Recall Z-0301-2018

Zimmer Biomet, Inc. · initiated June 5, 2017

Class II Terminated

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

CER OPTION TYPE 1 TPR SLEVE -6, model # 650-1064

Codes / lots: Lot Number: 854540

Reason for recall

Possibility that the patient label inside the product box was incorrectly labeled. The outer box label and actual product are correctly identified but the internal patient label could be incorrect.

FDA-determined cause: Labeling False and Misleading

Action taken

On June 5, 2017, Zimmer Biomet distributed Urgent Medical Device Recall notices to their customers via email and Fed Ex courier service. ***Risk Managers are advised to: 1. Review this notification and ensure affected personnel are aware of the contents. 2. Assist your Zimmer Biomet sales representative to quarantine all affected product. 3. Work with your Zimmer Biomet sales representative in removing the affected product from your facility. 4. Confirm that the patient labels in your records are correct. 5. Complete the Certificate of Acknowledgement and return a digital copy to corporatequality.postmarket@zimmerbiomet.com and retain a copy of the Acknowledgement Form with your recall records in the event of a compliance audit of your facilities documentation. ****Distributors, Sales Reps & Distributor Operation Managers are advised to: 1. Review this notification and ensure affected team members are aware of the contents. 2. Immediately locate and quarantine affected product in your inventory. 3. Complete the Certification of Acknowledgement portion of Attachment 1 Inventory Return Certification Form and return a digital copy to corporatequality.postmarket@zimmerbiomet.com within three (3) days. 4. Immediately return all affected product from your distributorship and affected hospitals within your territory along with a completed Attachment 1 Inventory Return Certification Form to Zimmer Biomet. a. Request a Recall Return Authorization Number via SMS or via email to rgarequest@zimmerbiomet.com (domestic) or via email to zimmerbiometintlirarequests@zimmerbiomet.com (international). b. For each return, send a copy of Attachment 1 to corporatequality.postmarket@zimmerbiomet.com. c. Include a hardcopy of Attachment 1 with your shipment for immediate processing. d. Mark the outside of the returns box(es) clearly with RECALL. Customers with further questions or concerns please call the customer call center at 1-574-371-3071 between 8:00 am and 5

Details

Recall number
Z-0301-2018
Initiated
June 5, 2017
Terminated
March 6, 2018
Product code
LZO – Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
Distribution
Nationwide in US; Internationally Argentina, Netherlands & Canada
Recalling firm
Zimmer Biomet, Inc., Warsaw, IN

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-0296-2018 Class IILateral Troch Plate Full Crimp - 254mm, model # 350837Possibility that the patient label inside the product box was incorrectly labeled. The outer box label and… 06/05/2017Terminated
Z-0297-2018 Class IILateral Troch Plate Full Crimp - 254mm, model # 350838Possibility that the patient label inside the product box was incorrectly labeled. The outer box label and… 06/05/2017Terminated
Z-0298-2018 Class IICOMP 12MM HUM FRAC STEM MACRO, model # 11-113562Possibility that the patient label inside the product box was incorrectly labeled. The outer box label and… 06/05/2017Terminated
Z-0299-2018 Class IICOMP PRIMARY STEM 8MM MINI, model # 113628Possibility that the patient label inside the product box was incorrectly labeled. The outer box label and… 06/05/2017Terminated
Z-0300-2018 Class IIECHO POR FMRL NC 9X125, model # 192009Possibility that the patient label inside the product box was incorrectly labeled. The outer box label and… 06/05/2017Terminated
Z-0302-2018 Class IICER BIOLOXD OPTION HD 32MM, model # 650-1056Possibility that the patient label inside the product box was incorrectly labeled. The outer box label and… 06/05/2017Terminated
Z-0303-2018 Class IIOSS CEMENTED IM STEM 12X150, model # 150366Possibility that the patient label inside the product box was incorrectly labeled. The outer box label and… 06/05/2017Terminated
Z-0304-2018 Class IIRED SEXP DSTL FEM 19CM RT ASSY, model # CP111817Possibility that the patient label inside the product box was incorrectly labeled. The outer box label and… 06/05/2017Terminated
Z-0305-2018 Class IIRED SEXP DSTL FEM 19CM LT ASSY, model # CP111828Possibility that the patient label inside the product box was incorrectly labeled. The outer box label and… 06/05/2017Terminated