Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1447-2020 — Kits containing Covidien Force TriVerse Electrosurgical Devices. Distributed in EMEA (Europe, Middle East, and Africa) only. No US distribution. Kits are manufactured in The Netherlands. Item codes BREASTKIT01 BREASTKIT01 BREASTKIT01 BREASTKIT01 BREASTKIT01 BREASTKIT01 BREASTKIT01 BREASTKIT01

U.S. FDA — Device Enforcement · United States · 2020-02-10 · Class II

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →

Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1447-2020
Date of alert: 2020-02-10
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Covidien Llc
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 0218917589

Reported risk: Sterile packaging may potentially be compromised, and use of products may result in increased risk for infection.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Related