Zimmer Inc. Quicklock Tracker, Size 2, Manufactured by Orthosoft, Montreal, Canada; Distributed by Smith & Nephew, Inc., Memphis, TN; ref: 111.100. Device is a surgical instrument. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Quicklock Tracker, Size 2, Manufactured by Orthosoft, Montreal, Canada; Distributed by Smith & Nephew, Inc., Memphis, TN; ref: 111.100. Device is a surgical instrument.
Brand
Zimmer Inc.
Lot Codes / Batch Numbers
Lots: PC040050, PC030403, PC040292, PC040293, PC050034, PC050129 and PC050034-1.
Products Sold
Lots: PC040050, PC030403, PC040292, PC040293, PC050034, PC050129 and PC050034-1.
Zimmer Inc. is recalling Quicklock Tracker, Size 2, Manufactured by Orthosoft, Montreal, Canada; Distributed by Smith & Nephe due to The three-point array may break during use, resulting in surgical delay and an increased risk of infection.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The three-point array may break during use, resulting in surgical delay and an increased risk of infection.
Recommended Action
Per FDA guidance
Consignee was notified by phone and email on or about 4/27/06. Contact Zimmer Inc. at 1-574-267-6131 for assistance.
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