FDAFDA · Food and drugs·Recall number Z-1117-2020
Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System
Published February 19, 2020 · Recall initiated: January 9, 2020
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- TELEFLEX MEDICAL INC
- Distributor
- Distributed nationwide in the US and to Puerto Rico; OUS to more than 20 countries; To the following government VA medical Centers: VAMC - KANSAS CITY MO 4801 E Linwood Blvd Kansas City MO 64128-2218
- Lot
- Product Code 004551004; Lot Numbers 1812341, 1903341
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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