Implant Innovations, Inc. Products are surgical drills packaged separately or included in a surgical kit so two products will be listed. The second product is the 8mm drill included in a kit and It is labeled as OFKIT2 OsseoFix System Complete (Kit)3i Implant Innovations, Inc. 4555 Riverside drive, Palm Beach Gardens, FL 33410 Non Sterile Contents must be sterilized prior to use. RX only. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Products are surgical drills packaged separately or included in a surgical kit so two products will be listed. The second product is the 8mm drill included in a kit and It is labeled as OFKIT2 OsseoFix System Complete (Kit)3i Implant Innovations, Inc. 4555 Riverside drive, Palm Beach Gardens, FL 33410 Non Sterile Contents must be sterilized prior to use. RX only.
Brand
Implant Innovations, Inc.
Lot Codes / Batch Numbers
lot numbers 127726 and 191427
Products Sold
lot numbers 127726 and 191427
Implant Innovations, Inc. is recalling Products are surgical drills packaged separately or included in a surgical kit so two products will due to Some 8mm OsseoFix drills may be incorrectly laser marked as 4mm OsseoFix drills.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Some 8mm OsseoFix drills may be incorrectly laser marked as 4mm OsseoFix drills.
Recommended Action
Per FDA guidance
The firm faxed and e-mailed a recall communication to international accounts on 5/9/2003 and mailed recall letters to domestic accounts on 5/12/2003. The firms were requested to examine their stock and return product as well as to notify any subaccounts of the recall and recover and return their products. Letters to specific consignees only listed the recalled lot numbers that were shipped to that consignee. A response form was included and was to be faxed back to the recalling firm.
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 noticePage updated: Jan 10, 2026