FDA Device recall Z-1096-2018
EXCISION TRAY
- FDA Device
- Class II
- terminated
- Published 2018-03-28
On 2018-03-28 the FDA classified a Class II recall of EXCISION TRAY by Centurion Medical Products, citing convenience Kit containing components to assist practitioner with IV placement and securement.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1096-2018 |
| 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
EXCISION TRAY
Reason
Convenience Kit containing components to assist practitioner with IV placement and securement.
Identifiers
| code_info | MNS2790 Lot codes: 2016010490 2016033190 2016082990 2016120590 2017042090 2017090490 |
|---|
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-1096-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.