Dsaart, LLC

Country not established FDA establishment FEI 3003897287

Devices: 0
Registrations: FDA
FDA recalls: 66 ongoing

No devices from this company are in the catalogue yet.

Company details

FDA FEI number: 3003897287
Address: 2950 Arrowhead Drive, Carson City, NV, 89706

FDA recalls6

Recalls are matched to the firm by name. FDA recall data as of 22 Oct 2026.

Recalls initiated per year

2017 0
2018 0
2019 0
2020 0
2021 0
2022 0
2023 0
2024 0
2025 6
2026 0

2025
- 26 Sep 2025 Z-0944-2026 Class II Ongoing Manufactured products deviated from established specifications and were distributed without obtaining the required FDA premarket approvals or clearances. Distribution: U.S.: AR, AZ, CA, CO, CT, DC, FL, GA, KY, IL, MA, MD, MI, MN, MS, NE, NJ, NY, OH, OK, PA, TX, UT, VA, WA, WI and Puerto…
  Full distribution text
  U.S.: AR, AZ, CA, CO, CT, DC, FL, GA, KY, IL, MA, MD, MI, MN, MS, NE, NJ, NY, OH, OK, PA, TX, UT, VA, WA, WI and Puerto Rico. O.U.S.: N/A
  Submission number: K021820
- 26 Sep 2025 Z-0945-2026 Class II Ongoing Manufactured products deviated from established specifications and were distributed without obtaining the required FDA premarket approvals or clearances. Distribution: U.S.: AR, AZ, CA, CO, CT, DC, FL, GA, KY, IL, MA, MD, MI, MN, MS, NE, NJ, NY, OH, OK, PA, TX, UT, VA, WA, WI and Puerto…
  Full distribution text
  U.S.: AR, AZ, CA, CO, CT, DC, FL, GA, KY, IL, MA, MD, MI, MN, MS, NE, NJ, NY, OH, OK, PA, TX, UT, VA, WA, WI and Puerto Rico. O.U.S.: N/A
  Submission number: K021839
- 26 Sep 2025 Z-0946-2026 Class II Ongoing Manufactured products deviated from established specifications and were distributed without obtaining the required FDA premarket approvals or clearances. Distribution: U.S.: AR, AZ, CA, CO, CT, DC, FL, GA, KY, IL, MA, MD, MI, MN, MS, NE, NJ, NY, OH, OK, PA, TX, UT, VA, WA, WI and Puerto…
  Full distribution text
  U.S.: AR, AZ, CA, CO, CT, DC, FL, GA, KY, IL, MA, MD, MI, MN, MS, NE, NJ, NY, OH, OK, PA, TX, UT, VA, WA, WI and Puerto Rico. O.U.S.: N/A
  Submission number: K021417
- 26 Sep 2025 Z-0947-2026 Class II Ongoing Manufactured products deviated from established specifications and were distributed without obtaining the required FDA premarket approvals or clearances. Distribution: U.S.: AR, AZ, CA, CO, CT, DC, FL, GA, KY, IL, MA, MD, MI, MN, MS, NE, NJ, NY, OH, OK, PA, TX, UT, VA, WA, WI and Puerto…
  Full distribution text
  U.S.: AR, AZ, CA, CO, CT, DC, FL, GA, KY, IL, MA, MD, MI, MN, MS, NE, NJ, NY, OH, OK, PA, TX, UT, VA, WA, WI and Puerto Rico. O.U.S.: N/A
  Submission number: K021419
- 26 Sep 2025 Z-0948-2026 Class II Ongoing Manufactured products deviated from established specifications and were distributed without obtaining the required FDA premarket approvals or clearances. Distribution: U.S.: AR, AZ, CA, CO, CT, DC, FL, GA, KY, IL, MA, MD, MI, MN, MS, NE, NJ, NY, OH, OK, PA, TX, UT, VA, WA, WI and Puerto…
  Full distribution text
  U.S.: AR, AZ, CA, CO, CT, DC, FL, GA, KY, IL, MA, MD, MI, MN, MS, NE, NJ, NY, OH, OK, PA, TX, UT, VA, WA, WI and Puerto Rico. O.U.S.: N/A
  Submission number: K021337
- 26 Sep 2025 Z-0949-2026 Class II Ongoing Manufactured products deviated from established specifications and were distributed without obtaining the required FDA premarket approvals or clearances. Distribution: U.S.: AR, AZ, CA, CO, CT, DC, FL, GA, KY, IL, MA, MD, MI, MN, MS, NE, NJ, NY, OH, OK, PA, TX, UT, VA, WA, WI and Puerto…
  Full distribution text
  U.S.: AR, AZ, CA, CO, CT, DC, FL, GA, KY, IL, MA, MD, MI, MN, MS, NE, NJ, NY, OH, OK, PA, TX, UT, VA, WA, WI and Puerto Rico. O.U.S.: N/A
  Submission number: K022511

This is an FDA establishment record without devices in deviCERTS.