Product is labeled as LTX XP Miniplant, Dental Implant, Sterile. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Product is labeled as LTX XP Miniplant, Dental Implant, Sterile.
Lot Codes / Batch Numbers
Model No. LTX3211 - Packaged Lot No. 606199 Model No. LTX3213 - Packaged Lot No. 606191
Products Sold
Model No. LTX3211 - Packaged Lot No. 606199 Model No. LTX3213 - Packaged Lot No. 606191
A medical device manufacturer is recalling Product is labeled as LTX XP Miniplant, Dental Implant, Sterile. due to The LTX XP Miniplant, BIOMET 3i dental implant, was labeled incorrectly. The 13MM implants were labeled and packaged as 11.5MM implants and 11.5MM im. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The LTX XP Miniplant, BIOMET 3i dental implant, was labeled incorrectly. The 13MM implants were labeled and packaged as 11.5MM implants and 11.5MM implants were labeled and packaged as 13MM implants.
Recommended Action
Per FDA guidance
International customers were contacted first by e-mail , then by fax letter 08/03/2007.
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