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U.S. Department of Health and Human Services

Class 2 Device Recall NATURALKNEE II SYSTEM

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  Class 2 Device Recall NATURALKNEE II SYSTEM see related information
Date Initiated by Firm November 29, 2017
Create Date March 14, 2018
Recall Status1 Terminated 3 on April 02, 2020
Recall Number Z-1033-2018
Recall Event ID 78706
510(K)Number K936159  
Product Classification Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer - Product Code JWH
Product NP FEM LT SZ0 NATURAL-KNE
NP FEM RT SZ0 NATURAL-KNE
NP FEM LT SZ2 NATURAL-KNE
NP FEM RT SZ2 NATURAL-KNE
NP FEM LT SZ3 NATURAL-KNE

The Natural-Knee II System with Cancellous-Structured Titanium (CSTi) Porous Coating
Code Information 6307-00-008 62125578 6307-00-020 61975784 6307-00-020 62098206 6307-00-030 11004845 6307-00-030 62142198 6307-00-009 62107229 6307-00-021 11004878 6307-00-021 62160819 6307-00-021 62155319 6307-00-021 62162357 6307-00-021 62164084 6307-00-021 62176798 6307-00-021 62174770 6307-00-021 62173770 6307-00-021 62177132 6307-00-021 62172373 6307-00-021 62178184 6307-00-021 62178731 6307-00-021 62183228 6307-00-021 62180483 6307-00-021 62185696 6307-00-021 62181538 6307-00-021 62188142 6307-00-021 11007719 6307-00-021 62189950 6307-00-021 62193587 6307-00-021 62190389 6307-00-021 62192798 6307-00-021 62196210 6307-00-021 62194526 6307-00-021 11007656 6307-00-021 62200791 6307-00-021 62203902 6307-00-021 62206609 6307-00-021 11007666 6307-00-021 62191204 6307-00-021 11007831 6307-00-021 11007677 6307-00-021 11007922 6307-00-021 11007925 6307-00-021 11007944 6307-00-021 62210574 6307-00-021 62208953 6307-00-021 62210107 6307-00-021 62207438 6307-00-021 11008018 
Recalling Firm/
Manufacturer		 Zimmer Biomet, Inc.
1800 W Center St
Warsaw IN 46580-2304
For Additional Information Contact Kevin W. Escapule
574-372-4487
Manufacturer Reason
for Recall		 The LDPE bag packaging for various highly polished hip and knee implants may adhere to the highly polished surface, leaving residue or material from the LDPE bag on the implant after it is removed from the bag.
FDA Determined
Cause 2		 Packaging
Action A similar recall was initiated in January 2016 to remove remaining inventory packaged in the old bag. Further evaluation identified additional lots packaged in the old bag that were not included in the January 2016 recall; therefore, resulting in this new recall for the additional lots packaged in the old bag. A firm, Zimmer Biomet, sent an "Urgent Medical Device Recall" notices dated November 29, 2017 and response forms to customers. The notice described the product, problem and actions to be taken. The Customers should take the following action: Risk Manager Responsibilities: 1. Review this notification and ensure that affected personnel are aware of the contents. 2. If you have affected product at your facility, assist your Zimmer Biomet sales representative and quarantine all affected product. Your Zimmer Biomet sales representative will remove the affected product from your facility. 3. Complete Attachment 1  Certificate of Acknowledgement and send to CorporateQuality.PostMarket@zimmerbiomet.com. This form must be returned even if you do not have affected products at your facility. 4. Retain a copy of the acknowledgement form with your recall records in the event of a compliance audit of your facilitys documentation. Distributor Responsibilities: 1. Review this notification and ensure that affected team members are aware of the contents. 2. Immediately locate and quarantine affected product in your inventory. 3. Immediately return all affected product from your distributorship and from affected hospitals within your territory. a. Complete Attachment 1  Inventory Return Certification Form and send to CorporateQuality.PostMarket@zimmerbiomet.com within three (3) days. b. For each return, send a copy of Attachment 1 to CorporateQuality.PostMarket@zimmerbiomet.com. c. Include a hardcopy of Attachment 1 in each carton of your return shipment for immediate processing. d. Mark RECALL on the outside of the returned cartons. 4. Return the Additi
Quantity in Commerce 13,227 in total
Distribution Worldwide Distribution: US (nationwide) and countries of: Argentina, Australia, Brazil, Bolivia, Canada, Chile, China, Colombia, Ecuador, El Salvador, India, Japan, Malaysia, Mexico, Netherlands, New Zealand, Nicaragua, Panama, Seoul-Korea, Singapore, Taiwan, Thailand, and UAE.
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 = JWH and Original Applicant = INTERMEDICS ORTHOPEDICS
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