Wright Medical Technology Inc Odyssey Femoral Holder/Driver, Part Number K001-7410, Non-sterile, 1 each, Wright Medical Technology, Inc., 5677 Airline Road, Arlington, TN 38002 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Odyssey Femoral Holder/Driver, Part Number K001-7410, Non-sterile, 1 each, Wright Medical Technology, Inc., 5677 Airline Road, Arlington, TN 38002
Brand
Wright Medical Technology Inc
Lot Codes / Batch Numbers
Lot Numbers: 047367193, 067380510, and 077414021
Products Sold
Lot Numbers: 047367193, 067380510, and 077414021
Wright Medical Technology Inc is recalling Odyssey Femoral Holder/Driver, Part Number K001-7410, Non-sterile, 1 each, Wright Medical Technology due to Breakage: breaking of the connecting foot that is on the distal surface of the instrument. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Breakage: breaking of the connecting foot that is on the distal surface of the instrument
Recommended Action
Per FDA guidance
The firm notified their distributors of the recall on October 4, 2007, with an Urgent Medical Device Recall letter explaining the problem and requesting return of the product from their inventory and from their consignees. The hospitals were notified of the recall on October 4, 2007 using the same Urgent Device Recall Letter.
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