FDA Device recall Z-0771-2023
Remington MEDICAL, Automatic Cutting Needle, 18ga (1.3mm) x 20cm, REF NAC-1820M (1)
- FDA Device
- Class II
- terminated
- Published 2023-01-04
On 2023-01-04 the FDA classified a Class II recall of Remington MEDICAL, Automatic Cutting Needle, 18ga (1.3mm) x 20cm, REF NAC-1820M (1) by Remington Medical, citing the stylet is longer than specified on the label.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0771-2023 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-12-02 |
| Published | 2023-01-04 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Remington Medical |
| Distribution | AL, CA, NC, PA, TX, WV |
Product
Remington MEDICAL, Automatic Cutting Needle, 18ga (1.3mm) x 20cm, REF NAC-1820M (1)
Reason
The stylet is longer than specified on the label
Identifiers
| code_info | UDI/DI 00813079020936, Lot Number 2224920, exp. 2025-09/06 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0771-2023%22
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