Recall Z-1827-2017— Ferno-Washington Inc
Class II · Terminated
Class II FDA medical device recall by Ferno-Washington Inc, initiated 2017-03-08, terminated 2017-06-29. FDA's recall record names no specific 510(k) clearance for this event. 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..
- Recalling firm
- Ferno-Washington Inc
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2017-03-08
- Terminated
- 2017-06-29
- Firm location
- Wilmington, OH, United States
Product description
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.