Rusch Greenlite Single-Use Metal Laryngoscope Blade for recall
Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System
Why was Rusch Greenlite Single-Use Metal Laryngoscope Blade for recalled?
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 should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Product Code 004551004; Lot Numbers 1812341, 1903341
- Product
- Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System
- Recalling firm
- TELEFLEX MEDICAL INC
- Quantity
- 338,928 (199,018 US and 139,910 OUS) for all products
- Distribution
- 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
- Recall date
- February 19, 2020
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)