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U.S. Department of Health and Human Services

Class 2 Device Recall Zimmer

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  Class 2 Device Recall Zimmer see related information
Date Initiated by Firm January 11, 2016
Date Posted March 12, 2016
Recall Status1 Terminated 3 on April 13, 2017
Recall Number Z-1168-2016
Recall Event ID 72900
510(K)Number K963109  
Product Classification Prosthesis, hip, semi-constrained, metal/polymer, cemented - Product Code JDI
Product Product 70 consists of all product under product code: JDI and same usage:
Item no:
785701000 VERSYS HERITAGE FEM STEM
785701100 VERSYS HERITAGE FEM STEM
785701200 VERSYS HERITAGE FEM STEM
785701300 VERSYS HERITAGE FEM STEM
785701320 VERSYS HERITAGE FEM STEM
785701400 VERSYS HERITAGE FEM STEM
785701420 VERSYS HERITAGE FEM STEM
785701500 VERSYS HERITAGE FEM STEM
785701520 VERSYS HERITAGE FEM STEM
785701600 VERSYS HERITAGE FEM STEM
785701700 VERSYS HERITAGE FEM STEM

For use in total or hemi hip arthroplasty
Code Information lot no.: 61661156 61966578 62225735 61873650 61962858 62137227 62137228 62240762 62340060 62340060N 61820823 61881193 61957419 61962855 62172047 62175238 62234460 62262787 62291935 62298291 62298292 62310454 62314656 62340058 62298291N 62310454N 62314656N 62340058N 61878467 61881194 61883397 61886939 61899754 61968010 62221008 62284504 62285272 62291937 62291937N 61822322 62032180 62260128 62304808 62340062 62358896 62304808N 62340062N 61813932 61820819 61980168 62205493 62240263 62240771 62240772 62240773 62240774 62282932 62291138 62291938 62296576 62299089 62340063 62296576N 62340063N 61866252 62257147 62303509 62340064 62340064N 61814493 61976178 62046502 62240775 62312492 61679898 61995953 61995956 61995957 61995958 61885901 62046499 62211984 370462 61980171 
Recalling Firm/
Manufacturer		 Zimmer Manufacturing B.V.
Turpeaux Industrial Park Rd 1 km 123.4
Mercedita PR 00715
For Additional Information Contact Consumer Relations Call Center
800-447-5633
Manufacturer Reason
for Recall		 As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
FDA Determined
Cause 2		 Packaging
Action Zimmer Biomet sent an Urgent Medical Device Recall Letter, dated January 11, 2016, to Distributors, Sales Representatives, Operation Managers, and Risk Managers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to 1.Review the notification and ensure that relevant personnel are aware of the contents. 2. Assist your Zimmer Biomet sales representative with the quarantine of any affected product. 3. Your Zimmer Biomet sales representative will remove the recalled product from your facility. 4. Complete and return the attached Certificate of Acknowledgment form to corporatequality.postmarket@zimmerbiomet.com. 5. If after reviewing this notification you have further questions or concerns please call Customer Service at 1-800-348-2759, or contact your Zimmer Biomet Sales Representative.
Quantity in Commerce 360
Distribution US Nationwide Distribution
Total Product Life Cycle TPLC 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) Database 510(K)s with Product Code = JDI and Original Applicant = ZIMMER, INC.
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