Class III — Nipro Medical Corporation
| Recalling firm | NIPRO CORPORATION |
|---|---|
| Registered facility | View this company's 8 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class III |
| Status | Terminated |
| Reason | Device has the potential to have torn wings. |
| Product | NIPRO SafeTouch II Safety AVF Needle, 17G x 1 inch. Item code FS+173230BC. |
| Quantity | 160,000 pieces. |
| Distribution | US distribution including TN. |
| Initiated | 2014-04-01 |
| Classified | 2016-01-06 |
| Terminated | 2016-12-14 |
| Recall number | Z-0599-2016 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class III recall — Nipro Medical Corporation (Z-0599-2016).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/72707/
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