Recall archive / FDA device enforcement
Remington MEDICAL, Automatic Cutting Needle, 18ga (1.3mm) x 20cm, REF NAC-1820M (1) — FDA record Z-0771-2023
Reported terminated
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Dec 2, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- 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
- Classification
- Class II
- Recalling firm
- Remington Medical, Inc.
- Quantity
- 290 devices
- Agency-reported status
- Terminated
- Source record identifier
- Z-0771-2023
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | UDI/DI 00813079020936, Lot Number 2224920, exp. 2025-09/06 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
NC, WV, CA, PA, AL, TX
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Report date
- Jan 4, 2023
- Recall initiation date
- Dec 2, 2022
- Center classification date
- Dec 28, 2022
- Termination date
- Mar 16, 2026
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.