FDA Device recall Z-0599-2016
NIPRO SafeTouch II Safety AVF Needle, 17G x 1 ¿ inch
- FDA Device
- Class III
- terminated
- Published 2016-01-13
On 2016-01-13 the FDA classified a Class III recall of NIPRO SafeTouch II Safety AVF Needle, 17G x 1 ¿ inch by Nipro Medical, citing device has the potential to have torn wings.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0599-2016 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2014-04-01 |
| Published | 2016-01-13 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Nipro Medical |
| Distribution | TN |
Product
NIPRO SafeTouch II Safety AVF Needle, 17G x 1 ¿ inch. Item code FS+173230BC.
Reason
Device has the potential to have torn wings.
Identifiers
| code_info | Model No.: FS+173230BC, Lot #14A22 and Lot #14A26. |
|---|
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-0599-2016%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.