Biomet 3 i, Disposable Twist Drills, Model Number DT2715. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Biomet 3 i, Disposable Twist Drills, Model Number DT2715.
Lot Codes / Batch Numbers
Lot Numbers: 635699 and 652460
Products Sold
Lot Numbers: 635699 and 652460
A medical device manufacturer is recalling Biomet 3 i, Disposable Twist Drills, Model Number DT2715. due to The depth indicator laser line markings on the drills are too faint for clinicians to read during use.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The depth indicator laser line markings on the drills are too faint for clinicians to read during use.
Recommended Action
Per FDA guidance
Each domestic consignee was contacted on 5/14/07 by phone using a prepared script. A follow up letter was then faxed to each consignee. International consignees were contacted by email followed by a faxed letter. Each consignee was instructed to examine their inventory for the recalled product. They were requested to complete and fax back a response form to Biomet and to return any affected product.
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
CA, DE, FL, IL, KS, MD, MA, MI, NJ, NY, RI, VA
Page updated: Jan 10, 2026