FDA Medical Device Recalls (openFDA)
TELEFLEX MEDICAL INC: Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System
- Recall number
- Z-1117-2020
- Recalling firm
- TELEFLEX MEDICAL INC
- Product
- Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System
- Status
- Terminated
- Initiated
- 2020-01-09
- Posted
- 2020-02-07
- Terminated
- 2023-09-11
- Reason
- 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.
- Root cause
- Process control
- Action
- Letters sent to customers/users to immediately discontinue use and quarantine any products with the affected product code and lot numbers and return them to the manufacturer.
- 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
- Lot, serial or model codes
- Product Code 004551004; Lot Numbers 1812341, 1903341
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- CCW
- Firm FEI
- 3005747797
- Firm city
- Morrisville
- Firm state
- NC
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28