Recall Z-2731-2020— TELEFLEX MEDICAL INC
Class II · Terminated
Class II FDA medical device recall by TELEFLEX MEDICAL INC, initiated 2020-07-06, terminated 2023-08-31. FDA's recall record names no specific 510(k) clearance for this event. Product: Rusch Greenlite Product Code: 004551004 GTIN: 24026704553796 (each) - Product Usage: The laryngoscope is a device intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.. Reason: Breaking at the point of a welded joint.
- Recalling firm
- TELEFLEX MEDICAL INC
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2020-07-06
- Terminated
- 2023-08-31
- Firm location
- Morrisville, NC, United States
Product description
Rusch Greenlite Product Code: 004551004 GTIN: 24026704553796 (each) - Product Usage: The laryngoscope is a device intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.
Reason for recall
Breaking at the point of a welded joint
Data sourced from openFDA. This site is unofficial and independent of the FDA.