FDA Device recall Z-1795-2020
CareFusion Safe-T-Centesis Catheter Drainage Tray, Sterile, For Single Use Only, Rx only, Catalog Number PIG1280T, UDI Number 01)1088540310…
- FDA Device
- Class II
- terminated
- Published 2020-05-06
On 2020-05-06 the FDA classified a Class II recall of CareFusion Safe-T-Centesis Catheter Drainage Tray, Sterile, For Single Use Only, Rx only, Catalog Number PIG1280T, UDI Number 01)1088540310… by Becton Dickinson And, citing the 8 Fr catheter was manufactured with the 6.9 Fr needle instead of the 8 Fr needle.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1795-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-03-26 |
| Published | 2020-05-06 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Becton Dickinson And |
| Distribution | AL, CO, IL, MA, MO, OK, RI, VA, WI |
Product
CareFusion Safe-T-Centesis Catheter Drainage Tray, Sterile, For Single Use Only, Rx only, Catalog Number PIG1280T, UDI Number 01)10885403108402(17) 210930(10)0001304986
Reason
The 8 Fr catheter was manufactured with the 6.9 Fr needle instead of the 8 Fr needle.
Identifiers
| code_info | Lot Number: 0001304986 |
|---|
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-1795-2020%22
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