Class 2 Device Recall NEXGEN POROUS, HA/TCP, UNCEMENTED FEMORAL AND TIBIAL BASEPLATE COMPONENTS

• Date Initiated by Firm: November 29, 2017
• Create Date: March 14, 2018
• Recall Status: Terminated on April 02, 2020
• Recall Number: Z-1031-2018
• Recall Event ID: 78706
• 510(K)Number: K041100
• Product Classification: Prosthesis, knee, patello/femorotibial, semi-constrained, uncemented, porous, coated, polymer/metal/polymer - Product Code MBH
• Product: CR-FLX POR HATCP FEM C-L MINUS; CR-FLX POR HATCP FEM C-R MINUS; CR-FLX POR HATCP FEM D-L MINUS; CR-FLX POR HATCP FEM D-R MINUS; CR-FLX POR HATCP FEM E-L MINUS; CR-FLX POR HATCP FEM E-R MINUS; CR-FLX POR HATCP FEM F-L MINUS; CR-FLX POR HATCP FEM F-R MINUS; CR-FLX POR HATCP FEM G-L MINUS; CR-FLX POR HATCP FEM G-R MINUS; ; This device is indicated for patients with severe knee pain and disability
• Code Information: 65-5952-013-05 61819644 65-5952-013-05 61855471 65-5952-013-05 11004433 65-5952-013-06 62056868 65-5952-014-05 61782591 65-5952-014-05 11003623 65-5952-014-05 61987912 65-5952-014-05 62104150 65-5952-014-06 61835232 65-5952-014-06 62038826 65-5952-014-06 62132128 65-5952-015-05 61782592 65-5952-015-05 61822359 65-5952-015-05 61857405 65-5952-015-05 11004436 65-5952-015-05 61939607 65-5952-015-05 62020177 65-5952-015-05 62046101 65-5952-015-05 62122758 65-5952-015-06 61805662 65-5952-015-06 11003505 65-5952-015-06 61848476 65-5952-015-06 11004261 65-5952-015-06 61921288 65-5952-015-06 61968654 65-5952-015-06 62001382 65-5952-015-06 62025672 65-5952-015-06 62074886 65-5952-015-06 62128161 65-5952-016-05 61801433 65-5952-016-05 61836563 65-5952-016-05 61857407 65-5952-016-05 11004258 65-5952-016-05 11004438 65-5952-016-05 61928636 65-5952-016-05 61951539 65-5952-016-05 62020178 65-5952-016-05 62056869 65-5952-016-05 62092424 65-5952-016-05 62139313 65-5952-016-06 61777547 65-5952-016-06 61822354 65-5952-016-06 61857408 65-5952-016-06 11004434 65-5952-016-06 61904112 65-5952-016-06 61939609 65-5952-016-06 62002454 65-5952-016-06 62020219 65-5952-016-06 62062056 65-5952-016-06 62104151 65-5952-017-05 61824510 65-5952-017-05 61893908 65-5952-017-05 61939612 65-5952-017-05 62005729 65-5952-017-05 62025675 65-5952-017-05 62086012 65-5952-017-05 62132131 65-5952-017-06 11003018 65-5952-017-06 61795937 65-5952-017-06 61822355 65-5952-017-06 11003671 65-5952-017-06 61861698 65-5952-017-06 61846121 65-5952-017-06 11004260 65-5952-017-06 61915980 65-5952-017-06 61987914 65-5952-017-06 62020182 65-5952-017-06 62038827 65-5952-017-06 62105368
• 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: 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 = MBH and Original Applicant = ZIMMER, INC.