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

Recall Z-1116-2020 — Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System

U.S. FDA — Device Enforcement · United States · 2020-01-09 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1116-2020
Date of alert
2020-01-09
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
TELEFLEX MEDICAL INC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
004551003
Reported risk: The products are being recalled due to reports of breakage broke at the point of a welded joint either prior to use during setup or during use inside the patient's mouth.
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.

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