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U.S. Department of Health and Human Services

Class 2 Device Recall Specialist 2

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 Class 2 Device Recall Specialist 2see related information
Date Initiated by FirmFebruary 05, 2013
Date PostedMarch 19, 2013
Recall Status1 Terminated 3 on January 06, 2014
Recall NumberZ-0971-2013
Recall Event ID 63973
Product Classification Orthopedic manual surgical instrument - Product Code LXH
ProductSpecialist 2 IM Rod, Non-Sterile and associated Surgical Techniques: Sigma HP Instruments Classic Surgical Technique,0612-89-510 Sigma HP Instruments Balanced Surgical Technique, 0612-88-510 Sigma HP Instruments Fixed Reference Surgical Technique, 0612-87-510 PFC Sigma Knee Systems Primary Cruciate-Retaining & Cruciate-Substituting Procedure Surgical Technique,SP2-007 Product Usage: The SP2 IM Rod is used in both primary and revision Sigma knee procedures to align the femoral locating device and distal femoral cutting block. It is also used with the IM tibial resection. This rod is included in both the SP2 and HP instrument kits.
Code Information Product Code 96-6120 Label code / Etch code C3JHN4 H0808 C3JHS4 H0908 C3JHF4 H1008 C4GA54  C4GCC4  C4GBT4  C52F74 H1108 C52GV4 H1208 C52GL4  C67N14  C98CS4 H0109 C98BF4  DE5P34 H0309 DE5RP4  DF4H44  DG9LK4 H0409 DG9L64  DJ5E34  DK3E34 H0509 DK3FE4  EB5FV4 H0210 D95AN4  EB5GH4 H0310 EC9JY4  EF4DJ4  EJ7AP4 H0410 ES2G64 H0510 EJ7A34  ES2HA4 H0610 ES2HY4 H0710 EX5L44  EX5MS4 H0810 E2SD44 H0910 FA4G94 H0211 FD8MP4 H0311 FH8JA4  FH8JX4 H0611 TBACC TBACC TBACZ TBACZ FJ4E74 TBAGG 
Recalling Firm/
Manufacturer		 DePuy Orthopaedics, Inc.
700 Orthopaedic Dr
Warsaw IN 46582-3994
For Additional Information ContactMindy Tinsley
574-372-7136
Manufacturer Reason
for Recall		Potential for the IM rod to break, leaving fragments in the patient. Surgical Techniques guidance has been updated until design changes can be made to reduce likelihood of potential failure.
FDA Determined
Cause 2		Device Design
ActionDePuy Orthopaedics sent an Urgent Medical Device Correction Notice letter dated February 5, 2013 to all affected customers. The letter identified the affected product, problem and actions to be taken. Customers were asked to complete and return the FAX back form to FAX 574-371-4939 or email kseppa@its.jnj.com Questions about device correction information call Post Market Surveillance, 574-372-7333, Sales force questions call Product Specialist, 574-372-7303 and Surgeon questions DePuy's Scientific Information Office at 1-888-554-2482.
Quantity in Commerce4000; 2600 in USA
DistributionWorldwide Distribution - USA Nationwide.
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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