Medical Devices
HA Hip Stem, cementless Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
HA Hip Stem, cementless
Lot Codes / Batch Numbers
Part number 470-02-090, Lot 938381
Products Sold
Part number 470-02-090, Lot 938381
A medical device manufacturer is recalling HA Hip Stem, cementless due to Hip stem product was mis-labeled with wrong size.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Hip stem product was mis-labeled with wrong size.
Recommended Action
Per FDA guidance
Firm sent letter of notification to consignee on 6/30/2004.
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
FL
Page updated: Jan 10, 2026