Zimmer Inc. Zimmer Durom Hip Resurfacing Systems, Femoral Component 54 Code T; Catalog No.: 01.00211.154, Zimmer, Warsaw, IN, 46581-0708. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Zimmer Durom Hip Resurfacing Systems, Femoral Component 54 Code T; Catalog No.: 01.00211.154, Zimmer, Warsaw, IN, 46581-0708.
Brand
Zimmer Inc.
Lot Codes / Batch Numbers
Lot 2376766.
Products Sold
Lot 2376766.
Zimmer Inc. is recalling Zimmer Durom Hip Resurfacing Systems, Femoral Component 54 Code T; Catalog No.: 01.00211.154, Zimmer due to Mislabeled as to size; 54mm package contains 46 mm device and vice versa.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Mislabeled as to size; 54mm package contains 46 mm device and vice versa.
Recommended Action
Per FDA guidance
Zimmer GmbH notified Distributors via a Product Recall Notification letter, dated 9/26/07, instructing them to return the products and to subrecall.
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