Zimmer Austin, Inc MOST Options System Porous and Non-Porous Revision Stem Adapters, manufactured and distributed by Zimmer Austin, Inc., Austin, Texas 78717 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
MOST Options System Porous and Non-Porous Revision Stem Adapters, manufactured and distributed by Zimmer Austin, Inc., Austin, Texas 78717
Brand
Zimmer Austin, Inc
Lot Codes / Batch Numbers
Catalog Numbers: 5000-50-100 and 5000-50-200, Lot Numbers: 1529444, 1536181, 1538936, 1538937, 1542189, 1568350, 1568351, 1569597, 1596886, 1596890, 1601839, 1601841, 1610470, 1616609, and 1617691
Products Sold
Catalog Numbers: 5000-50-100 and 5000-50-200; Lot Numbers: 1529444, 1536181, 1538936, 1538937, 1542189, 1568350, 1568351, 1569597, 1596886, 1596890, 1601839, 1601841, 1610470, 1616609, and 1617691
Zimmer Austin, Inc is recalling MOST Options System Porous and Non-Porous Revision Stem Adapters, manufactured and distributed by Zi due to Risk of adapter disassociation from mating components when assembled improperly or when subjected to high-stress femoral applications.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Risk of adapter disassociation from mating components when assembled improperly or when subjected to high-stress femoral applications.
Recommended Action
Per FDA guidance
The firm initiated the recall via letter on December 17, 2004. The firm''s letter requests the return of all recalled product.
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 noticeDistribution
As reported by FDA
AZ, CA, FL, IL, IN, MD, MI, MO, NY, OH, TX, WI
Page updated: Jan 10, 2026