Stryker Howmedica Osteonics Corp. V 40 Femoral Head, Sterile, 22 mm; Catalog number 6260-4-122, Catalog number 6260-5-226; Howmedica Osteonics Corp., Stryker Ireland, Carrigtwohill County Cork, Ireland; Intended for use with femoral stems and acetabular components in primary or revision total hip arthroplasty. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
V 40 Femoral Head, Sterile, 22 mm; Catalog number 6260-4-122, Catalog number 6260-5-226; Howmedica Osteonics Corp., Stryker Ireland, Carrigtwohill County Cork, Ireland; Intended for use with femoral stems and acetabular components in primary or revision total hip arthroplasty.
Brand
Stryker Howmedica Osteonics Corp.
Lot Codes / Batch Numbers
lot # 29213701, Exp. 1/28/2014 and lot # 29228301, Exp 1/28/2014
Products Sold
lot # 29213701;Exp. 1/28/2014 and lot # 29228301; Exp 1/28/2014
Stryker Howmedica Osteonics Corp. is recalling V 40 Femoral Head, Sterile, 22 mm; Catalog number 6260-4-122, Catalog number 6260-5-226; Howmedica O due to Sterilization issue: During post-sterilization inspection of the outer blister packaging of the affected lots, it was determined that the outer bliste. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Sterilization issue: During post-sterilization inspection of the outer blister packaging of the affected lots, it was determined that the outer blister did not meet the required minimum seal width.
Recommended Action
Per FDA guidance
Urgent Product Recall letters were sent via Federal Express on June 18, 2009 to all Stryker Branches/Agencies, hospital Risk Management, hospital Chief of Orthopaedics and surgeons who may have used the recalled products. The letters stated the issue, potential hazards, and the risk mitigation. Customers may contact Colleen O'Meara at 201-831-5970 with any questions.
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