Remington MEDICAL — Class II medical device recall Z-0771-2023
Terminated recall by Remington Medical, Inc., reported 2023-01-04, distributed in AL, CA, NC, PA, TX, WV. The stylet is longer than specified on the label
| Recall number | Z-0771-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Remington Medical, Inc., Alpharetta, GA, United States |
| Recall initiated | 2022-12-02 |
| Classified | 2022-12-28 |
| Reported by FDA | 2023-01-04 |
| Terminated | 2026-03-16 |
| Distributed | AL, CA, NC, PA, TX, WV |
| Quantity | 290 devices |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00813079020936 |
| Lot numbers | 2025-09/06, 2224920 |
| Model numbers | NAC-1820M |
Product
Remington MEDICAL, Automatic Cutting Needle, 18ga (1.3mm) x 20cm, REF NAC-1820M (1)
Reason for recall
The stylet is longer than specified on the label
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-0771-2023. 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.