FDA Device recall Z-1093-2018
IV START KIT
- FDA Device
- Class II
- terminated
- Published 2018-03-28
On 2018-03-28 the FDA classified a Class II recall of IV START KIT 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-1093-2018 |
| 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
IV START KIT
Reason
Convenience Kit containing components to assist practitioner with IV placement and securement.
Identifiers
| code_info | IV6860 IVS1345 Lot codes: 2015110290 2016011190 2016030790 2016050290 2016061390 2016081590 2016101090 2017…IV6860 IVS1345 Lot codes: 2015110290 2016011190 2016030790 2016050290 2016061390 2016081590 2016101090 2017010290 2017021390 2017032090 2017050890 2017071790 2015110990 2016020890 2016062090 2016071190 2016072590 2016080890 2016082990 2016090590 2016091990 |
|---|
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-1093-2018%22
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