| Date Initiated by Firm | April 19, 2017 |
| Create Date | July 28, 2017 |
| Recall Status1 |
Terminated 3 on March 19, 2019 |
| Recall Number | Z-2780-2017 |
| Recall Event ID |
77490 |
| 510(K)Number | K121575 |
| Product Classification |
Rod, fixation, intramedullary and accessories - Product Code HSB
|
| Product | Oxford/Oxbridge AFN End Cap
10 mm x 5 mm tp 12 mm x10 mm
The end caps are a circular disk with a small threaded shaft to be screwed to the distal end of the Nail. |
| Code Information |
Item Code OS331107 S1009023 Mar-2017 S1009023 Mar-2017 Item Code OS331104 S1009020 Apr-2017 Item Code OS331100 995035 Aug-2017; Jan-2018 Item Code OS331100 S1212114 May-2018 Item Code OS331101 S1009017 Jun-2018 Item Code OS331103 S1009019 Oct-2018 Item Code OS331105 S1102004 Oct-2018 Item Code OS331100 S1307176 Nov-2018, Dec-2018 S1401116 Apr-2019 Item Code OS331103 S1009019 May-2019 Item Code OS331105 S1102004 May-2019 Item Code OOS331100 7802 Oct-2019 |
| FEI Number |
3022270316
|
Recalling Firm/ Manufacturer |
Ortho Solutions Inc 330 Franklin Tpke Mahwah NJ 07430-3524
|
Manufacturer Reason for Recall | There is a material mislabeling of the AFN End Cap. |
FDA Determined Cause 2 | Error in labeling |
| Action | Orthosol notified their customers on 4/19/2017 via USPS. |
| Quantity in Commerce | 277 units |
| Distribution | US distribution to MD, NY & PA |
| 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 = HSB
|