FDA Device recall Z-1084-2018
ST. CHRISTOPHER'S SECUREMENT SET
- FDA Device
- Class II
- terminated
- Published 2018-03-28
On 2018-03-28 the FDA classified a Class II recall of ST. CHRISTOPHER'S SECUREMENT SET 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-1084-2018 |
| 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
ST. CHRISTOPHER'S SECUREMENT SET
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 | CSS685 Lot codes: 2015080390 2015092890 2015113090 2016011890 2016031490 2016042590 2016061390 2016071190 2…CSS685 Lot codes: 2015080390 2015092890 2015113090 2016011890 2016031490 2016042590 2016061390 2016071190 2016082290 2016092690 2016110790 2017011690 2017021390 2017031390 2017032790 2017081890 |
|---|
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-1084-2018%22
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