BioHorizons Implant Systems Inc One Perimeter Park South The Maestro System 204-503, Straight Permucosal Ext, 5mm x 3mm Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
The Maestro System 204-503, Straight Permucosal Ext, 5mm x 3mm
Brand
BioHorizons Implant Systems Inc One Perimeter Park South
Lot Codes / Batch Numbers
Lot No. C0205048
Products Sold
Lot No. C0205048
BioHorizons Implant Systems Inc One Perimeter Park South is recalling The Maestro System 204-503, Straight Permucosal Ext, 5mm x 3mm due to The product labeled as a Straight Permucosal Ext, 5mm x 3mm contained a profile abutment for Cement.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The product labeled as a Straight Permucosal Ext, 5mm x 3mm contained a profile abutment for Cement.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
MI, PA, TX, VA
Page updated: Jan 10, 2026