FDA Device recall Z-1834-2014
NIPRO Safe Touch Safety Scalp Vein Set
- FDA Device
- Class II
- terminated
- Published 2014-06-25
On 2014-06-25 the FDA classified a Class II recall of NIPRO Safe Touch Safety Scalp Vein Set by Nipro Medical, citing there is a possibility of a crack in the CP luer connector. The position of the crack is at the connection site of the CP luer connector and the tubing. The crack could cause or c….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1834-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-05-04 |
| Published | 2014-06-25 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Nipro Medical |
| Distribution | n/a |
Product
NIPRO Safe Touch Safety Scalp Vein Set
Reason
There is a possibility of a crack in the CP luer connector. The position of the crack is at the connection site of the CP luer connector and the tubing. The crack could cause or contribute to leakage of fluids.
Identifiers
| code_info | Product Code: PR+25G19, Lots #s 12H31H and 12I14H; Product Code: SPR+21G19, Lots #s 12I24 and 12J11; Product Code: PR…Product Code: PR+25G19, Lots #s 12H31H and 12I14H; Product Code: SPR+21G19, Lots #s 12I24 and 12J11; Product Code: PR-25G19, Lot # 12H27H; and PR-23G19, Lot # 12I12H. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
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FDA Device · Class II · 2016-01-20 · Nipro Medical - NIPRO SafeTouch II Safety AVF Needle, 17G x 1 ¿ inch
FDA Device · Class III · 2016-01-13 · Nipro Medical - 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 · 2015-11-04 · Nipro Medical
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1834-2014%22
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