Recall Z-0298-2018
Zimmer Biomet, Inc. · initiated June 5, 2017
Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature
Product
COMP 12MM HUM FRAC STEM MACRO, model # 11-113562
Codes / lots: Lot Number: 529890
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-0298-2018
- Initiated
- June 5, 2017
- Terminated
- March 6, 2018
- Product code
- KWT – Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented
- Distribution
- Nationwide in US; Internationally Argentina, Netherlands & Canada
- Recalling firm
- Zimmer Biomet, Inc., Warsaw, IN
Other products in the same recall event
| Recall | Product | Initiated |
|---|---|---|
| Z-0296-2018 Class II | Lateral 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 II | Lateral 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-0299-2018 Class II | COMP 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 II | ECHO 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-0301-2018 Class II | CER OPTION TYPE 1 TPR SLEVE -6, model # 650-1064Possibility that the patient label inside the product box was incorrectly labeled. The outer box label and… | 06/05/2017Terminated |
| Z-0302-2018 Class II | CER 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 II | OSS 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 II | RED 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 II | RED 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 |