FDA Device recall Z-1084-2020
Centurion IVS3505 ULTRASOUND GUIDED PIV KIT
- FDA Device
- Class II
- terminated
- Published 2020-02-12
On 2020-02-12 the FDA classified a Class II recall of Centurion IVS3505 ULTRASOUND GUIDED PIV KIT by Centurion Medical Products, citing incomplete seals on the sterile package may compromise the sterility.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1084-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-12-11 |
| Published | 2020-02-12 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Centurion Medical Products |
| Distribution | US |
Product
Centurion IVS3505 ULTRASOUND GUIDED PIV KIT
Reason
Incomplete seals on the sterile package may compromise the sterility
Identifiers
| code_info | Lot Code: 2019012390 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1084-2020%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.