FDA Device recall Z-0161-2016
Nipro Safe Touch TULIP Safety Fistula Needle, FT+152530TP, for use as a blood access device for blood purification and for other treatments…
- FDA Device
- Class II
- terminated
- Published 2015-11-04
On 2015-11-04 the FDA classified a Class II recall of Nipro Safe Touch TULIP Safety Fistula Needle, FT+152530TP, for use as a blood access device for blood purification and for other treatments… by Nipro Medical, citing some 1 1/4" needles were packaged and labeled in the 1" blister package.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0161-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-08-13 |
| Published | 2015-11-04 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Nipro Medical |
| Distribution | IN |
Product
Nipro Safe Touch TULIP Safety Fistula Needle, FT+152530TP, for use as a blood access device for blood purification and for other treatments requiring an extracorporeal circuit of larger volumes of blood.
Reason
Some 1 1/4" needles were packaged and labeled in the 1" blister package.
Identifiers
| code_info | Lot # 15C03 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0161-2016%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.