Home / Import refusals / AV3-0022986-9/2/4

FDA Import Refusal AV3-0022986-9/2/4 — Covidien LLC

Covidien LLC — FEI 2936999

The FDA refused shipment AV3-0022986-9/2/4 from Covidien LLC (United States) on November 16, 2010. The refused product falls under Devices — NEEDLE, HYPODERMIC, SINGLE LUMEN. Cited charge: 118 This firm has 5 or more other import refusals on record.

Refusal Details

Date
November 16, 2010
Country
United States
Product Category
Devices
Product Code
80FMI NEEDLE, HYPODERMIC, SINGLE LUMEN
Charges
118

Recent inspections

  • 1260161 (NAI Wed Jul 16 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 917680 (VAI Thu Feb 26 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 659164 (NAI Thu Apr 22 2010 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 639004 (NAI Wed Jan 13 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • SCS-6646173-6/11/1 (Thu Nov 21 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-2601515-8/21/1 (Mon Oct 07 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 231-7179998-0/11/1 (Thu Mar 09 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-2389325-9/11/1 (Fri Dec 30 2022 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-8430821-2/21/1 (Thu Jul 14 2022 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources