Class II — Remington Medical, Inc.
| Recalling firm | REMINGTON MEDICAL, INC. |
|---|---|
| Registered facility | View this company's 3 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | The stylet is longer than specified on the label |
| Product | Remington MEDICAL, Automatic Cutting Needle, 18ga (1.3mm) x 20cm, REF NAC-1820M (1) |
| Quantity | 290 devices |
| Distribution | NC, WV, CA, PA, AL, TX |
| Initiated | 2022-12-02 |
| Classified | 2022-12-28 |
| Terminated | 2026-03-16 |
| Recall number | Z-0771-2023 |
| 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 — Remington Medical, Inc. (Z-0771-2023).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/91275/
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