The Maestro System 204-503, Straight Permucosal Ext, 5mm x 3mm
FDA device recall Z-0925-05 · posted 2005-06-23 · Terminated
Recall details
- Recalling firm
- BioHorizons Implant Systems Inc
- Reason for recall
- The product labeled as a Straight Permucosal Ext, 5mm x 3mm contained a profile abutment for Cement.
- Action taken
- The domestic consignees were contacted by telephone on 06/03/2005 to request the return of the products. The foreign consignee was contacted via telephone and email to request the same action.
- Root cause
- Other
- Status
- Terminated
- Product code
- NDP
- Quantity affected
- 5 units
- Distribution
- PA, TX, MI, VA and Russia
- Date initiated
- 2005-06-03
- Date posted
- 2005-06-23
- Date terminated
- 2005-08-11
- Location
- Birmingham, AL
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