Class II — 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 II |
| Status | Terminated |
| Reason | Some 1 1/4" needles were packaged and labeled in the 1" blister package. |
| 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. |
| Quantity | 50,000 pieces |
| Distribution | Indiana |
| Initiated | 2015-08-13 |
| Classified | 2015-10-23 |
| Terminated | 2017-10-13 |
| Recall number | Z-0161-2016 |
| 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 II recall — Nipro Medical Corporation (Z-0161-2016).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/72365/
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