NIPRO SafeTouch II Safety AVF Needle — Class III medical device recall Z-0599-2016
Terminated recall by Nipro Medical Corporation, reported 2016-01-13, distributed in TN. Device has the potential to have torn wings.
| Recall number | Z-0599-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Nipro Medical Corporation, Miami, FL, United States |
| Recall initiated | 2014-04-01 |
| Classified | 2016-01-06 |
| Reported by FDA | 2016-01-13 |
| Terminated | 2016-12-14 |
| Distributed | TN |
| Quantity | 160,000 units |
| Lot numbers | 14A22, 14A26 |
Product
NIPRO SafeTouch II Safety AVF Needle, 17G x 1 ¿ inch. Item code FS+173230BC.
Reason for recall
Device has the potential to have torn wings.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0599-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.