FDA Device recall Z-0254-2020
Maintenance Flush Kit/Blood Draw Product Code: DT19335
- FDA Device
- Class II
- terminated
- Published 2019-11-06
On 2019-11-06 the FDA classified a Class II recall of Maintenance Flush Kit/Blood Draw Product Code: DT19335 by Centurion Medical Products, citing supplier initiated recall of the GRIPPER Needles.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0254-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-07-15 |
| Published | 2019-11-06 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Centurion Medical Products |
| Distribution | IL |
Product
Maintenance Flush Kit/Blood Draw Product Code: DT19335
Reason
Supplier initiated recall of the GRIPPER Needles
Identifiers
| code_info | Lot Number Expiration 2018110501 7/31/2021 2018121801 7/31/2021 2019013001 9/30/2021 2019032901 9/30/2021 |
|---|
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-0254-2020%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.