Ferno PROFlexx Model 28Z Chair Cot
FDA device recall Z-1827-2017 · posted 2017-04-15 · Terminated
Recall details
- Recalling firm
- Ferno-Washington Inc
- Reason for recall
- The recall was initiated as a result of the detection of an incorrect nut used in manufacturing.
- Action taken
- 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
- Status
- Terminated
- Product code
- FPO
- Quantity affected
- 34 units
- Distribution
- 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
- Date initiated
- 2017-03-08
- Date posted
- 2017-04-15
- Date terminated
- 2017-06-29
- Location
- Wilmington, OH
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