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

  • 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 see related information
Date Initiated by Firm April 17, 2020
Create Date May 28, 2020
Recall Status1 Terminated 3 on June 25, 2021
Recall Number Z-2152-2020
Recall Event ID 85524
510(K)Number K060525  
Product Classification Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer - Product Code JWH
Product Knee Products:
189420 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 63 MM
189422 Vanguard Knee System, PS Mono Lock Tibial Bearing, 12 MM X 63 MM
189442 Vanguard Knee System, PS Mono Lock Tibial Bearing, 12 MM X 67 MM
189460 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 71 MM
189440 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 67 MM
189460 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 71 MM
189420 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 63 MM
189460 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 71 MM
189426 Vanguard Knee System, PS Mono Lock Tibial Bearing, 16 MM X 63 MM
189440 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 67 MM
189460 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 71 MM
Code Information Lot Numbers: UDI Number 530900 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 63 MM (01)00880304451735(17)211223(10)530900 548950 Vanguard Knee System, PS Mono Lock Tibial Bearing, 12 MM X 63 MM (01)00880304451360(17)211222(10)548950 602870 Vanguard Knee System, PS Mono Lock Tibial Bearing, 12 MM X 63 MM (01)00880304451360(17)211228(10)602870 530930 Vanguard Knee System, PS Mono Lock Tibial Bearing, 12 MM X 67 MM (01)00880304451346(17)211223(10)530930 588890 Vanguard Knee System, PS Mono Lock Tibial Bearing, 12 MM X 67 MM (01)00880304451346(17)211223(10)588890 602930 Vanguard Knee System, PS Mono Lock Tibial Bearing, 12 MM X 67 MM (01)00880304451346(17)211228(10)602930 697510 Vanguard Knee System, PS Mono Lock Tibial Bearing, 12 MM X 67 MM (01)00880304451346(17)211227(10)697510 700830 Vanguard Knee System, PS Mono Lock Tibial Bearing, 12 MM X 67 MM (01)00880304451346(17)211228(10)700830 530940 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 71 MM (01)00880304451322(17)211223(10)530940 758560 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 71 MM (01)00880304451322(17)211228(10)758560 758580 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 71 MM (01)00880304451322(17)211223(10)758580 884710 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 67 MM (01)00880304451308(17)211229(10)884710 570620 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 67 MM (01)00880304451308(17)220106(10)570620 884680 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 67 MM (01)00880304451308(17)220107(10)884680 828010 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 71 MM (01)00880304451322(17)220106(10)828010 855380 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 71 MM (01)00880304451322(17)220111(10)855380 855390 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 71 MM (01)00880304451322(17)220111(10)855390 772740 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 63 MM (01)00880304451735(17)220112(10)772740 796110 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 63 MM (01)00880304451735(17)220115(10)796110 796120 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 63 MM (01)00880304451735(17)220112(10)796120 796150 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 71 MM (01)00880304451322(17)220112(10)796150 828040 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 71 MM (01)00880304451322(17)220115(10)828040 830730 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 71 MM (01)00880304451322(17)220115(10)830730 727060 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 63 MM (01)00880304451735(17)220121(10)727060 505430 Vanguard Knee System, PS Mono Lock Tibial Bearing, 16 MM X 63 MM (01)00880304454859(17)220125(10)505430 581950 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 67 MM (01)00880304451308(17)220121(10)581950 608380 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 67 MM (01)00880304451308(17)220118(10)608380 644080 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 67 MM (01)00880304451308(17)220118(10)644080 708620 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 67 MM (01)00880304451308(17)220121(10)708620 758570 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 71 MM (01)00880304451322(17)220118(10)758570 
Recalling Firm/
Manufacturer		 Biomet, Inc.
56 E Bell Dr
Warsaw IN 46582-6989
For Additional Information Contact 411 Technical Services
574-371-3071
Manufacturer Reason
for Recall		 Potential presence of elevated endotoxin levels that exceed the specification limit
FDA Determined
Cause 2		 Process control
Action Zimmer Biomet issued Urgent Medical Device recall letter dated April 17, 2002 to distributors with direct sales and/or field inventory via email and traceable letter sent via FedEx. Hospitals with direct sales or current inventory, as well as hospitals that have consumed products will be notified via FedEx. Surgeons that have consumed products will be notified via FedEx. Action to take: 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. This form must be returned even if you do not have affected products available to return in your territory. b. For international returns, request an IRA by emailing zimmerbiometintlirarequests@zimmerbiomet.com c. For each return, send a copy of Attachment 1 to CorporateQuality.PostMarket@zimmerbiomet.com. CF04107 Rev. 4, Eff. Date: 16 Jul 2019 Ref. CP04102 Field Action Activities d. Include a hardcopy of Attachment 1 in each carton of your return shipment for immediate processing. e. Mark RECALL on the outside of the returned cartons. 4. Return the Additional Accounts form to CorporateQuality.PostMarket@zimmerbiomet.com. a. Review the list of hospitals and/or surgeons included with the email notification sent to your facility, which includes a list of hospitals and/or surgeons that have already been notified of this recall. b. Identify whether there are any additional hospitals and/or surgeons that Zimmer Biomet has not notified and list these accounts on the Additional Accounts form. Please provide the form in Excel format. c. If there are no additional accounts or surgeons to notify, please indicate that there are no additional accounts, or i
Quantity in Commerce 107 units
Distribution Worldwide distribution - US Nationwide distribution and the countries of Canada, AHMADABAD, GUJARAT, BANGKOK, BELROSE NSW, BUENOS AIRES, CHILE, COSTA RICA, HIRATSUKA CITY, HUECHURABA SANTIAGO, INDIA, JAPAN, MEXICO DF, NETHERLANDS, PICHINCHA, EC, SAN JOSE, SINGAPORE, TAIWAN, THAILAND, YONGSAN-GU SEOUL.
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 = BIOMET MANUFACTURING CORP.
-
-