Stryker Howmedica Osteonics Corp. Howmedica Osteonics Corp. Restoration Modular Revision Hip System, Plasma Distal Stem; Titanium, Alloy and Hydroxyapatite. Catalog number: 6276-5-014. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Howmedica Osteonics Corp. Restoration Modular Revision Hip System, Plasma Distal Stem; Titanium, Alloy and Hydroxyapatite. Catalog number: 6276-5-014.
Brand
Stryker Howmedica Osteonics Corp.
Lot Codes / Batch Numbers
Catalog number: 6276-5-014, Lot number: 20568201, Exp 11/23/2011.
Products Sold
Catalog number: 6276-5-014; Lot number: 20568201, Exp 11/23/2011.
Stryker Howmedica Osteonics Corp. is recalling Howmedica Osteonics Corp. Restoration Modular Revision Hip System, Plasma Distal Stem; Titanium, All due to The Restoration Modular Hip Stem may have two different package labels. The 14 mm diameter stem may be labeled with both a size 14 mm diameter and a 2. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The Restoration Modular Hip Stem may have two different package labels. The 14 mm diameter stem may be labeled with both a size 14 mm diameter and a 26 mm diameter.
Recommended Action
Per FDA guidance
Stryker Branches were notified by e-mail on December 30, 2009. This was followed by a formal recall letter by Fed Ex sent on 1/11/10 to branches as well as the hospital and surgeon that used the device.
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
GA, IN
Page updated: Jan 10, 2026