customers location.

Root Cause

Mixed-up of materials/components

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

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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