FDA Device recall Z-1082-2018
CIRCUMCISION TRAY
- FDA Device
- Class II
- terminated
- Published 2018-03-28
On 2018-03-28 the FDA classified a Class II recall of CIRCUMCISION TRAY by Centurion Medical Products, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1082-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-10-23 |
| Published | 2018-03-28 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Centurion Medical Products |
| Distribution | n/a |
Product
CIRCUMCISION TRAY
Reason
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.
Identifiers
| code_info | CIT6020 CIT6120 Lot codes: 2015081790 2015112090 2016011190 2016022390 2016031690 2016042690 2016061590 201…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 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1082-2018%22
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