Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Class 2 Device Recall Accolade TMZF Plus Femoral Stem

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back to Search Results
 Class 2 Device Recall Accolade TMZF Plus Femoral Stemsee related information
Date Initiated by FirmOctober 23, 2012
Date PostedJanuary 08, 2013
Recall Status1 Terminated 3 on September 11, 2013
Recall NumberZ-0656-2013
Recall Event ID 61718
510(K)NumberK994366 
Product Classification Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate - Product Code MEH
ProductAccolade TMZF Plus 127 degree Neck Angle V40 Hip Stem #2.5 and Accolade TMZF Plus 127 degree Neck Angle V40 Hip Stem #3.5, Howmedica Osteonics Corp. The intended use is for reconstruction of the head and neck of the femoral joint.
Code Information Catalog Number: 6021-2530 Lot #40264005  Catalog Number: 6021-3535 Lot #40163005. This lot was not received in the US.
Recalling Firm/
Manufacturer		 Stryker Howmedica Osteonics Corp.
325 Corporate Drive
Mahwah NJ 07430
For Additional Information ContactMs. Colleen O'Meara
201-972-2100
Manufacturer Reason
for Recall		Stryker has received a report that single size 3.5 stem was packaged as size 2.5 stem resulting in a possible product mix.
FDA Determined
Cause 2		Labeling mix-ups
ActionStryker sent "Urgent Medical Device Recall Notification" letters and product accountability forms via Fed Ex with return receipt on 10/23/12 to branches/agencies and to hospitals and physicians on 10/24/12. The letter described the issue and provided recommended actions to mitigate the risk. Customers can call (201) 972-2100 if questions.
Quantity in Commerce6021-2530- four units; 6021-3535-
DistributionNationwide distribution, including the states of NY, NJ, CA and FL.
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.
510(K) Database510(K)s with Product Code = MEH
-
-