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U.S. Department of Health and Human Services

Class 2 Device Recall Hipstar V40 Femoral Stem

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 Class 2 Device Recall Hipstar V40 Femoral Stemsee related information
Date Initiated by FirmSeptember 28, 2007
Date PostedDecember 14, 2007
Recall Status1 Terminated 3 on October 27, 2008
Recall NumberZ-0467-2008
Recall Event ID 45334
Product Classification Femoral Stem - Product Code LPH
ProductHipstar V40 Femoral Stem-127 degrees; N degrees 3 high offset 31 mm;Catalog No: 7850-5-005, IMPLANT SIZE 5, Sterile; Howmedica,Benoist Girard dt Cie, 203 bd de la Grande Della B.P.8;14291 Herouville Saint Clair
Code Information Lot Number:  G1312701, G1479782, G1479783, G1540972, G1560387, G1576137, G1576139, G1615995, G1615996, G1618366, and  G1618367 
Recalling Firm/
Manufacturer
Stryker Howmedica Osteonics Corp.
325 Corporate Dr
Mahwah NJ 07430-2002
For Additional Information Contact
201-831-5000
Manufacturer Reason
for Recall
Mis-labeling; The warning label "Do not use with heads more than +10mm offset" does not appear on 127 degree stem boxes.
FDA Determined
Cause 2
Packaging process control
ActionUrgent Product Correction/Recall notification letters were sent by Fed Ex return receipt on 9/28/07, requesting quarantine for Styker representatives to return or re-label.
Quantity in Commerce123
DistributionNationwide- USA including states of OR, AZ, NV, MI, AL, MI, FL, MN, and CA
Total Product Life CycleTPLC Device Report

1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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