| Date Initiated by Firm |
October 23, 2017 |
| Create Date |
March 17, 2018 |
| Recall Status1 |
Terminated 3 on June 21, 2018 |
| Recall Number |
Z-1082-2018 |
| Recall Event ID |
79329 |
| Product Classification |
Tray, surgical - Product Code LRP
|
| Product |
CIRCUMCISION TRAY |
| Code Information |
CIT6020 CIT6120 Lot codes: 2015081790 2015112090 2016011190 2016022390 2016031690 2016042690 2016061590 2016080890 2016090690 2016100790 2017010990 2017020990 2017040490 2017051590 2017061690 2015111390 2016012190 2016022390 2016033190 2016060690 2016071890 2016092290 2016111590 2017020990 2017030790 2017041390 2017051590 |
Recalling Firm/
Manufacturer |
Centurion Medical Products Corporation
100 Centurion Way
Williamston MI 48895-9086
|
Manufacturer Reason
for Recall |
Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
|
FDA Determined
Cause 2 |
Nonconforming Material/Component |
| Action |
On October 16, 2017 a PRODUCT CORRECTION letter was issued to customers notifying them that if they had any kits in their inventory, Centurion will supply labels to affix to the front of each kit instructing the user to discard the prep pad upon opening the kit. Other components of the kit may continue to be used and are NOT within the scope of this recall. |
| Distribution |
Nationally |
| 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.
|
