Zimmer Inc. Zimmer ITST Intertrochanteric/subtrochanteric fixation tapered reamer, nonsterile; REF 2258-50-00. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Zimmer ITST Intertrochanteric/subtrochanteric fixation tapered reamer, nonsterile; REF 2258-50-00.
Brand
Zimmer Inc.
Lot Codes / Batch Numbers
Lots 60633223 and 60740476.
Products Sold
Lots 60633223 and 60740476.
Zimmer Inc. is recalling Zimmer ITST Intertrochanteric/subtrochanteric fixation tapered reamer, nonsterile; REF 2258-50-00. due to Reamers labeled as having a standard diameter may actually be the dimensions of an Asia reamer, and vice versa.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Reamers labeled as having a standard diameter may actually be the dimensions of an Asia reamer, and vice versa.
Recommended Action
Per FDA guidance
Zimmer sent an Urgent Device Recall letter dated 6/5/09 to all consignees and instructed to locate and return the products.
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